Retinoic acid signaling and neuronal differentiation
Open accessAbstract
The identification of neurological symptoms caused by vitamin A deficiency pointed to a critical, early developmental role of vitamin A and its metabolite, retinoic acid (RA). The ability of RA to induce post-mitotic, neural phenotypes in various stem cells, in vitro, served as early evidence that RA is involved in the switch between proliferation and differentiation. In vivo studies have expanded this "opposing signal" model, and the number of primary neurons an embryo develops is now known to depend critically on the levels and spatial distribution of RA. The proneural and neurogenic transcription factors that control the exit of neural progenitors from the cell cycle and allow primary neurons to develop are partly elucidated, but the downstream effectors of RA receptor (RAR) signaling (many of which are putative cell cycle regulators) remain largely unidentified. The molecular mechanisms underlying RA-induced primary neurogenesis in anamniote embryos are starting to be revealed; however, these data have been not been extended to amniote embryos. There is growing evidence that bona fide RARs are found in some mollusks and other invertebrates, but little is known about their necessity or functions in neurogenesis. One normal function of RA is to regulate the cell cycle to halt proliferation, and loss of RA signaling is associated with dedifferentiation and the development of cancer. Identifying the genes and pathways that mediate cell cycle exit downstream of RA will be critical for our understanding of how to target tumor differentiation. Overall, elucidating the molecular details of RAR-regulated neurogenesis will be decisive for developing and understanding neural proliferation-differentiation switches throughout development.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Initial studies have used RA as a potent regulator of neural differentiation.
“Initial studies have used RA as a potent regulator of neural differentiation72.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [72]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Calcium's Role in Mechanotransduction during Muscle Development
Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,548 · see citing works
Rudin, W. (1973) · Cited by 13,708 · see citing works
CDK inhibitors: positive and negative regulators of G1-phase progression
Sherr, C. J., & Roberts, J. M. (1999) · Genes & Development · doi:10.1101/gad.13.12.1501 · Cited by 6,115 · see citing works
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases.
Wade Harper, J. (1993) · Cell · doi:10.1016/0092-8674(93)90499-g · Cited by 5,651 · see citing works
Reynolds, B. A., & Weiss, S. (1992) · Science · doi:10.1126/science.1553558 · Cited by 5,413 · see citing works
Identification of a cancer stem cell in human brain tumors.
Singh, S. K., Clarke, I. D., Terasaki, M., Bonn, V. E., Hawkins, C. E., Squire, J. A., & Dirks, P. B. (2003) · PubMed · Cited by 4,861 · see citing works
Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells
Boyer, L. A., Lee, T. I., Cole, M. F., Johnstone, S. E., Levine, S. S., Zucker, J. P., Guenther, M. G., Kumar, R. M., Murray, H. L., Jenner, R. G., et al. (2005) · Cell · doi:10.1016/j.cell.2005.08.020 · Cited by 4,505 · see citing works
Isolation and Characterization of Tumorigenic, Stem-like Neural Precursors from Human Glioblastoma
Galli, R., Binda, E., Orfanelli, U., Cipelletti, B., Gritti, A., Vitis, S. D., Fiocco, R., Foroni, C., DiMeco, F., & Vescovi, A. L. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-1364 · Cited by 2,570 · see citing works
The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells
Loh, Y., Wu, Q., Chew, J.-L., Vega, V. B., Zhang, W., Chen, X., Bourque, G., George, J., Leong, B., Liu, J., et al. (2006) · Nature Genetics · doi:10.1038/ng1760 · Cited by 2,438 · see citing works
Prediction of central nervous system embryonal tumour outcome based on gene expression
Pomeroy, S. L., Tamayo, P., Gaasenbeek, M., Sturla, L. M., Angelo, M., McLaughlin, M. E., Kim, J. Y. H., Goumnerova, L. C., Black, P. M., Lau, C. C., et al. (2002) · Nature · doi:10.1038/415436a · Cited by 2,369 · see citing works
Identification of a CpG Island Methylator Phenotype that Defines a Distinct Subgroup of Glioma
Noushmehr, H., Weisenberger, D. J., Diefes, K., Phillips, H. S., Pujara, K., Berman, B. P., Pan, F., Pelloski, C. E., Sulman, E. P., Bhat, K. P., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.03.017 · Cited by 2,337 · see citing works
A human retinoic acid receptor which belongs to the family of nuclear receptors
Petkovich, M., Brand, N. J., Krust, A., & Chambon, P. (1987) · Nature · doi:10.1038/330444a0 · Cited by 2,214 · see citing works
A Perivascular Niche for Brain Tumor Stem Cells
Calabrese, C. R., Poppleton, H., Koçak, M., Hogg, T. L., Fuller, C. E., Hamner, J. B., Oh, E. Y., Gaber, M. W., Finklestein, D., Allen, M., et al. (2007) · Cancer Cell · doi:10.1016/j.ccr.2006.11.020 · Cited by 2,203 · see citing works
G <sub>1</sub> Events and Regulation of Cell Proliferation
Pardee, A. B. (1989) · Science · doi:10.1126/science.2683075 · Cited by 2,182 · see citing works
Polyák, K., Lee, M.-H., Erdjument‐Bromage, H., Koff, A., Roberts, J. M., Tempst, P., & Massagué, J. (1994) · Cell · doi:10.1016/0092-8674(94)90572-x · Cited by 2,118 · see citing works
Rhodes, D. R., Sundaram, S. K., Mahavisno, V., Varambally, R., Yu, J., Briggs, B., Barrette, T. R., Anstett, M. J., Kincead-Beal, C., Kulkarni, P., et al. (2007) · Neoplasia · doi:10.1593/neo.07112 · Cited by 2,051 · see citing works
Multiclass cancer diagnosis using tumor gene expression signatures
Ramaswamy, S., Tamayo, P., Rifkin, R. M., Mukherjee, S., Yeang, C., Angelo, M., Ladd, C., Reich, M. M., Latulippe, É., Mesirov, J. P., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211566398 · Cited by 2,029 · see citing works
IDH1 mutation is sufficient to establish the glioma hypermethylator phenotype
Turcan, S., Rohle, D., Goenka, A., Walsh, L. A., Fang, F., Yilmaz, E., Campos, C., Fabius, A. W. M., Lu, C., Ward, P. S., et al. (2012) · Nature · doi:10.1038/nature10866 · Cited by 1,974 · see citing works
Identification of a receptor for the morphogen retinoic acid
Giguere, V., Ong, E. S., Segui, P., & Evans, R. M. (1987) · Nature · doi:10.1038/330624a0 · Cited by 1,965 · cited 1× · see citing works
“Shortly after the cloning of the first retinoic acid receptors (RARs) [12, 13], it was observed that the P19derived cell line, RAC65, was incapable of neuronal differentiation due to a 70-amino acid truncation in the RARa ligand-binding domain [14, 15].”
BackgroundCancerous stem cells can arise from pediatric brain tumors
Hemmati, H. D., Nakano, I., Lazareff, J. A., Masterman-Smith, M. D., Geschwind, D. H., Bronner-Fraser, M. E., & Kornblum, H. I. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2036535100 · Cited by 1,801 · see citing works
Control of cell cycle transcription during G1 and S phases
Bertoli, C., Skotheim, J. M., & de Bruin, R. A. M. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3629 · Cited by 1,509 · see citing works
Dulić, V., Kaufmann, W. K., Wilson, S. J., Tisty, T. D., Lees, E., Harper, J. W., Elledge, S. J., & Reed, S. I. (1994) · Cell · doi:10.1016/0092-8674(94)90379-4 · Cited by 1,465 · see citing works
Asymmetric and symmetric stem-cell divisions in development and cancer
Morrison, S. J., & Kimble, J. E. (2006) · Nature · doi:10.1038/nature04956 · Cited by 1,393 · see citing works
An inhibitor of mutant IDH1 delays growth and promotes differentiation of glioma cells
Rohle, D., Popovici-Muller, J., Palaskas, N., Turcan, S., Grommes, C., Campos, C., Tsoi, J., Clark, O., Oldrini, B., Komisopoulou, E., et al. (2013) · Science · doi:10.1126/science.1236062 · Cited by 1,153 · see citing works
Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state
Chaffer, C. L., Brueckmann, I., Scheel, C., Kaestli, A. J., Wiggins, P. A., Rodrigues, L. O., Brooks, M. W., Reinhardt, F., Su, Y., Polyák, K., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102454108 · Cited by 1,137 · see citing works
The ETS-domain transcription factor family
Sharrocks, A. D. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35099076 · Cited by 1,086 · see citing works
Intestinal Tumorigenesis Initiated by Dedifferentiation and Acquisition of Stem-Cell-like Properties
Schwitalla, S., Fingerle, A. A., Cammareri, P., Nebelsiek, T., Göktuna, S. İ., Ziegler, P. K., Canli, Ö., Heijmans, J., Huels, D. J., Moreaux, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.12.012 · Cited by 1,057 · see citing works
Increasing p16INK4a expression decreases forebrain progenitors and neurogenesis during ageing
Molofsky, A. V., Slutsky, S. G., Joseph, N. M., He, S., Pardal, R., Krishnamurthy, J., Sharpless, N. E., & Morrison, S. J. (2006) · Nature · doi:10.1038/nature05091 · Cited by 972 · cited 1× · see citing works
“Id1 also antagonizes a different CIK, p16 [161], which is found specifically in adult nervous tissue [162].”
