Cited by 292Neurogenesis and neuroplasticity mechanismsDevelopmental Biology and Gene RegulationRetinal Development and Disorders

The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.

Math1-driven GFP expression in the developing nervous system of transgenic mice

Lumpkin, Ellen A., Collisson, Tandi, Parab, Preeti, Omer-Abdalla, Adil, Haeberle, Henry, Chen, Ping, Doetzlhofer, Angelika, White, Patricia, Groves, Andrew, Segil, Neil, Johnson, Jane E.·2003·Gene Expression Patterns

DOI 10.1016/s1567-133x(03)00089-9

Open this paper in CoChat — free account

Abstract

Math1 is a bHLH transcription factor expressed in neural progenitor cells in multiple regions of the nervous system. Previously we identified a Math1 enhancer that directs expression of reporter genes in a Math1 specific pattern [Development 127 (2000) 1185]. We have used a portion of this enhancer to drive expression of a nuclear GFP reporter in the Math1 lineage in transgenic mice. In this transgenic mouse strain, GFP is expressed in Math1 domains in the (1). developing spinal cord in progenitors to dI1 dorsal interneurons, (2). granule-cell progenitors in the developing cerebellum, (3). Merkel cells in the skin, and (4). hair cells in the developing vestibular and auditory systems. Furthermore, non-Math1 related expression is detected that is likely due to the absence of inhibitory regulatory sequences from the transgene. These expression domains include (1). the apical ectodermal ridge in developing limbs, (2). post-mitotic cells in the developing cortex and spinal cord, (3). the dentate gyrus, (4). retina, and (5). olfactory epithelium. Because GFP marks specific neuronal cell types in living tissue, this transgenic strain is a powerful tool for future studies on the development and electrophysiological properties of distinct cell types in the central nervous system and in sensory systems.

Integrity signals

Registry

Crossref · 10.1016/s1567-133x(03)00089-9

Cites

30 of 30 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

NeuN, a neuronal specific nuclear protein in vertebratesxs
Mullen, R. J., Buck, C. R., & Smith, A. M. (1992) · Development · doi:10.1242/dev.116.1.201 · Cited by 2,351
Math1 : An Essential Gene for the Generation of Inner Ear Hair Cells
Bermingham, N. A., Hassan, B. A., Price, S. D., Vollrath, M. A., Ben‐Arie, N., Eatock, R. A., Bellen, H. J., Lysakowski, A., & Zoghbi, H. Y. (1999) · Science · doi:10.1126/science.284.5421.1837 · Cited by 1,093
Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm
Liem, K. F., Tremml, G., Roelink, H., & Jessell, T. M. (1995) · Cell · doi:10.1016/0092-8674(95)90276-7 · Cited by 1,071
The structure and function of a slowly adapting touch corpuscle in hairy skin
Iggo, A., & Muir, A. R. (1969) · Journal of Physiology · doi:10.1113/jphysiol.1969.sp008721 · Cited by 749
Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons
Dodd, J., Brenner‐Morton, S., Karagogeos, D., Yamamoto, M., & Jessell, T. M. (1988) · Neuron · doi:10.1016/0896-6273(88)90194-8 · Cited by 741
Math1 is essential for genesis of cerebellar granule neurons
Ben‐Arie, N., Bellen, H. J., Armstrong, D. L., McCall, A. E., Gordadze, P. R., Guo, Q., Matzuk, M. M., & Zoghbi, H. Y. (1997) · Nature · doi:10.1038/36579 · Cited by 702
The axonal glycoprotein TAG-1 is an immunoglobulin superfamily member with neurite outgrowth-promoting activity
Furley, A. J., Brenner‐Morton, S., Manalo, D. J., Karagogeos, D., Dodd, J., & Jessell, T. M. (1990) · Cell · doi:10.1016/0092-8674(90)90223-2 · Cited by 564
The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination
Chen, P., Johnson, J. E. B., Zoghbi, H. Y., & Segil, N. (2002) · Development · doi:10.1242/dev.129.10.2495 · Cited by 528
Self-citation
Genetic regulation of cerebellar development
Wang, V. Y., & Zoghbi, H. Y. (2001) · Nature reviews. Neuroscience · doi:10.1038/35081558 · Cited by 490
Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells.Preprint
Lo, L., Johnson, J. E. B., Wuenschell, C. W., Saito, T., & Anderson, D. J. (1991) · Genes & Development · doi:10.1101/gad.5.9.1524 · Cited by 435
Self-citation