BackgroundKip/Cip and Ink4 Cdk inhibitors cooperate to induce cell cycle arrest in response to TGF-beta.
Reynisdóttir, I., Polyak, K., Iavarone, A., & Massagué, J. (1995) · Genes & Development · doi:10.1101/gad.9.15.1831 · Cited by 962 · see citing works
Multipotent neural cell lines can engraft and participate in development of mouse cerebellum
Snyder, E. Y., Deitcher, D. L., Walsh, C. A., Arnold-Aldea, S. A., Hartwieg, E. A., & Cepko, C. L. (1992) · Cell · doi:10.1016/0092-8674(92)90204-p · Cited by 915 · see citing works
Id1 and Id3 are required for neurogenesis, angiogenesis and vascularization of tumour xenografts
Lyden, D. C., Young, A. Z., Zagzag, D., Yan, W. X., Gerald, W. L., O'Reilly, R., Bader, B., Hynes, R. O., Zhuang, Y., Manova, K., et al. (1999) · Nature · doi:10.1038/44334 · Cited by 912 · see citing works
Retinoic acid in the development, regeneration and maintenance of the nervous system
Maden, M. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2212 · Cited by 896 · see citing works
Retinoic acid signalling during development
Rhinn, M., & Dollé, P. (2012) · Development · doi:10.1242/dev.065938 · Cited by 849 · see citing works
The Molecular Basis of Visual Excitation
WALD, G. (1968) · Nature · doi:10.1038/219800a0 · Cited by 824 · see citing works
Encinas, M., Iglesias, M., Liu, Y., Wang, H., Muhaisen, A., Ceña, V., Gallego, C., & Comella, J. X. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0750991.x · Cited by 822 · see citing works
Dll1+ secretory progenitor cells revert to stem cells upon crypt damage
van Es, J. H., Sato, T., van de Wetering, M., Lyubimova, A., Nee, A. N. Y., Gregorieff, A., Sasaki, N., Zeinstra, L. M., van den Born, M., Korving, J., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2581 · Cited by 781 · see citing works
The promise of retinoids to fight against cancer
Altucci, L., & Gronemeyer, H. (2001) · Nature Reviews Cancer · doi:10.1038/35106036 · Cited by 773 · see citing works
Hemmati‐Brivanlou, A., Kelly, O., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90320-4 · Cited by 761 · see citing works
Lessard, J., Wu, J. I., Ranish, J. A., Wan, M., Winslow, M. M., Staahl, B. T., Wu, H., Aebersold, R., Graef, I. A., & Crabtree, G. R. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.019 · Cited by 735 · see citing works
Retinoic acid in development: Towards an integrated view
Niederreither, K., & Dollé, P. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2340 · Cited by 726 · see citing works
Kato, J., Matsuoka, M., Polyák, K., Massagué, J., & Sherr, C. J. (1994) · Cell · doi:10.1016/0092-8674(94)90257-7 · Cited by 720 · see citing works
Resurrecting the Ancestral Steroid Receptor: Ancient Origin of Estrogen Signaling
Thornton, J. W., Need, E. F., & Crews, D. P. (2003) · Science · doi:10.1126/science.1086185 · Cited by 700 · see citing works
Mosaic Analysis with Double Markers Reveals Tumor Cell of Origin in Glioma
Liu, C., Sage, J. C., Miller, M. R., Verhaak, R. G. W., Hippenmeyer, S., Vogel, H. S., Foreman, O., Bronson, R. T., Nishiyama, A., Luo, L., et al. (2011) · Cell · doi:10.1016/j.cell.2011.06.014 · Cited by 692 · see citing works
Molecular biology of the Ets family of transcription factors
Oikawa, T., & Yamada, T. (2003) · Gene · doi:10.1016/s0378-1119(02)01156-3 · Cited by 684 · see citing works
Schug, T. T., Berry, D. C., Shaw, N. S., Travis, S. N., & Noy, N. (2007) · Cell · doi:10.1016/j.cell.2007.02.050 · Cited by 680 · see citing works
Dedifferentiation of committed epithelial cells into stem cells in vivo
Tata, P. R., Mou, H., Pardo–Saganta, A., Zhao, R., Prabhu, M., Law, B. M., Vinarsky, V., Cho, J. L., Breton, S., Sahay, A., et al. (2013) · Nature · doi:10.1038/nature12777 · Cited by 657 · see citing works
Opposing effects of Ets and Id proteins on p16INK4a expression during cellular senescence
Ohtani, N., Zebedee, Z., Huot, T. J. G., Stinson, J. A., Sugimoto, M., Ohashi, Y., Sharrocks, A. D., Peters, G., & Hara, E. (2001) · Nature · doi:10.1038/35059131 · Cited by 654 · see citing works
Thiele, C. J., Reynolds, C. P., & Israel, M. A. (1985) · Nature · doi:10.1038/313404a0 · Cited by 649 · see citing works
Retinoic acid induces embryonal carcinoma cells to differentiate into neurons and glial cells.
Jones-Villeneuve, E. M., McBurney, M. W., Rogers, K. A., & Kalnins, V. I. (1982) · The Journal of cell biology · doi:10.1083/jcb.94.2.253 · Cited by 645 · see citing works
Osakada, F., Ikeda, H. O., Mandai, M., Wataya, T., Watanabe, K., Yoshimura, N., Akaike, A., Sasai, Y., & Takahashi, M. (2008) · Nature Biotechnology · doi:10.1038/nbt1384 · Cited by 629 · see citing works
del Corral, R. D., Olivera-Martínez, I., Goriely, A., Gale, E. A., Maden, M., & Storey, K. G. (2003) · Neuron · doi:10.1016/s0896-6273(03)00565-8 · Cited by 605 · see citing works
Evolution of Hormone-Receptor Complexity by Molecular Exploitation
Bridgham, J. T., Carroll, S. M., & Thornton, J. W. (2006) · Science · doi:10.1126/science.1123348 · Cited by 601 · see citing works
Weissman, T. A., Riquelme, P. A., Ivic, L., Flint, A. C., & Kriegstein, A. R. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.015 · Cited by 579 · see citing works
Dedifferentiation of Neurons and Astrocytes by Oncogenes Can Induce Gliomas in Mice
Friedmann‐Morvinski, D., Bushong, E. A., Ke, E., Soda, Y., Marumoto, T., Singer, O., Ellisman, M. H., & Verma, I. M. (2012) · Science · doi:10.1126/science.1226929 · Cited by 566 · see citing works
Id family of helix-loop-helix proteins in cancer
Perk, J., Iavarone, A., & Benezra, R. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1673 · Cited by 535 · see citing works
Knoepfler, P. S., Cheng, P. F., & Eisenman, R. N. (2002) · Genes & Development · doi:10.1101/gad.1021202 · Cited by 520 · see citing works
Cell cycle regulation in the postmitotic neuron: oxymoron or new biology?
Herrup, K., & Yang, Y. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2124 · Cited by 507 · see citing works
Regulation of Cell Cycle Progression by Calcium/Calmodulin-Dependent Pathways
Kahl, C. R., & Means, A. R. (2003) · Endocrine Reviews · doi:10.1210/er.2003-0008 · Cited by 493 · see citing works
Inhibition of activin receptor signaling promotes neuralization in Xenopus
Hemmati‐Brivanlou, A., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90319-0 · Cited by 491 · see citing works
Dedifferentiation and reprogramming: origins of cancer stem cells
Friedmann‐Morvinski, D., & Verma, I. M. (2014) · EMBO Reports · doi:10.1002/embr.201338254 · Cited by 488 · see citing works
The Human Tumor Antigen PRAME Is a Dominant Repressor of Retinoic Acid Receptor Signaling
Epping, M. T., Wang, L., Edel, M. J., Carlée, L., Hernandez, M., & Bernards, R. (2005) · Cell · doi:10.1016/j.cell.2005.07.003 · Cited by 432 · see citing works
Retinoid signalling in the development of the central nervous system
Maden, M. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn963 · Cited by 428 · see citing works
Neural induction: old problem, new findings, yet more questions
Stern, C. D. (2005) · Development · doi:10.1242/dev.01794 · Cited by 421 · cited 1× · see citing works
“Curiously, this result has not been followed up despite its interest to the field [150].”
BackgroundDivision and differentiation of isolated CNS blast cells in microculture
Temple, S. (1989) · Nature · doi:10.1038/340471a0 · Cited by 412 · see citing works
Retinoic acid from the meninges regulates cortical neuron generation.
Siegenthaler, J. A., Ashique, A. M., Zarbalis, K., Patterson, K. P., Hecht, J. H., Kane, M. A., Folias, A. E., Choe, Y., May, S. R., Kume, T., et al. (2009) · Cell · doi:10.1016/j.cell.2009.10.004 · Cited by 402 · see citing works
Castro, D. S., Martynoga, B., Parras, C. M., Ramesh, V., Pacary, E., Johnston, C., Drechsel, D., Lebel, M., Garcia, L. G., Hunt, C., et al. (2011) · Genes & Development · doi:10.1101/gad.627811 · Cited by 396 · see citing works
Sidell, N. (1982) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/68.4.589 · Cited by 378 · see citing works
Vitamin A-deficient quail embryos have half a hindbrain and other neural defects.
Maden, M., Gale, E., Kostetskii, I., & Zile, M. (1996) · Current Biology · doi:10.1016/s0960-9822(02)00509-2 · Cited by 351 · see citing works
FGF signalling: diverse roles during early vertebrate embryogenesis
Dorey, K., & Amaya, E. (2010) · Development · doi:10.1242/dev.037689 · Cited by 341 · see citing works
N-myc can functionally replace c-myc in murine development, cellular growth, and differentiationPreprint
Malynn, B. A., de Alborán, I. M., O’Hagan, R. C., Bronson, R. T., Davidson, L., DePinho, R. A., & Alt, F. W. (2000) · Genes & Development · doi:10.1101/gad.14.11.1390 · Cited by 331 · see citing works
Nishikawa, J., Mamiya, S., Kanayama, T., Nishikawa, T., Shiraishi, F., & Horiguchi, T. (2004) · Environmental Science & Technology · doi:10.1021/es049593u · Cited by 322 · see citing works
Sidell, N., Altman, A., Haussler, M. R., & Seeger, R. C. (1983) · Experimental Cell Research · doi:10.1016/0014-4827(83)90184-2 · Cited by 318 · see citing works
Distinct roles for Fgf, Wnt and retinoic acid in posteriorizing the neural ectoderm
Kudoh, T., Wilson, S. W., & Dawid, I. B. (2002) · Development · doi:10.1242/dev.129.18.4335 · Cited by 302 · see citing works
Degradation of Id2 by the anaphase-promoting complex couples cell cycle exit and axonal growth
Lasorella, A., Stegmüller, J., Guardavaccaro, D., Liu, G., Carro, M. S., Rothschild, G., de la Torre-Ubieta, L., Pagano, M., Bonni, A., & Iavarone, A. (2006) · Nature · doi:10.1038/nature04895 · Cited by 298 · see citing works
Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition
Delaune, E. A., Lemaire, P., & Kodjabachian, L. (2004) · Development · doi:10.1242/dev.01582 · Cited by 290 · see citing works
The BRG1 transcriptional coregulator
Trotter, K. W., & Archer, T. (2008) · Nuclear Receptor Signaling · doi:10.1621/nrs.06004 · Cited by 287 · see citing works
On the epigenetic regulation of the human reelin promoter
Chen, Y. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf401 · Cited by 274 · see citing works
Retinoic acid promotes differentiation of photoreceptors in vitro
Kelley, M. W., Turner, J. K., & Reh, T. A. (1994) · Development · doi:10.1242/dev.120.8.2091 · Cited by 273 · see citing works
Cell cycle control of mammalian neural stem cells: putting a speed limit on G1
Salomoni, P., & Calegari, F. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.01.006 · Cited by 272 · see citing works
Retinoic acid is required early during adult neurogenesis in the dentate gyrus
Jacobs, S. G. P. M., Lie, D. C., DeCicco-Skinner, K. L., Shi, Y., DeLuca, L. M., Gage, F. H., & Evans, R. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511294103 · Cited by 259 · see citing works
Cell cycle regulation and neural differentiation
Galderisi, U., Jori, F. P., & Giordano, A. (2003) · Oncogene · doi:10.1038/sj.onc.1206558 · Cited by 248 · see citing works
An essential role for retinoid signaling in anteroposterior neural patterning
Blumberg, B., Bolado, J., Moreno, T. A., Kintner, C. R., Evans, R. M., & Papalopulu, N. (1997) · Development · doi:10.1242/dev.124.2.373 · Cited by 239 · see citing works
Self-citationGli/Zic factors pattern the neural plate by defining domains of cell differentiation
Brewster, R. M., Lee, J. D., & Altaba, A. R. I. (1998) · Nature · doi:10.1038/31242 · Cited by 234 · see citing works
Grunz, H., & Tacke, L. (1989) · Cell Differentiation and Development · doi:10.1016/0922-3371(89)90006-3 · Cited by 233 · see citing works
Hölzel, M., Huang, S., Köster, J., Øra, I., Lakeman, A., Caron, H. N., Nijkamp, W., Xie, J., Callens, T., Asgharzadeh, S., et al. (2010) · Cell · doi:10.1016/j.cell.2010.06.004 · Cited by 225 · see citing works
Ninkovic, J., Steiner-Mezzadri, A., Jawerka, M., Akinci, U., Masserdotti, G., Petricca, S., Fischer, J., von Holst, A., Beckers, J., Lie, D. C., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.07.002 · Cited by 208 · see citing works
Hartenstein, V. (1989) · Neuron · doi:10.1016/0896-6273(89)90200-6 · Cited by 207 · see citing works
Regulation of glioblastoma stem cells by retinoic acid: role for Notch pathway inhibition
Ying, M., Wang, S., Sang, Y., Sun, P., Lal, B., Goodwin, C. R., Guerrero-Cazares, H., Quinones-Hinojosa, A., Laterra, J., & Xia, S. (2011) · Oncogene · doi:10.1038/onc.2011.58 · Cited by 204 · see citing works
McCaffery, P. J. A., Adams, J., Maden, M., & Rosa‐Molinar, E. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02765.x · Cited by 201 · see citing works
Hale, F. (1933) · Springer eBooks · doi:10.1007/978-94-011-6621-8_21 · Cited by 199 · see citing works
BMP-2 mediates retinoid-induced apoptosis in medulloblastoma cells through a paracrine effect
Hallahan, A. R., Pritchard, J. I., Chandraratna, R. A. S., Ellenbogen, R. G., Geyer, J. R., Overland, R. P., Strand, A. D., Tapscott, S. J., & Olson, J. M. (2003) · Nature Medicine · doi:10.1038/nm904 · Cited by 192 · see citing works
Ling, F., Kang, B., & Sun, X.-H. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-405943-6.00005-1 · Cited by 191 · see citing works
Distinct human NUMB isoforms regulate differentiation vs. proliferation in the neuronal lineage
Verdi, J. M., Bashirullah, A., Goldhawk, D. E., Kubu, C. J., Jamali, M., Meakin, S. O., & Lipshitz, H. D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10472 · Cited by 188 · see citing works
Seo, S., Richardson, G. A., & Kroll, K. L. (2004) · Development · doi:10.1242/dev.01548 · Cited by 187 · see citing works
The first neurons of the human cerebral cortex
Bystron, I., Rakic, P., Molnár, Z., & Blakemore, C. (2006) · Nature Neuroscience · doi:10.1038/nn1726 · Cited by 183 · see citing works
Ali, F. R., Hindley, C., McDowell, G. S., Deibler, R. W., Jones, A., Kirschner, M. W., Guillemot, F., & Philpott, A. (2011) · Development · doi:10.1242/dev.067900 · Cited by 181 · see citing works
Geminin regulates neuronal differentiation by antagonizing Brg1 activityPreprint
Seo, S., Herr, A., Lim, J.-W., Richardson, G. A., Richardson, H. E., & Kroll, K. L. (2005) · Genes & Development · doi:10.1101/gad.1319105 · Cited by 178 · see citing works
Cellular Strategies of Axonal PathfindingPreprint
Raper, J. A., & Mason, C. A. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001933 · Cited by 177 · see citing works
Retinoic acid establishes ventral retinal characteristics
Hyatt, G. A., Schmitt, E. A., Marsh-Armstrong, N., McCaffery, P. J. A., Dräger, U. C., & Dowling, J. E. (1996) · Development · doi:10.1242/dev.122.1.195 · Cited by 177 · see citing works
Lotan, R., & Nicolson, G. L. (1977) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/59.6.1717 · Cited by 176 · see citing works
Hale, F. (1933) · Journal of Heredity · doi:10.1093/oxfordjournals.jhered.a103720 · Cited by 176 · see citing works
Oberthuer, A., Hero, B., Spitz, R., Berthold, F., & Fischer, M. (2004) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-03-0813 · Cited by 175 · see citing works
Schug, T. T., Berry, D. C., Toshkov, I. A., Cheng, L., Nikitin, A. Y., & Noy, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709981105 · Cited by 172 · see citing works
Castro, L. F. C., Lima, D., Machado, A., Melo, C. A., Hiromori, Y., Nishikawa, J., Nakanishi, T., Reis-Henriques, M. A., & Santos, M. M. (2007) · Aquatic Toxicology · doi:10.1016/j.aquatox.2007.07.016 · Cited by 171 · see citing works
Sgouras, D. N., Athanasiou, M., Beal, G., Fisher, R. J., Blair, D. G., & Mavrothalassitis, G. J. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00160.x · Cited by 169 · see citing works
Origins of neurogenesis, a cnidarian view
Galliot, B., Quiquand, M., Ghila, L., de Rosa, R., Miljkovic-Licina, M., & Chera, S. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.05.563 · Cited by 168 · see citing works
Retinoic Acid-responsive Enhancers Located 3ʹ of the Hox A and Hox B Homeobox Gene Clusters
Langston, A. W., Thompson, J. R., & Gudas, L. J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.4.2167 · Cited by 165 · see citing works
A Mechanism Regulating the Onset of Sox2 Expression in the Embryonic Neural Plate
Papanayotou, C., Mey, A., Birot, A., Saka, Y., Boast, S., Smith, J. C., Samarut, J., & Stern, C. D. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060002 · Cited by 163 · see citing works