Show all 30 references

Research works printed but not linked: 1

Lim, 1985, Developmental morphology of the mouse inner ear, Acta Otolaryngol., 422, 1

Sorted by citations

Items 201–292 of 292

Neuropilin2 regulates the guidance of post-crossing spinal commissural axons in a subtype-specific manner
Tran, T. S., Carlin, E., Lin, R., Martinez, E. A., Johnson, J. E. B., & Kaprielian, Z. (2013) · Neural Development · doi:10.1186/1749-8104-8-15 · Cited by 16
Self-citation
Endogenous cerebellar neurogenesis in adult mice with progressive ataxia
Kumar, M., Csaba, Z., Peineau, S., Srivastava, R., Rasika, S., Mani, S., Gressèns, P., & Ghouzzi, V. E. (2014) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.137 · Cited by 16
Gene therapy: an emerging therapy for hair cells regeneration in the cochlea
Wang, J., Zheng, J., Wang, H., He, H., Li, S., Zhang, Y., Wang, Y., Xu, X., & Wang, S. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1177791 · Cited by 14
Efficient induction of inner ear hair cell-like cells from mouse ES cells using combination of Math1 transfection and conditioned medium from ST2 stromal cells
Ouji, Y., Sakagami, M., Omori, H., Higashiyama, S., Kawai, N., Kitahara, T., Wanaka, A., & Yoshikawa, M. (2017) · Stem Cell Research · doi:10.1016/j.scr.2017.06.013 · Cited by 14
The Purinergic Receptor P2rx3 is Required for Spiral Ganglion Neuron Branch Refinement during Development
Wang, Z., Jung, J. S., Inbar, T. C., Rangoussis, K. M., Faaborg-Andersen, C. C., & Coate, T. M. (2020) · eNeuro · doi:10.1523/eneuro.0179-20.2020 · Cited by 15
Temporal-specific roles of Fragile X mental retardation protein in the development of hindbrain auditory circuit
Wang, X., Kohl, A., Yu, X., Zorio, D. A. R., Klar, A., Sela‐Donenfeld, D., & Wang, Y. (2020) · Development · doi:10.1242/dev.188797 · Cited by 13
Skin relaxation predicts neural firing rate adaptation in SAI touch receptors
Williams, A. L., Gerling, G. J., Wellnitz, S. A., et al. (2010) · Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society · doi:10.1109/iembs.2010.5626264 · Cited by 14
Self-citation
Usher syndrome IIIA: a review of the disorder and preclinical research advances in therapeutic approaches
Marouf, A., Johnson, B. R. G., & Alagramam, K. N. (2022) · Human Genetics · doi:10.1007/s00439-022-02446-9 · Cited by 13
Experimental drugs for the prevention or treatment of sensorineural hearing loss
Kempfle, J. S., & Jung, D. H. (2023) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2023.2242253 · Cited by 13
HIC1 Represses Atoh1 Transcription and Hair Cell Differentiation in the Cochlea
Abdul‐Aziz, D., Hathiramani, N. R., Phung, L., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.02.022 · Cited by 13
Cellular Targeting for Cochlear Gene Therapy
Ryan, A. F., Mullen, L., & Doherty, J. K. (2009) · Advances in oto-rhino-laryngology · doi:10.1159/000218210 · Cited by 12
The Repression of Atoh1 by Neurogenin1 during Inner Ear Development
Gálvez, H., Tena, J. J., Giráldez, F., & Abelló, G. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00321 · Cited by 12
Epigenetic regulation and signalling pathways in Merkel cell development
Oss-Ronen, L., & Cohen, I. (2021) · Experimental Dermatology · doi:10.1111/exd.14415 · Cited by 14
The expression profile of the tumor suppressor gene Lzts1 suggests a role in neuronal development
Kropp, M., & Wilson, S. I. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23777 · Cited by 14
Trimodal single-cell profiling of transcriptome, epigenome, and 3D genome in complex tissues with scHiCAR
Wei, X., Xu, Y.-Y., Yang, D.-C., Kim, K., Yi, L., Luo, W.-Z., Lin, X., Xiang, Y., Williams, A. B., Wang, X.-T., et al. (2026) · Nature Biotechnology · doi:10.1038/s41587-026-03013-7 · Cited by 16
Thérapie cellulaire dans l’oreille interne
El-Amraoui, A., & Petit, C. (2010) · médecine/sciences · doi:10.1051/medsci/20102611981 · Cited by 11
Evolution of the functionally conserved DCC gene in birds
Patthey, C., Tong, Y. G., Tait, C. M., & Wilson, S. I. (2017) · Scientific Reports · doi:10.1038/srep42029 · Cited by 12
Murine cochlear damage models in the context of hair cell regeneration research
Maraslioglu-Sperber, A., Blanc, F., & Heller, S. (2024) · Hearing Research · doi:10.1016/j.heares.2024.109021 · Cited by 10
SoxC transcription factors shape the epigenetic landscape to establish competence for sensory differentiation in the mammalian organ of Corti
Wang, X., Llamas, J., Trecek, T., Shi, T., Tao, L., Makmura, W., Crump, J. G., Segil, N., & Gnedeva, K. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2301301120 · Cited by 10
Self-citation
Transgenic models for investigating the nervous system: Currently available neurofluorescent reporters and potential neuronal markers
Yamakawa, M., Santosa, S. M., Chawla, N., Ivakhnitskaia, E., Pino, M. D., Giakas, S., Nadel, A., Bontu, S., Tambe, A., Guo, K., et al. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129595 · Cited by 13
Generation of Atoh1-rtTA transgenic mice: a tool for inducible gene expression in hair cells of the inner ear
Cox, B. C., Dearman, J., Brancheck, J., et al. (2014) · Scientific Reports · doi:10.1038/srep06885 · Cited by 10
Statistical analysis and modeling of variance in the SA-I mechanoreceptor response to sustained indentation
Lesniak, D. R., Wellnitz, S. A., Gerling, G. J., & Lumpkin, E. A. (2009) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/iembs.2009.5334487 · Cited by 10
Self-citation
Merkel cells and keratinocytes in oral mucosa are activated by mechanical stimulation
Tong, C., Moayedi, Y., & Lumpkin, E. A. (2024) · Physiological Reports · doi:10.14814/phy2.15826 · Cited by 9
Self-citation
Mapping the developmental potential of mouse inner ear organoids at single-cell resolution
Waldhaus, J., Jiang, L., Liu, L., Liu, J., & Duncan, R. K. (2024) · iScience · doi:10.1016/j.isci.2024.109069 · Cited by 9
GATA3 maintains the quiescent state of cochlear supporting cells by regulating p27kip1
Xu, J., Yu, D., Dong, X., Xie, X., Xu, M., Guo, L., Huang, L., Tang, Q., & Gan, L. (2021) · Scientific Reports · doi:10.1038/s41598-021-95427-3 · Cited by 9
Electroporation of the Hindbrain to Trace Axonal Trajectories and Synaptic Targets in the Chick Embryo
Kohl, A., Hadas, Y., Klar, A., & Sela‐Donenfeld, D. (2013) · Journal of Visualized Experiments · doi:10.3791/50136 · Cited by 9
Regenerative Therapy Approaches and Encountered Problems in Sensorineural Hearing Loss
Kelleci, K., & Gölebatmaz, E. (2022) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x17666220429121714 · Cited by 8
The regulation of gene expression in hair cells
Ryan, A. F., Ikeda, R., & Masuda, M. (2015) · Hearing Research · doi:10.1016/j.heares.2014.12.013 · Cited by 8
Stem cell differentiation with consistent lineage commitment induced by a flash of ultrafast-laser activation in vitro and in vivo
Tang, W., Wang, H., Zhao, X., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110486 · Cited by 8
A Novel in vitro Model Delineating Hair Cell Regeneration and Neural Reinnervation in Adult Mouse Cochlea
Li, W., Quan, Y., Huang, M., Wei, W., Shu, Y., Li, H., & Chen, Z. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.757831 · Cited by 7
CDK2 regulates aminoglycoside-induced hair cell death through modulating c-Jun activity: Inhibiting CDK2 to preserve hearing
Tao, L., & Segil, N. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1013383 · Cited by 7
Self-citation
Annexin A4 Is Dispensable for Hair Cell Development and Function
Li, N., Xi, Y., Du, H., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.680155 · Cited by 7
Deletion of Btg1 Induces Prmt1-Dependent Apoptosis and Increased Stemness in Shh-Type Medulloblastoma Cells Without Affecting Tumor Frequency
Ceccarelli, M., D’Andrea, G., Micheli, L., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00226 · Cited by 7
Leaving the midline
Reeber, S. L., & Kaprielian, Z. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.3.9156 · Cited by 7
Atoh1 mediated disturbance of neuronal maturation by perinatal hypoxia induces cognitive deficits
Cai, X., Ma, S.-Y., Tang, M.-H., Hu, L., Wu, K., Zhang, Z., Zhang, Y., Lin, Y., Patel, N. D., Yang, Z.-C., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06846-7 · Cited by 6