Papalopulu, N., & Kintner, C. R. (1996) · Development · doi:10.1242/dev.122.11.3409 · Cited by 162 · see citing works
Retinoic acid and hindbrain patterning
Glover, J. C., Renaud, J., & Rijli, F. M. (2006) · Journal of Neurobiology · doi:10.1002/neu.20272 · Cited by 145 · see citing works
Huang, S., Laoukili, J., Epping, M. T., Köster, J., Hölzel, M., Westerman, B. A., Nijkamp, W., Hata, A., Asgharzadeh, S., Seeger, R. C., et al. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.02.023 · Cited by 145 · see citing works
Ahmed, M. U., Xu, J., & Xu, P. (2012) · Development · doi:10.1242/dev.071670 · Cited by 143 · see citing works
Retinoic acid signaling and the evolution of chordates
Marlétaz, F., Holland, L. Z., Laudet, V., & Schubert, M. (2006) · International Journal of Biological Sciences · doi:10.7150/ijbs.2.38 · Cited by 141 · see citing works
Zic3 Is Required for Maintenance of Pluripotency in Embryonic Stem Cells
Lim, L. S., Loh, Y., Zhang, W., Li, Y., Chen, X., Wang, Y., Bakre, M. M., Ng, H., & Stanton, L. W. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-07-0624 · Cited by 141 · see citing works
Emerging roles for zic genes in early development
Merzdorf, C. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21098 · Cited by 140 · see citing works
The cdk inhibitor p27Xic1 is required for differentiation of primary neurones inXenopus
Vernon, A. E., Devine, C., & Philpott, A. (2002) · Development · doi:10.1242/dev.00193 · Cited by 137 · see citing works
Retinoic acid signaling in development: Tissue‐specific functions and evolutionary origins
Campo‐Paysaa, F., Marlétaz, F., Laudet, V., & Schubert, M. (2008) · genesis · doi:10.1002/dvg.20444 · Cited by 136 · see citing works
BMP inhibition initiates neural induction via FGF signaling and Zic genes
Marchal, L., Luxardi, G., Thomé, V., & Kodjabachian, L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906352106 · Cited by 135 · see citing works
Pratt, M. A. C., Králová, J., & McBurney, M. W. (1990) · Molecular and Cellular Biology · doi:10.1128/mcb.10.12.6445 · Cited by 133 · see citing works
Aruga, J., Tohmonda, T., Homma, S., & Mikoshiba, K. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0598 · Cited by 127 · see citing works
Meseguer, S., Mudduluru, G., Escamilla, J. M., Allgayer, H., & Barettino, D. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.167817 · Cited by 127 · see citing works
Id4regulates neural progenitor proliferation and differentiation in vivo
Yun, K., Mantani, A., Garel, S., Rubenstein, J. L. R., & Israel, M. A. (2004) · Development · doi:10.1242/dev.01430 · Cited by 126 · see citing works
Retinoic acid signaling and the evolution of chordates
Marlétaz, F., Holland, L. Z., Laudet, V., & Schubert, M. (2006) · Europe PMC (PubMed Central) · Cited by 123 · see citing works
Treatment of recurrent malignant gliomas with high-dose 13-cis-retinoic acid.
Yung, W. K. A., Kyritsis, A. P., Gleason, M. J., & Levin, V. A. (1996) · PubMed · Cited by 122 · see citing works
Risk of ovarian carcinoma and consumption of vitamins A, C, and E and specific carotenoids
Fairfield, K. M., Hankinson, S. E., ROSNER, B. A., Hunter, D. J., Colditz, G. A., & Willett, W. C. (2001) · Cancer · doi:10.1002/1097-0142(20011101)92:9 · Cited by 121 · see citing works
Antagonism between Retinoic Acid and Fibroblast Growth Factor Signaling during Limb Development
Cunningham, T. J., Zhao, X., Sandell, L. J., Evans, S. Μ., Trainor, P. A., & Duester, G. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.03.036 · Cited by 120 · see citing works
Kolm, P. J., & Sive, H. L. (1995) · Developmental Biology · doi:10.1006/dbio.1995.1005 · Cited by 117 · see citing works
Donato, L. J., Suh, J. H., & Noy, N. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-0989 · Cited by 116 · see citing works
Origin and evolution of the ligand-binding ability of nuclear receptors
Markov, G. V., & Laudet, V. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.10.017 · Cited by 113 · see citing works
Das, S., Foley, N. H., Bryan, K. R., Watters, K. M., Bray, I. M., Murphy, D. M., Buckley, P. G., & Stallings, R. L. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-1534 · Cited by 112 · see citing works
Protein kinase C mediates neural induction in Xenopus laevis
Otte, A. P., Koster, C. H., Snoek, G. T., & Durston, A. J. (1988) · Nature · doi:10.1038/334618a0 · Cited by 112 · see citing works
Cañestro, C., Bassham, S., & Postlethwait, J. H. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.06.039 · Cited by 109 · see citing works
Protein kinase C isozymes have distinct roles in neural induction and competence in Xenopus
Otte, A. P., & Moon, R. T. (1992) · Cell · doi:10.1016/0092-8674(92)90074-m · Cited by 107 · see citing works
Jager, M., Chiori, R., Alié, A., Dayraud, C., Quéinnec, E., & Manuel, M. (2011) · Journal of Experimental Zoology Part B: Molecular and Developmental Evolution · doi:10.1002/jez.b.21386 · Cited by 107 · see citing works
Complete inhibition of Cdk/cyclin by one molecule of p21Cip1Preprint
Hengst, L., Göpfert, U., Lashuel, H. A., & Reed, S. I. (1998) · Genes & Development · doi:10.1101/gad.12.24.3882 · Cited by 107 · see citing works
Neural induction is mediated by cross-talk between the protein kinase C and cyclic AMP pathways
Otte, A. P., van Run, P., Heideveld, M., DRIEL, R. V., & Durston, A. J. (1989) · Cell · doi:10.1016/0092-8674(89)90099-8 · Cited by 106 · see citing works
An Induced Ets Repressor Complex Regulates Growth Arrest during Terminal Macrophage Differentiation
Klappacher, G., Lunyak, V. V., Sykes, D. B., Sawka‐Verhelle, D., Sage, J., Brard, G., Ngo, S. D., Gangadharan, D., Jacks, T., Kamps, M. P., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)00714-6 · Cited by 106 · see citing works
Retinoic acid and the control of dorsoventral patterning in the avian spinal cord
Wilson, L., Gale, E. A., Chambers, D. J., & Maden, M. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.01.034 · Cited by 105 · see citing works
Cloning and characterization of the Xenopus cyclin-dependent kinase inhibitor p27XIC1.
Su, J. Y., Rempel, R. E., ERIKSON, E., & Maller, J. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10187 · Cited by 104 · see citing works
Longo, A., Guanga, G. P., & Rose, R. B. (2007) · Biochemistry · doi:10.1021/bi701527r · Cited by 104 · see citing works
Kee, Y., & Bronner-Fraser, M. E. (2005) · Genes & Development · doi:10.1101/gad.1257405 · Cited by 102 · see citing works
Horiguchi, T. (2006) · PubMed · Cited by 102 · see citing works
The calcium: an early signal that initiates the formation of the nervous system during embryogenesis
Leclerc, C., Néant, I., & Moreau, M. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00064 · Cited by 100 · see citing works
The nervous system of hydra. I. Types, distribution and origin of nerve elements
Burnett, A. L., & Diehl, N. A. (1964) · Journal of Experimental Zoology · doi:10.1002/jez.1401570205 · Cited by 99 · see citing works
Ebert, P. J., Timmer, J. R., Nakada, Y., Helms, A. W., Parab, P., Liu, Y. M., Hunsaker, T., & Johnson, J. E. B. (2003) · Development · doi:10.1242/dev.00419 · Cited by 97 · see citing works
Mitsuhashi, T., Aoki, Y., Ekşioğlu, Y. Z., Takahashi, T., Bhide, P. G., Reeves, S. A., & Caviness, V. S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111051398 · Cited by 97 · see citing works
Chalmers, A. D., Welchman, D. P., & Papalopulu, N. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00113-2 · Cited by 94 · see citing works
Neuronatin Promotes Neural Lineage in ESCs via Ca2+ Signaling
Lin, H., Bell, E. J. D. H., Uwanogho, D., Perfect, L., Noristani, H. N., Bates, T. J. D., Snetkov, V. A., Price, J., & Sun, Y.-M. (2010) · Stem Cells · doi:10.1002/stem.530 · Cited by 91 · see citing works
Matsuo, T., & Thiele, C. J. (1998) · Oncogene · doi:10.1038/sj.onc.1201830 · Cited by 89 · see citing works
Kuff, E. L., & Fewell, J. W. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90459-5 · Cited by 88 · see citing works
Cyclin-dependent kinase inhibitors in the development of the central nervous system.