Therapeutic radiation drives leptomeningeal dissemination of medulloblastoma through an innate immune process
Nör, C., Kharas, K., Rasnitsyn, A., Vladoiu, M. C., Cho, N. W., Young, J. S., Nör, F., Mankahla, N., Haapasalo, J. A., Nordfors, K., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.06.016 · Cited by 7
Lipidome signatures of metastasis in a transgenic mouse model of sonic hedgehog medulloblastoma
Huang, D., Liu, J., Eldridge, R. C., et al. (2020) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-020-02837-9 · Cited by 6
Tactile sensitivity in the rat: a correlation between receptor structure and function
Guzun, L., Fortier-Poisson, P., Langlais, J.-S., & Smith, A. M. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06193-7 · Cited by 6
Excess cerebellar granule neurons induced by the absence of p75NTR during development elicit social behavior deficits in mice
Zanin, J. P., Pandya, M. A., Espinoza, D., Friedman, W., & Shiflett, M. W. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1147597 · Cited by 6
Strategies to investigate gene expression and function in granule cells
Savill, R. M., Scotting, P. J., & Coyle, B. (2005) · The Cerebellum · doi:10.1080/14734220500367790 · Cited by 6
Molecular regulatory mechanisms of Merkel cell differentiation
Cervellera, C. F., Mazziotta, C., Mazzoni, E., Bononi, I., Iaquinta, M. R., Tognon, M. G., Martini, F., & Rotondo, J. C. (2025) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.70067 · Cited by 5
Childhood cancer mutagenesis caused by transposase-derived PGBD5
Yamada, M., Keller, R. R., Gutierrez, R. L., Cameron, D., Suzuki, H., Sanghrajka, R. M., Vaynshteyn, J., Gerwin, J. N., Maura, F., Hooper, W. F., et al. (2024) · Science Advances · doi:10.1126/sciadv.adn4649 · Cited by 6
An Independent Construct for Conditional Expression of Atonal Homolog-1
Parker, M. A., Cheng, Y., Kinouchi, H., et al. (2013) · Human Gene Therapy Methods · doi:10.1089/hgtb.2013.014 · Cited by 5
Isolation of Distinct Cell Populations from the Developing Cerebellum by Microdissection
Yuelling, L. W., Du, F., Li, P., et al. (2014) · Journal of Visualized Experiments · doi:10.3791/52034 · Cited by 4
Cidea Targeting Protects Cochlear Hair Cells and Hearing Function From Drug‐ and Noise‐Induced Damage
Zhang, S., Qiang, R., Zhang, Y., et al. (2025) · Advanced Science · doi:10.1002/advs.202517206 · Cited by 3
Vertebrate spinal commissural neurons: a model system for studying axon guidance beyond the midline
Martinez, E. A., & Tran, T. S. (2015) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.173 · Cited by 3
High quality mapping of chromatin at or near the nuclear lamina from small numbers of cells reveals cell cycle and developmental changes of chromatin at the nuclear periphery
Tran, J. R., Zheng, X., Adam, S. A., Goldman, R. D., & Zheng, Y. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac762 · Cited by 4
Trauma and Sensory Systems: Biological Mechanisms Involving the Skin and the 17q21 Gene Cluster
Korgan, A. C., Prendergast, K., Rosenhauer, A. M., Morrison, K. E., Jovanović, T., & Bale, T. L. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.11.003 · Cited by 3
Establishment of mice expressing EGFP in the placode‐derived inner ear sensory cell lineage and FACS‐array analysis focused on the regional specificity of the otocyst
Fujimoto, C., Ozeki, H., Uchijima, Y., Suzukawa, K., Mitani, A., Fukuhara, S., Nishiyama, K., Kurihara, Y., Kondo, K., Aburatani, H., et al. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22468 · Cited by 3
Protocol to photoactivate adipose-derived stem cell differentiation using a tightly-focused femtosecond laser
Tang, W., Wang, H., & He, H. (2022) · STAR Protocols · doi:10.1016/j.xpro.2022.101574 · Cited by 2
A cell type–specific approach to elucidate the role of miR-96 in inner ear hair cells
Gwilliam, K., Sperber, M., Perry, K., Rose, K. P., Ginsberg, L., Paladugu, N., Song, Y., Milon, B. C., Elkon, R., & Hertzano, R. P. (2024) · Frontiers in Audiology and Otology · doi:10.3389/fauot.2024.1400576 · Cited by 2
Notch Pathway Regulation of Intestinal Cell Fate
Dempsey, P. J., Bohin, N., & Samuelson, L. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00006-2 · Cited by 3
Notch Pathway Regulation of Intestinal Cell Fate
Dussen, K. L. V., Dempsey, P. J., & Samuelson, L. C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382026-6.00011-7 · Cited by 2
Alternative LIM homeodomain splice variants are dynamically regulated at key developmental steps in vertebrates
Wheaton, B. J., Häggström, S., Muppavarapu, M., et al. (2022) · Developmental Dynamics · doi:10.1002/dvdy.466 · Cited by 2
Ezh2 Delays Activation of Differentiation Genes During Normal Cerebellar Granule Neuron Development and in MedulloblastomaPreprint
Purzner, J., Brown, A. S., Purzner, T., Ellis, L., Broski, S., Litzenburger, U. M., Andrews, K., Sharma, A., Wang, X., Taylor, M. D., et al. (2025) · eLife · doi:10.7554/elife.105339.1 · Cited by 2
The chromatin remodeler Brg1 is essential for cochlear sensory epithelium differentiation and patterning
Song, Y., Dou, Z.-L., Liu, W., Zhang, A., Gao, X., Shi, H., Zhang, Z., Gao, J., & Jin, Y. (2025) · Human Molecular Genetics · doi:10.1093/hmg/ddaf019 · Cited by 1
A Low Dose of Rapamycin Promotes Hair Cell Differentiation by Enriching SOX2+ Progenitors in the Neonatal Mouse Inner Ear Organoids
Wu, W., Chen, P., Yang, J., et al. (2024) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-024-00938-1 · Cited by 1
Self-citation
Gfi1 in the inner ear: A retrospective review
Li, Z., Chen, H., & Feng, H. (2025) · Developmental Dynamics · doi:10.1002/dvdy.70019 · Cited by 1
Childhood cancer mutagenesis caused by a domesticated DNA transposasePreprint
Keller, R. R., Yamada, M., Cameron, D., Suzuki, H., Sanghrajka, R. M., Vaynshteyn, J., Gerwin, J. N., Maura, F., Hooper, W. F., Shah, M. J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.05.498128 · Cited by 1
Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasisPreprint
Clary, R. C., Jenkins, B. A., & Lumpkin, E. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.14.528558 · Cited by 1
Self-citation
Irx3/5 define the cochlear sensory domain and regulate vestibular and cochlear sensory patterning in the mammalian inner earPreprint
Liu, Y., Qin, T., Weng, X., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.24.620152 · Cited by 1
Ezh2 Delays Activation of Differentiation Genes During Normal Cerebellar Granule Neuron Development and in MedulloblastomaPreprint
Purzner, J., Brown, A. S., Purzner, T., Ellis, L., Broski, S., Litzenburger, U. M., Andrews, K., Sharma, A., Wang, X., Taylor, M. D., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.21.624171 · Cited by 2
Social Behavior in Medulloblastoma: Functional Analysis of Tumor-Supporting Glial Cells
Zong, H. (2012) · doi:10.21236/ada566929
Investigating the Fate of Pre-neoplastic Cells in a Mouse Model of Medulloblastoma
Kessler, J. D. (2009)
Genetic basis of skin sensitivity
Mglinets, V. A. (2015) · Biology Bulletin Reviews · doi:10.1134/s2079086415040064
Enrichment of therapeutic hematopoietic stem cell populations from embryonic stem cells
Gilner, J. B. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/0swe-w763
Genetic and Environmental Factors that Control Merkel Cell Development and Survival
Logan-Graf, G. (2017) · D-Scholarship@Pitt (University of Pittsburgh)
Distinct roles of Tfap2A & Tfap2B in the diversification of GABAergic neuronal subtypes in the cerebellum
Zainolabidin, N. (2017) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/72795
Faculty Opinions recommendation of Are there multiple cells of origin of Merkel cell carcinoma?
Nghiem, P. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732451390.793542604
Activin signaling informs the graded pattern of terminal mitosis and hair cell differentiation in the mammalian cochleaPreprint
Prajapati-DiNubila, M., Benito‐Gonzalez, A., Golden, E. J., Zhang, S.-R., & Doetzlhofer, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/380055
Self-citation
A Tumor-derived Niche Cell Promotes Tumor Growth in Medulloblastoma
Ventura, P. B. (2015) · doi:10.18130/v3754q