Cunningham, J. J., & Roussel, M. F. (2001) · PubMed · Cited by 88 · see citing works
Functional association of retinoic acid and hedgehog signaling in Xenopus primary neurogenesis
Franco, P. G., Paganelli, A. R., López, S. L., & Carrasco, A. E. (1999) · Development · doi:10.1242/dev.126.19.4257 · Cited by 87 · see citing works
Wu, P., Lin, Y.-C., Chang, C.-L., Lu, H.-T., Chin, C.-H., Hsu, T., Chu, D., & Sun, S. H. (2009) · Cellular Signalling · doi:10.1016/j.cellsig.2009.01.036 · Cited by 86 · see citing works
Campos, B., Centner, F.-S., Bermejo, J. L., Ali, R., Dorsch, K., Wan, F., Felsberg, J., Ahmadi, R., Grabe, N., Reifenberger, G., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.01.051 · Cited by 86 · see citing works
Reelin-deficient mice show impaired neurogenesis and increased stroke size
Won, S. J., Kim, S. H., Xie, L., Wang, Y., Mao, X. O., Jin, K., & Greenberg, D. A. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2005.12.008 · Cited by 84 · see citing works
Neural induction and factors that stabilize a neural fate
Rogers, C. D., Moody, S. A., & Casey, E. S. (2009) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20157 · Cited by 84 · see citing works
Is retinoic acid genetic machinery a chordate innovation?
Cañestro, C., Postlethwait, J. H., Gonzàlez‐Duarte, R., & Albalat, R. (2006) · Evolution & Development · doi:10.1111/j.1525-142x.2006.00113.x · Cited by 83 · see citing works
Dual Control of Neurogenesis by PC3 through Cell Cycle Inhibition and Induction of Math1
Canzoniere, D., Vecchioli, S. F., Conti, F., Ciotti, M. T., Tata, A. M., Augusti-Tocco, G., Mattei, E., Lakshmana, M. K., Krizhanovsky, V., Reeves, S. A., et al. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3860-03.2004 · Cited by 83 · see citing works
Rogers, C. D., Harafuji, N., Archer, T. C., Cunningham, D. D., & Casey, E. S. (2008) · Mechanisms of Development · doi:10.1016/j.mod.2008.10.005 · Cited by 82 · see citing works
The retinoic acid machinery in invertebrates: Ancestral elements and vertebrate innovations
Albalat, R. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.08.029 · Cited by 82 · see citing works
Albalat, R., & Cañestro, C. (2008) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2008.09.017 · Cited by 81 · see citing works
On the ‘Discovery’ of Vitamin A
Semba, R. D. (2012) · Annals of Nutrition and Metabolism · doi:10.1159/000343124 · Cited by 80 · see citing works
E Proteins and Id2 Converge on p57Kip2 To Regulate Cell Cycle in Neural Cells
Rothschild, G., Zhao, X., Iavarone, A., & Lasorella, A. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01743-05 · Cited by 80 · see citing works
Increased internal Ca2+ mediates neural induction in the amphibian embryo.
Moreau, M., Leclerc, C., Gualandris, L., & Duprat, A. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.26.12639 · Cited by 78 · see citing works
Retinoid receptors promote primary neurogenesis in Xenopus
Sharpe, C. R., & Goldstone, K. (1997) · Development · doi:10.1242/dev.124.2.515 · Cited by 78 · see citing works
Corepressor Recruitment by Agonist-Bound Nuclear Receptors
White, J. H., Fernandes, I., Mader, S., & Yang, X. (2004) · Vitamins and hormones · doi:10.1016/s0083-6729(04)68004-6 · Cited by 77 · see citing works
Wald, G. (1933) · Nature · doi:10.1038/132316a0 · Cited by 77 · see citing works
Primordial neurosecretory apparatus identified in the choanoflagellate Monosiga brevicollis
Burkhardt, P., Stegmann, C. M., Cooper, B. H., Kloepper, T. H., Imig, C., Varoqueaux, F., Wahl, M. C., & Fasshauer, D. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106189108 · Cited by 77 · see citing works
Dedifferentiation of Neurons Precedes Tumor Formation in lola Mutants
Southall, T. D., Davidson, C. M., Miller, C., Carr, A. R., & Brand, A. H. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.01.030 · Cited by 75 · see citing works
Stallings, R. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209787315837 · Cited by 74 · see citing works
ERF Nuclear Shuttling, a Continuous Monitor of Erk Activity That Links It to Cell Cycle Progression
Gallic, L. L., Virgilio, L., Cohen, P., Biteau, B., & Mavrothalassitis, G. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.3.1206-1218.2004 · Cited by 73 · see citing works
Cuende, J., Moreno, S., Bolaños, J. P., & Almeida, Á. (2008) · Oncogene · doi:10.1038/sj.onc.1210987 · Cited by 70 · see citing works
el-Ghissassi, F., Valsesia‐Wittmann, S., Falette, N., Duriez, C., Walden, P. D., & Puisieux, A. (2002) · Oncogene · doi:10.1038/sj.onc.1205888 · Cited by 70 · see citing works
13-cis-Retinoic acid in the treatment of recurrent glioblastoma multiforme
See, S.-J., Levin, V. A., Yung, W.-K. A., Hess, K. R., & Groves, M. D. (2004) · Neuro-Oncology · doi:10.1215/s1152851703000607 · Cited by 69 · see citing works
Dmetrichuk, J. M., Carlone, R. L., Jones, T. R. B., Vesprini, N. D., & Spencer, G. E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3192-08.2008 · Cited by 69 · see citing works
Wullimann, M. F., Rink, E., Vernier, P., & Schlosser, G. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20634 · Cited by 68 · see citing works
Carruthers, S. N., Mason, J., & Papalopulu, N. (2003) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00010-8 · Cited by 68 · see citing works
XPak3 promotes cell cycle withdrawal during primary neurogenesis in Xenopus laevis
Souopgui, J., Sölter, M., & Pieler, T. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf644 · Cited by 67 · see citing works
The different roles of serum and calcium in the control of proliferation of BALB/C 3T3 mouse cells
Boynton, A. L., Whitfield, J. F., & Isaacs, R. J. (1976) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02796358 · Cited by 65 · see citing works
Passeri, D., Marcucci, A., Rizzo, G., Billi, M., Panigada, M., Leonardi, L., Tirone, F., & Grignani, F. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01360-05 · Cited by 64 · see citing works
Targeting Neuroblastoma Stem Cells with Retinoic Acid and Proteasome Inhibitor
Hämmerle, B., Yáñez, Y., Palanca, S., Cañete, A., Burks, D. J., Castel, V., & de Mora, J. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076761 · Cited by 64 · see citing works
Preclinical Models of Pediatric Solid Tumors (Neuroblastoma) and Their Use in Drug Discovery
Patterson, D., Shohet, J., & Kim, E. S. (2011) · Current Protocols in Pharmacology · doi:10.1002/0471141755.ph1417s52 · Cited by 63 · see citing works
Leclerc, C., Daguzan, C., Nicolas, M., Chabret, C., Duprat, A., & Moreau, M. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(97)00054-3 · Cited by 63 · see citing works
Chou, A. P., Chowdhury, R., Li, S., Chen, W., Kim, A. J., Piccioni, D. E., Selfridge, J. M., Mody, R. R., Chang, S., Lalezari, S., et al. (2012) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djs357 · Cited by 63 · see citing works
Georgopoulou, N., Hurel, C., Politis, P. K., Gaitanou, M., Matsas, R., & Thomaidou, D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602689200 · Cited by 62 · see citing works
Su, D., & Gudas, L. J. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.11.006 · Cited by 61 · see citing works
Coyle, D. E., Li, J., & Baccei, M. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016174 · Cited by 59 · see citing works
Eguren, M., Porlan, E., Manchado, E., García-Higuera, I., Cañamero, M., Fariñas, I., & Malumbres, M. (2013) · Nature Communications · doi:10.1038/ncomms3880 · Cited by 57 · see citing works
The treatment of recurrent cerebral gliomas with all-trans-retinoic acid (tretinoin)
Kaba, S. E., Kyritsis, A. P., Conrad, C. A., Gleason, M. J., Newman, R. A., Levin, V. A., & Yung, W. K. A. (1997) · Journal of Neuro-Oncology · doi:10.1023/a:1005743707803 · Cited by 56 · see citing works
Semmler, H., Chiodin, M., Bailly, X., Martı́nez, P., & Wanninger, A. (2010) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2010.01207.x · Cited by 55 · see citing works
Global analysis of RAR‐responsive genes in the Xenopus neurula using cDNA microarrays
Arima, K., Shiotsugu, J., Niu, R., Khandpur, R., Martinez, M., Shin, Y., Koide, T., Cho, K. W. Y., Kitayama, A., Ueno, N., et al. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20231 · Cited by 55 · see citing works
Self-citationA Mollusk Retinoic Acid Receptor (RAR) Ortholog Sheds Light on the Evolution of Ligand Binding
Gutierrez-Mazariegos, J., Nadendla, E. K., Lima, D., Pierzchalski, K., Jones, J. W., Kane, M. A., Nishikawa, J., Hiromori, Y., Nakanishi, T., Santos, M. M., et al. (2014) · Endocrinology · doi:10.1210/en.2014-1181 · Cited by 53 · see citing works
A switch in numb isoforms is a critical step in cortical development
Bani‐Yaghoub, M., Kubu, C. J., Cowling, R., Rochira, J. A., Nikopoulos, G. N., Bellum, S. C., & Verdi, J. M. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21072 · Cited by 53 · see citing works
A historical note on the mode of administration of vitamin A for the cure of night blindness
Wolf, G. (1978) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/31.2.290 · Cited by 53 · see citing works
Characterisation of the Fibroblast Growth Factor Dependent Transcriptome in Early Development
Branney, P., Faas, L., Steane, S. E., Pownall, M. E., & Isaacs, H. V. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004951 · Cited by 52 · see citing works
Sueoka, N., Lee, H., Walsh, G. L., Hong, W. K., & Kurie, J. M. (1999) · PubMed · Cited by 51 · see citing works
Developmental expression of PC3 gene is correlated with neuronal cell birthday
Iacopetti, P., Barsacchi, G., Tirone, F., Maffei, L., & Cremisi, F. (1994) · Mechanisms of Development · doi:10.1016/0925-4773(94)90085-x · Cited by 50 · see citing works
Differential Retinoic Acid Signaling in Tumors of Long- and Short-term Glioblastoma Survivors
Barbus, S., Tews, B., Karra, D., Hahn, M., Radlwimmer, B., Delhomme, N., Hartmann, C. J., Felsberg, J., Krex, D., Schackert, G., et al. (2011) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djr036 · Cited by 49 · see citing works
Leclerc, C., Lee, M., Webb, S., Moreau, M., & Miller, A. L. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00298-7 · Cited by 48 · see citing works
Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo
Lim, J.-W., Hummert, P. M., Mills, J. C., & Kroll, K. L. (2010) · Development · doi:10.1242/dev.059824 · Cited by 48 · see citing works
Flagged first, then by citations
Research works printed but not linked: 6
- [4]4. Hale F (1933) Pigs born without eyeballs. J Hered 24(3):105-106
- [100]100. Morrison SJ, Kimble J (2006) Asymmetric and symmetric stemcell divisions in development and cancer. Nature 441(7097): 1068-1074
- [102]102. Pardee AB (1989) G1 events and regulation of cell proliferation. Science 246(4930):603-608
- [183]183. Kosaka C, Sasaguri T, Komiyama Y, Takahashi H (2001) Alltrans retinoic acid inhibits vascular smooth muscle cell proliferation targeting multiple genes for cyclins and cyclindependent kinases. Hypertens Res 24(5):579-588
- [219]219. Shimada H, Umehara S, Monobe Y, Hachitanda Y, Nakagawa A, Goto S, Gerbing RB, Stram DO, Lukens JN, Matthay KK (2001) International neuroblastoma pathology classification for prognostic evaluation of patients with peripheral neuroblastic tumors: a report from the Children's Cancer Group. Cancer 92(9):2451-2461
- [28]28. fight against cancer. Nat Rev Cancer 1(3):181-193
Cited by
Sorted by citations
SARS‐CoV‐2 targets neurons of 3D human brain organoids
Ramani, A., Müller, L., Ostermann, P. N., Gabriel, E., Abida‐Islam, P., Müller‐Schiffmann, A., Mariappan, A., Goureau, O., Gruell, H., Walker, A., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2020106230 · Cited by 518 · see citing works
Human brain organoids assemble functionally integrated bilateral optic vesicles
Gabriel, E., Albanna, W., Pasquini, G., Ramani, A., Josipović, N., Mariappan, A., Schinzel, F., Karch, C. M. M., Bao, G., Gottardo, M., et al. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.07.010 · Cited by 180 · see citing works
Fatty Acid Signaling Mechanisms in Neural Cells: Fatty Acid Receptors
Falomir‐Lockhart, L. J., Cavazzutti, G. F., Giménez, E., & Toscani, A. M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00162 · Cited by 162 · see citing works
Mechanistic aspects of carotenoid health benefits – where are we now?
Bohn, T., Bonet, M. L., Borel, P., Keijer, J., Landrier, J., Milisav, I., Ribot, J., Riso, P., Winklhofer-Roob, B., Sharoni, Y., et al. (2021) · Nutrition Research Reviews · doi:10.1017/s0954422421000147 · Cited by 151 · see citing works
Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine
Ferreira, R., Napoli, J., Enver, T., Bernardino, L., & Ferreira, L. (2020) · Nature Communications · doi:10.1038/s41467-020-18042-2 · Cited by 138 · see citing works
Zhao, H. N., Thomas, S. P., Zylka, M. J., Dorrestein, P. C., & Hu, W. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c05026 · Cited by 128 · see citing works
The Role of Vitamins in Neurodegenerative Disease: An Update
Nand, S., Singh, P., Steinbusch, H. W. M., Vamanu, E., Ashraf, G. M., & Singh, M. P. (2021) · Biomedicines · doi:10.3390/biomedicines9101284 · Cited by 126 · see citing works
He, Q., Wu, Z., Li, L., Sun, W., Wang, G., Jiang, R., Hu, L., Shi, L., He, R., Wang, Y., et al. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202103878 · Cited by 113 · see citing works
Barák, M., Fedorová, V., Pospíšilová, V., Raška, J., Vochyánová, S., Sedmík, J., Hříbková, H., Klímová, H., Váňová, T., & Bohačiaková, D. (2022) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10254-3 · Cited by 100 · see citing works
Differentiation of Mesenchymal Stem Cells to Neuroglia: in the Context of Cell Signalling
George, S., Hamblin, M. R., & Abrahamse, H. (2019) · Stem Cell Reviews and Reports · doi:10.1007/s12015-019-09917-z · Cited by 97 · see citing works
Cerium oxide nanoparticles inhibit differentiation of neural stem cells
Gliga, A. R., Edoff, K., Caputo, F., Källman, T., Blom, H., Karlsson, H. L., Ghibelli, L., Traversa, E., Ceccatelli, S., & Fadeel, B. (2017) · Scientific Reports · doi:10.1038/s41598-017-09430-8 · Cited by 84 · see citing works
MEIS transcription factors in development and disease
Schulte, D., & Geerts, D. (2019) · Development · doi:10.1242/dev.174706 · Cited by 77 · see citing works
Zhao, X., Li, D., Huang, D., Song, H., Mei, H., Fang, E., Wang, X., Yang, F., Zheng, L., Huang, K., et al. (2017) · Molecular Therapy · doi:10.1016/j.ymthe.2017.12.017 · Cited by 73 · see citing works
RetractedNeurogenesis, neuronal migration, and axon guidance
Accogli, A., Addour-Boudrahem, N., & Srour, M. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64150-2.00004-6 · Cited by 72 · see citing works
Retinoic acid rewires the adrenergic core regulatory circuitry of childhood neuroblastoma
Zimmerman, M. W., Durbin, A. D., He, S., Oppel, F., Shi, H., Tao, T., Li, Z., Berezovskaya, A., Liu, Y., Zhang, J., et al. (2021) · Science Advances · doi:10.1126/sciadv.abe0834 · Cited by 69 · see citing works
Organs to Cells and Cells to Organoids: The Evolution of in vitro Central Nervous System Modelling
Pacitti, D., Privolizzi, R., & Bax, B. E. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00129 · Cited by 64 · see citing works
Therapy resistance in neuroblastoma: Mechanisms and reversal strategies
Zhou, X., Wang, X., Li, N., Guo, Y. A., Yang, X., & Lei, Y. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1114295 · Cited by 56 · see citing works
Retinoic acid induces human gastruloids with posterior embryo-like structures
Hamazaki, N., Yang, W., Kubo, C. A., Qiu, C., Martin, B., Garge, R. K., Regalado, S. G., Nichols, E. K., Pendyala, S., Bradley, N., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01487-8 · Cited by 55 · see citing works
Velte, E. K., Niedenberger, B. A., Serra, N. D., Singh, A., la Cruz, L. R.-D., Hermann, B. P., & Geyer, C. B. (2019) · Development · doi:10.1242/dev.173088 · Cited by 55 · see citing works
Tschuck, J., Nair, V. P., Galhoz, A., Zaratiegui, C., Tai, H.-M., Ciceri, G., Rothenaigner, I., Tchieu, J. H., Stockwell, B. R., Studer, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51996-1 · Cited by 54 · see citing works
Todd, L. J., Suarez, L., Quinn, C. H., & Fischer, A. J. (2017) · Stem Cells · doi:10.1002/stem.2742 · Cited by 54 · see citing works
Bioactive Lipid Signaling in Cardiovascular Disease, Development, and Regeneration
Wasserman, A. H., Venkatesan, M., & Aguirre, A. (2020) · Cells · doi:10.3390/cells9061391 · Cited by 50 · see citing works
DNA Double-Strand Breaks as Pathogenic Lesions in Neurological Disorders
Provasek, V. E., Mitra, J., Malojirao, V. H., & Hegde, M. L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094653 · Cited by 51 · see citing works
Okayasu, I., Hana, K., Nemoto, N., Yoshida, T., Saegusa, M., Yokota-Nakatsuma, A., Song, S., & Iwata, M. (2016) · BioMed Research International · doi:10.1155/2016/4874809 · Cited by 49 · see citing works
Reduce, reuse, recycle – Developmental signals in spinal cord regeneration
Cardozo, M. J., Mysiak, K. S., Becker, T., & Becker, C. G. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.05.011 · Cited by 49 · see citing works
The ancestral retinoic acid receptor was a low-affinity sensor triggering neuronal differentiation
Handberg-Thorsager, M., Gutierrez-Mazariegos, J., Arold, S. T., Nadendla, E. K., Bertucci, P. Y., Germain, P., Tomančák, P., Pierzchalski, K., Jones, J. W., Albalat, R., et al. (2018) · Science Advances · doi:10.1126/sciadv.aao1261 · Cited by 49 · see citing works
Research Progress in Vitamin A and Autism Spectrum Disorder
Liu, Z., Wang, J., Xu, Q., Hong, Q., Zhu, J., & Chi, X. (2021) · Behavioural Neurology · doi:10.1155/2021/5417497 · Cited by 49 · see citing works
Retinoic acid and depressive disorders: Evidence and possible neurobiological mechanisms
Hu, P., van Dam, A., Wang, Y., Lucassen, P. J., & Zhou, J.-N. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.013 · Cited by 47 · see citing works
Mezquita, B., & Mezquita, C. (2019) · Biomolecules · doi:10.3390/biom9100567 · Cited by 45 · see citing works
Wu, H., Zhao, J., Fu, B., Yin, S., Song, C., Zhang, J., Zhao, S., & Zhang, Y. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.336 · Cited by 44 · see citing works
Roles of vitamins in stem cells
Godoy-Parejo, C., Deng, C., Zhang, Y., Liu, W., & Chen, G. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03352-6 · Cited by 44 · see citing works
Nanoencapsulation approaches for oral delivery of vitamin A
Resende, D., Lima, S. A. C., & Reis, S. (2020) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2020.111121 · Cited by 44 · see citing works
Tian, S., Li, Y., Xu, J., Zhang, L., Zhang, J., Lu, J., Xu, X., Luan, X., Zhao, J., & Zhang, W. (2023) · Briefings in Bioinformatics · doi:10.1093/bib/bbad346 · Cited by 43 · see citing works
Hu, P., Wang, Y., Liu, J., Meng, F., Qi, X., Chen, L., van Dam, A., Joëls, M., Lucassen, P. J., & Zhou, J. (2016) · Hippocampus · doi:10.1002/hipo.22574 · Cited by 39 · see citing works
Hummel, R., Ulbrich, S., Appel, D., Li, S., Hirnet, T., Zander, S., Bobkiewicz, W., Gölz, C., & Schäfer, M. K. E. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15259 · Cited by 38 · see citing works
Transcriptional profiling of mESC-derived tendon and fibrocartilage cell fate switch
Kaji, D. A., Montero, A. M., Patel, R. S., & Huang, A. H. (2021) · Nature Communications · doi:10.1038/s41467-021-24535-5 · Cited by 39 · see citing works
D’Aloia, A., Pastori, V., Blasa, S., Campioni, G., Peri, F., Sacco, E., Ceriani, M., Lecchi, M., & Costa, B. (2024) · Cell Death Discovery · doi:10.1038/s41420-023-01790-7 · Cited by 36 · see citing works
Valdivia, L. E., Lamb, D. B., Horner, W., Wierzbicki, C., Tafessu, A., Williams, A. M., Gestri, G., Krasnow, A. M., Vleeshouwer-Neumann, T., Givens, M., et al. (2016) · Development · doi:10.1242/dev.130922 · Cited by 36 · see citing works
Zhao, Z., Shelton, S. D., Oviedo, A., Baker, A. L., Bryant, C. P., Omidvarnia, S., & Du, L. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-1531-2 · Cited by 35 · see citing works
Rudolf, M. A., Andreeva, A. Y., Kozlowski, M. M., Kim, C. E., Moskowitz, B. A., Anaya, A., Kelley, M. W., & Corwin, J. T. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0306-20.2020 · Cited by 35 · see citing works
Cooper, F., Gentsch, G. E., Mitter, R., Bouissou, C., Healy, L. E., Hernandez-Rodriguez, A. R., Smith, J. C., & Bernardo, A. S. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.02.018 · Cited by 34 · see citing works
Vitamin A and inflammatory bowel diseases: from cellular studies and animal models to human disease
Barbalho, S. M., Goulart, R. D. Á., & Batista, G. L. D. S. A. (2018) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2019.1543588 · Cited by 33 · see citing works
Impact of Cancer Stem Cells on Therapy Resistance in Gastric Cancer
Otaegi-Ugartemendia, M., Matheu, A., & Carrasco‐García, E. (2022) · Cancers · doi:10.3390/cancers14061457 · Cited by 32 · see citing works
Zieger, E., & Schubert, M. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.09.001 · Cited by 31 · see citing works
Hong, S., Ngo, H.-P.-T., Nam, H.-K., Kim, K.-R., Kang, L., & Oh, D. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.00848-16 · Cited by 31 · see citing works
Peptide Regulation of Cell Differentiation
Khavinson, V. K., Linkova, N. S., Diatlova, A., & Trofimova, S. (2019) · Stem Cell Reviews and Reports · doi:10.1007/s12015-019-09938-8 · Cited by 30 · see citing works
Sachana, M., Willett, C., Pistollato, F., & Bal‐Price, A. (2021) · Reproductive Toxicology · doi:10.1016/j.reprotox.2021.06.006 · Cited by 31 · see citing works
Sánchez‐Hernández, D., Anderson, G. H., Poon, A. N., Pannia, E., Cho, C. E., Huot, P. S. P., & Kubant, R. (2016) · Nutrition Research · doi:10.1016/j.nutres.2016.09.009 · Cited by 30 · see citing works
Nierode, G. J., Gopal, S., Kwon, P. S., Clark, D. S., Schaffer, D. V., & Dordick, J. S. (2018) · Biotechnology and Bioengineering · doi:10.1002/bit.26839 · Cited by 29 · see citing works
Lin, Y., Lin, Y.-W., Nhieu, J., Zhang, X., & Wei, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114125 · Cited by 29 · see citing works
Protocol for mouse adult neural stem cell isolation and culture
Ahmed, A. K. M. A., Isaksen, T. J., & Yamashita, T. (2021) · STAR Protocols · doi:10.1016/j.xpro.2021.100522 · Cited by 29 · see citing works
Differentiation enhances Zika virus infection of neuronal brain cells
Martín, C. S.-S., Li, T. Y., Bouquet, J., Streithorst, J. A., Yu, G., Paranjpe, A., & Chiu, C. Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-32400-7 · Cited by 29 · see citing works
Impacts of vitamin A deficiency on biological rhythms: Insights from the literature
Guo, X., Wang, H., Xu, J., & Hua, H. M. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.886244 · Cited by 28 · see citing works
Neurogenic and Neuroprotective Potential of Stem/Stromal Cells Derived from Adipose Tissue
Figiel‐Dabrowska, A., Radoszkiewicz, K., Rybkowska, P., Krześniak, N. E., Sulejczak, D., & Sarnowska, A. (2021) · Cells · doi:10.3390/cells10061475 · Cited by 28 · see citing works
On the role of retinoic acid in virus induced inflammatory response in cornea
Jaggi, U., Varanasi, S. K., Bhela, S., & Rouse, B. T. (2018) · Microbes and Infection · doi:10.1016/j.micinf.2018.04.007 · Cited by 28 · see citing works
Shokrollahi, E., Nourazarian, A., Rahbarghazi, R., Salimi, L., Karbasforush, S., Khaksar, M., Salarinasab, S., Abhari, A., & Heidarzadeh, M. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28704 · Cited by 28 · see citing works
Age-Related Expression of a Repeat-Rich Intergenic Long Noncoding RNA in the Rat Brain
Kour, S., & Rath, P. C. (2016) · Molecular Neurobiology · doi:10.1007/s12035-015-9634-z · Cited by 27 · see citing works
A Single-Cell Transcriptomic Analysis of the Mouse Hippocampus After Voluntary Exercise
Methi, A., Islam, R., Kaurani, L., Sakib, M. S., Krüger, D. M., Peña, T., Burkhardt, S., Liebetanz, D., & Fischer, A. (2024) · Molecular Neurobiology · doi:10.1007/s12035-023-03869-9 · Cited by 30 · see citing works
Liu, Q., Bortle, K. V., Zhang, Y., Zhao, M., Zhang, J. Z., Geller, B. S., Gruber, J. J., Jiang, C., Wu, J. C., & Snyder, M. P. (2018) · Scientific Reports · doi:10.1038/s41598-018-31192-0 · Cited by 27 · see citing works
Retinoic acid signaling drives differentiation toward the absorptive lineage in colorectal cancer
Wester, R. A., van Voorthuijsen, L., Neikes, H. K., Dijkstra, J. J., Lamers, L. A., Frölich, S., van der Sande, M., Logie, C., Lindeboom, R. G. H., & Vermeulen, M. (2021) · iScience · doi:10.1016/j.isci.2021.103444 · Cited by 26 · see citing works
Tissue-Engineered Models of the Human Brain: State-of-the-Art Analysis and Challenges
Tarricone, G., Carmagnola, I., & Chiono, V. (2022) · Journal of Functional Biomaterials · doi:10.3390/jfb13030146 · Cited by 28 · see citing works
Mungenast, L., Nieminen, R., Gaiser, C., Faia-Torres, A. B., Rühe, J., & Suter‐Dick, L. (2023) · Biomaterials and Biosystems · doi:10.1016/j.bbiosy.2023.100081 · Cited by 26 · see citing works
Zhu, K., Xia, Y.-R., Tian, X., He, Y.-C., Zhou, J., Han, R., Guo, H., Song, T., Chen, L., & Tian, X.-D. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1271381 · Cited by 17 · see citing works
Kang, J.-B., Park, D.-J., Shah, M.-A., & Koh, P. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135979 · Cited by 25 · see citing works
Nyffeler, J., Willis, C. M., Harris, F. R., Word, L. J., Judson, R., Everett, L. J., & Harrill, J. (2022) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2022.116032 · Cited by 25 · see citing works
Synergy of Nanotopography and Electrical Conductivity of PEDOT/PSS for Enhanced Neuronal Development
Bianchi, M., Guzzo, S., Lunghi, A., Greco, P., Pisciotta, A., Murgia, M., Carnevale, G., Fadiga, L., & Biscarini, F. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c15278 · Cited by 25 · see citing works
Tang, B. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.10.008 · Cited by 26 · see citing works
dos Santos, M. G., Gomes, J. R., & Costa, M. D. M. (2023) · Cell Biology International · doi:10.1002/cbin.12093 · Cited by 23 · see citing works
Santos, A. K., Gomes, K. N., Parreira, R. C., Scalzo, S., Pinto, M. C. X., Santiago, H. C., Birbrair, A., Sack, U., Ulrich, H., & Resende, R. R. (2021) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10218-7 · Cited by 23 · see citing works
Lim, J., Choi, H., & Choi, H. J. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13085 · Cited by 23 · see citing works
Oh, H., Yoo, D., Park, S., Lee, S., & Kim, W. (2022) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2022.113891 · Cited by 22 · see citing works
P2X7 receptor isoform B is a key drug resistance mediator for neuroblastoma
Arnaud-Sampaio, V. F., Bento, C. A., Glaser, T., Adinolfi, E., Ulrich, H., & Lameu, C. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.966404 · Cited by 22 · see citing works
Frazel, P. W., Labib, D., Fisher, T., Brosh, R., Pirjanian, N., Marchildon, A. E., Boeke, J. D., Fossati, V., & Liddelow, S. A. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01424-2 · Cited by 24 · see citing works
Koch, K., Schlüppmann, K., Hüsken, S., Stark, L. M., Förster, N., Masjosthusmann, S., Klose, J., Dönmez, A., & Fritsche, E. (2025) · Environment International · doi:10.1016/j.envint.2025.109400 · Cited by 21 · see citing works
Esrrb is a cell-cycle-dependent associated factor balancing pluripotency and XEN differentiation
Levy, S. H., Cohen, S. F., Arnon, L., Lahav, S., Awawdy, M., Alajem, A., Bavli, D., Sun, X., Buganim, Y., & Ram, O. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.04.016 · Cited by 17 · see citing works
A CYPome-wide study reveals new potential players in the pathogenesis of Parkinson’s disease
Hartz, P., Fehlmann, T., Wagenpfeil, G., Unger, M. M., & Bernhardt, R. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1094265 · Cited by 21 · see citing works
Zieger, E., Candiani, S., Garbarino, G., Croce, J. C., & Schubert, M. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0727-8 · Cited by 21 · see citing works
Girardi, C. S., Rostirolla, D. C., Lini, F. J. M., Brum, P. O., Delgado, J., Ribeiro, C. T., Teixeira, A. A., Peixoto, D. O., Heimfarth, L., Kunzler, A., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.11.014 · Cited by 21 · see citing works
NSC ‐34 motor neuron‐like cells are sensitized to ferroptosis upon differentiation
Martinez, A. M., Mirkovic, J., Stanisz, Z., Patwari, F. S., & Yang, W. S. (2018) · FEBS Open Bio · doi:10.1002/2211-5463.12577 · Cited by 21 · see citing works
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos
Lichtig, H., Artamonov, A., Polevoy, H., Reid, C. D., Bielas, S. L., & Frank, D. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00075 · Cited by 21 · see citing works
Development of differentiation modulators and targeted agents for treating neuroblastoma
Jin, Z., Lu, Y., Wu, Y., Che, J., & Dong, X. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112818 · Cited by 21 · see citing works
Ribeiro, R., Nicoli, J. R., Santos, G., & dos Santos, J. L. (2019) · Nutritional Neuroscience · doi:10.1080/1028415x.2019.1660485 · Cited by 26 · see citing works
Gomez, R. L., Woods, L. M., Ramachandran, R., Tayoun, A. N. A., Philpott, A., & Ali, F. R. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.943924 · Cited by 20 · see citing works
RNA Polymerase II transcription independent of TBP in murine embryonic stem cells
Kwan, J. Z. J., Nguyen, T. F., Uzozie, A. C., Budzyński, M. A., Cui, J. H., Lee, J. M., Petegem, F. V., Lange, P. F., & Teves, S. S. (2023) · eLife · doi:10.7554/elife.83810 · Cited by 19 · see citing works
Establishing and maintaining Hox profiles during spinal cord development
Miller, A., & Dasen, J. S. (2023) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2023.03.014 · Cited by 20 · see citing works
Generation of iPSC-derived human forebrain organoids assembling bilateral eye primordia
Gabriel, E., Albanna, W., Pasquini, G., Ramani, A., Josipović, N., Mariappan, A., Riparbelli, M. G., Callaini, G., Karch, C. M. M., Goureau, O., et al. (2023) · Nature Protocols · doi:10.1038/s41596-023-00814-x · Cited by 20 · see citing works
Moescheid, M. F., Lu, Z., Soria, C. L. D., Quack, T., Puckelwaldt, O., Holroyd, N. E., Holzaepfel, P., Haeberlein, S., Rinaldi, G., Berriman, M., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1228 · Cited by 19 · see citing works
Kang, J.-B., Son, H.-K., Shah, M.-A., & Koh, P. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300072 · Cited by 19 · see citing works
Park, E., Tjia, M., Zuo, Y., & Chen, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3028-17.2018 · Cited by 18 · see citing works
An optimized method for neuronal differentiation of embryonic stem cells in vitro
Li, Y., Mao, X., Xianyi, Z., Su, Y.-T., Zhou, X., Shi, K., & Zhao, S. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108486 · Cited by 18 · see citing works
Draut, H., Liebenstein, T., & Begemann, G. (2019) · Biomolecules · doi:10.3390/biom9120860 · Cited by 19 · see citing works
Unsicker, C., Cristian, F.-B., von Hahn, M., Eckstein, V., Rappold, G., & Berkel, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-81241-4 · Cited by 20 · see citing works
Aligned contiguous microfiber platform enhances neural differentiation of embryonic stem cells
Liu, Z., & Hu, Z. (2018) · Scientific Reports · doi:10.1038/s41598-018-24522-9 · Cited by 19 · see citing works
Role of miR-124 in the regulation of retinoic acid-induced Neuro-2A cell differentiation
You, Q., Dong, S., Han, Y., Pi, R., Du, Y.-J., & Dong, S.-Z. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.270417 · Cited by 18 · see citing works
Effects of all-trans and 9-cis retinoic acid on differentiating human neural stem cells in vitro
Kubíčková, B., Martinkova, S., Bohačiaková, D., Nezvedová, M., Liu, R., Brózman, O., Spáčil, Z., & Hilscherová, K. (2023) · Toxicology · doi:10.1016/j.tox.2023.153461 · Cited by 18 · see citing works
Kour, S., & Rath, P. C. (2015) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0671-x · Cited by 18 · see citing works
Zieger, E., Garbarino, G., Robert, N. S. M., Yu, J., Croce, J. C., Candiani, S., & Schubert, M. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2734-3 · Cited by 17 · see citing works
Masoumi, N., Ghollasi, M., Halabian, R., Eftekhari, E., & Ghiasi, M. (2023) · Regenerative Therapy · doi:10.1016/j.reth.2023.04.001 · Cited by 17 · see citing works
Camdzic, M., Aga, D. S., & Atilla‐Gokcumen, G. E. (2023) · Environment & Health · doi:10.1021/envhealth.3c00022 · Cited by 16 · see citing works
Yu, L., Yong, Y., Zhang, B., Bai, X., Fei, Q., & Zhang, L. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29788 · Cited by 17 · see citing works
- Authors
- Janesick, A., Wu, S. C., & Blumberg, B.
- Affiliations
- University of California, Irvine (US)
- Corresponding author
- Blumberg, Bruce
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2015-01-06
- Volume
- 72
- Issue
- 8
- Pages
- 1559-1576
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11113123
- OpenAlex
- W2117145998
- Cited by
- 295
- References
- 268
- Citations by year
- 2026: 15 · 2025: 37 · 2024: 30 · 2023: 36 · 2022: 25 · 2021: 44 · 2020: 31 · 2019: 24 · 2018: 22 · 2017: 16 · 2016: 13 · 2015: 2
- FWCI
- 2.22
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by-nc-nd)
- Funders
- National Science Foundation
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- retinoic acid signaling, neuronal differentiation, primary neurogenesis, retinoic acid receptor, proneural transcription factors, vitamin A deficiency, dedifferentiation, tumor differentiation
- MeSH terms
- Animals, Antigens, Neoplasm, Antineoplastic Agents, Humans, Neoplasms, Neurons, Tretinoin, Signal Transduction, Receptors, Retinoic Acid, Cell Cycle Proteins, Neurogenesis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review