Faculty Opinions recommendation of Applications of Lgr5-Positive Cochlear Progenitors (LCPs) to the Study of Hair Cell Differentiation.
Yamoah, E. N. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735335253.793584992
Faculty Opinions recommendation of Epidermal progenitors give rise to Merkel cells during embryonic development and adult homeostasis.
Leverkus, M. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1165130.630330
Dissecting synaptic mechanisms of sound encoding in the mouse cochlea
Jean, P. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7450
Faculty Opinions recommendation of The Repression of Atoh1 by Neurogenin1 during Inner Ear Development.
Fritzsch, B. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732080912.793538806
Faculty Opinions recommendation of Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents.
Fekete, D. M., & Munnamalai, V. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732331706.793546796
Reactivation of the progenitor gene Trim71 enhances the mitotic and hair cell-forming potential of cochlear supporting cellsPreprint
Li, X., Morgan, C., Nadar‐Ponniah, P. T., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.12.523802
Self-citation
Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasisPreprint
Clary, R. C., Jenkins, B. A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368.1
Self-citation
Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasisPreprint
Clary, R. C., Jenkins, B. A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368
Self-citation
Reviewer #2 (Public Review): Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
Clary Rachel, C., Jenkins Blair, A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368.1.sa2
Self-citation
Reviewer #1 (Public Review): Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
Clary Rachel, C., Jenkins Blair, A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368.1.sa3
Self-citation
Reviewer #4 (Public Review): Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
Clary, R. C., Jenkins Blair, A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368.1.sa0
Self-citation
Reviewer #3 (Public Review): Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
Clary Rachel, C., Jenkins Blair, A., & Lumpkin, E. A. (2023) · doi:10.7554/elife.87368.1.sa1
Self-citation
eLife Assessment: Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
Schuldiner, O. (2023) · doi:10.7554/elife.87368.1.sa4
TheAtoh1-CreKnock-In Allele Ectopically Labels a Subpopulation of Amacrine Cells and Bipolar Cells in Mouse Retina
Wu, S., & Zoghbi, H. Y. (2023) · eNeuro · doi:10.1523/eneuro.0307-23.2023
Ezh2 Delays Activation of Differentiation Genes During Normal Cerebellar Granule Neuron Development and in MedulloblastomaPreprint
Purzner, J., Brown, A. S., Purzner, T., Ellis, L., Broski, S., Litzenburger, U. M., Andrews, K., Sharma, A., Wang, X., Taylor, M. D., et al. (2025) · eLife · doi:10.7554/elife.105339
Intravital Two-Photon Imaging of Touch Sensory Axon Morphology in Mouse Skin
Kong, S., Barnes, E., Chelliah, G., & Meltzer, S. (2025) · Journal of Visualized Experiments · doi:10.3791/69589
Nucleolin is essential for hair cell stereocilia maintenance and auditory function in mice
Zong, W., Yan, K., Xing, H., et al. (2026) · Journal of Cell Science · doi:10.1242/jcs.264793
Guidage axonal commissural : mécanismes de sensibilisation au signal de la ligne médiane Sémaphorine 3B
Nawabi, H. (2009) · theses.fr (ABES) · doi:10.70675/deb0a9b9zc7a5z4312za23azbee7d3622018
Sensibilité des cellules de Merkel humaines au froid : vers un rôle des complexes de Merkel dans la sensibilité thermique cutanée ?
Roudaut, Y. (2014) · theses.fr (ABES) · doi:10.70675/f2fa3de4z968bz4505zbb2ez213c572cc0b7
La sensibilité au froid des cellules de Merkel et des kératinocytes, leurs contributions à la sensibiblité thermique et tactile de la peau
Bouvier, V. (2016) · theses.fr (ABES) · doi:10.70675/c5ef69a5zda1dz41d1z932az0bde098c793f
Etude de l'implication des cellules de Merkel dans l'initiation du prurit mécanique
Bataille, A. (2023) · theses.fr (ABES) · doi:10.70675/ba020e0dzb058z4c55za932za8b2a533f153

Authors: Lumpkin, E. A., Collisson, T., Parab, P., Omer-Abdalla, A., Haeberle, H., Chen, P., Doetzlhofer, A., White, P., Groves, A., Segil, N., & Johnson, J. E.
Affiliations: University of California, San Francisco (US)
The University of Texas Southwestern Medical Center (US)
House Clinic (US)
Corresponding author: Johnson, Jane E.
ORCID: Lumpkin, Ellen A.
Chen, Ping
Doetzlhofer, Angelika
Groves, Andrew
Segil, Neil
Johnson, Jane E.
Venue: Gene Expression Patterns
Publisher: Elsevier BV
Published: 2003-08
Volume: 3
Issue: 4
Pages: 389-395
ISSN: 1567-133X (ISSN-L)
DOI: 10.1016/s1567-133x(03)00089-9
OpenAlex: W1994624028
Cited by: 292
References: 30
Citations by year: 2026: 2 · 2025: 8 · 2024: 12 · 2023: 17 · 2022: 13 · 2021: 8 · 2020: 11 · 2019: 12 · 2018: 15 · 2017: 13 · 2016: 14 · 2015: 20 · 2014: 18 · 2013: 18 · 2012: 17
FWCI: 2.19
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Gene Expression Patterns (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute on Deafness and Other Communication Disorders (R01DC004189)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
Keywords: Math1, bHLH transcription factors, GFP reporter, transgenic mice, neural progenitor cells, dorsal interneurons, granule cell progenitors, cerebellum, Merkel cells, hair cells, vestibular system, auditory system, apical ectodermal ridge, dentate gyrus, retina, olfactory epithelium, brain development
MeSH terms: Animals, Cerebellum, Female, Interneurons, Lac Operon, Luminescent Proteins, Mice, Transgenic, Nerve Tissue Proteins, Pregnancy, Skin, Spinal Cord, Transcription Factors, In Situ Hybridization, Gene Expression Regulation, Developmental, Merkel Cells, Green Fluorescent Proteins, Mice, Basic Helix-Loop-Helix Proteins

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

Math1-driven GFP expression in the developing nervous system of transgenic mice

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks