Visualization of a short-range Wnt gradient in the intestinal stem-cell niche

Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche

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Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts

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Functional Repair of CFTR by CRISPR/Cas9 in Intestinal Stem Cell Organoids of Cystic Fibrosis Patients

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Small molecule–mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer

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The intestinal crypt, a prototype stem cell compartment

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Tissue‐specific and inducible Cre‐mediated recombination in the gut epithelium

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Tumour suppressor RNF43 is a stem-cell E3 ligase that induces endocytosis of Wnt receptors

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ZNRF3 promotes Wnt receptor turnover in an R-spondin-sensitive manner

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Structural Basis of Wnt Recognition by Frizzled

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Phosphorylation of PPDPF via IL6‐JAK2 activates the Wnt/β‐catenin pathway in colorectal cancer

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Characterizing the effects of triclosan and triclocarban on the intestinal epithelial homeostasis using small intestinal organoids

Cheng, X., Shen, H., Zhang, W., Chen, B., Xu, S., & Wu, L. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135734 · Cited by 16

Xenopus neural tube closure: A vertebrate model linking planar cell polarity to actomyosin contractions

Matsuda, M., & Sokol, S. Y. (2021) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2021.04.001 · Cited by 16

Unraveling the Control of Cell Cycle Periods during Intestinal Stem Cell Differentiation

Ballweg, R., Lee, S., Han, X., Maini, P. K., Byrne, H. M., Hong, C. I., & Zhang, T. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.10.025 · Cited by 16

Understanding Intratumoral Heterogeneity: Lessons from the Analysis of At-Risk Tissue and Premalignant Lesions in the Colon

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Mechano-Chemical Coupling in Hydra Regeneration and Patterning

Wang, R., Bialas, A. L., Goel, T., & Collins, E. S. (2023) · Integrative and Comparative Biology · doi:10.1093/icb/icad070 · Cited by 15

Sticking Around: Short-Range Activity of Wnt Ligands

Boutros, M., & Niehrs, C. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.02.018 · Cited by 15

Extracellular WNTs: Trafficking, Exosomes, and Ligand-Receptor Interaction.

Gross, J. C. (2021) · Handbook of Experimental Pharmacology · doi:10.1007/164_2021_531 · Cited by 12

The evolution of a new cell type was associated with competition for a signaling ligand

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The logistics of Wnt production and delivery

Alvarez‐Rodrigo, I., Willnow, D., & Vincent, J. (2023) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2023.01.006 · Cited by 12

Growth factors of stem cell niche extend the life-span of precision-cut intestinal slices in culture: A proof-of-concept study

Bigaeva, E., Bomers, J. J. M., Biel, C., Mutsaers, H. A. M., de Graaf, I. A. M., Boersema, M., & Olinga, P. (2019) · Toxicology in Vitro · doi:10.1016/j.tiv.2019.05.024 · Cited by 15

Regulation of stem and progenitor cells in the adrenal cortex

Finco, I., Mohan, D. R., Hammer, G. D., & Lerário, A. M. (2019) · Current Opinion in Endocrine and Metabolic Research · doi:10.1016/j.coemr.2019.07.009 · Cited by 14

Clonal analysis of stem cells in differentiation and disease

Colom, B., & Jones, P. H. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.07.002 · Cited by 13

From gut to glutes: The critical role of niche signals in the maintenance and renewal of adult stem cells

Trentesaux, C., Striedinger, K., Pomerantz, J. H., & Klein, O. D. (2020) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2020.01.004 · Cited by 15

Modelling adult stem cells and their niche in health and disease with epithelial organoids

Szabó, L., Seubert, A. C., & Kretzschmar, K. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.09.006 · Cited by 14

The Colonic Crypt: Cellular Dynamics and Signaling Pathways in Homeostasis and Cancer

Nguyen, A. L., Lausten, M. A., & Boman, B. M. (2025) · Cells · doi:10.3390/cells14181428 · Cited by 13

Sending signals – The microbiota’s contribution to intestinal epithelial homeostasis

Goyal, S., Tsang, D. K. L., Maisonneuve, C., & Girardin, S. E. (2020) · Microbes and Infection · doi:10.1016/j.micinf.2020.10.009 · Cited by 15

Leveraging Temporal Wnt Signal for Efficient Differentiation of Intestinal Stem Cells in an Organoid Model

Li, Y., Wang, X., Zhao, G., Deng, L., & Yin, X. (2023) · Stem Cells and Development · doi:10.1089/scd.2023.0186 · Cited by 14

Intestinal Paneth cell differentiation relies on asymmetric regulation of Wnt signaling by Daam1/2

Colozza, G., Lee, H., Merenda, A., Wu, S.-H. S., Català-Bordes, A., Radaszkiewicz, T. W., Jordens, I., Lee, J., Bamford, A.-D., Farnhammer, F., et al. (2023) · Science Advances · doi:10.1126/sciadv.adh9673 · Cited by 15

Ginseng promotes the function of intestinal stem cells through the Wnt/β-catenin signaling pathway in D-galactose-induced aging mice

Lu, G. U. O., Yan, R. Y., Zheng, D., Li, H., Li, G. L., & Wu, S. H. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112351 · Cited by 13

Identification and characterization of stem cells in mammalian esophageal stratified squamous epithelia

Yang, Y., Deng, G., Qiao, L., Yuan, H., Yu, X., Xu, L., Lu, S., Jiang, W. B., & Yu, X. (2022) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac038 · Cited by 13

Advancing intestinal organoid technology to decipher nano-intestine interactions and treat intestinal disease

Bao, L., Cui, X., Bai, R., & Chen, C. (2022) · Nano Research · doi:10.1007/s12274-022-5150-4 · Cited by 12

Using 3D Organoid Cultures to Model Intestinal Physiology and Colorectal Cancer

Short, S. P., Costacurta, P. W., & Williams, C. S. (2017) · Current Colorectal Cancer Reports · doi:10.1007/s11888-017-0363-8 · Cited by 14

New insights in ubiquitin-dependent Wnt receptor regulation in tumorigenesis

Tsukiyama, T. (2024) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-024-00855-w · Cited by 11

Small extracellular vesicles derived from umbilical cord mesenchymal stem cells alleviate radiation-induced cardiac organoid injury

Cao, H., Yue, L., Shao, J., Kong, F., Liu, S., Huai, H., He, Z., Mao, Z., Yang, Y., Tan, Y., et al. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-04115-2 · Cited by 15

Positional BMP signaling orchestrates villus length in the small intestine

Wang, X., Li, S., Liu, Y., Kuang, X., Chen, J., Yu, P., Zhao, L., Zhang, Z., Huang, M., Liu, L., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60643-2 · Cited by 13

Pluripotency state regulates cytoneme selectivity and self-organization of embryonic stem cells

Junyent, S., Reeves, J., Gentleman, E., & Habib, S. J. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202005095 · Cited by 12

Balance between the cell viability and death in 3D

Debruyne, A. C., Okkelman, I. A., & Dmitriev, R. I. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.09.005 · Cited by 16

Role of Wnt signaling in the maintenance and regeneration of the intestinal epithelium

Gasnier, M., Lim, H. Y. G., & Barker, N. (2023) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2023.01.001 · Cited by 14

Environmental Impact on Intestinal Stem Cell Functions in Mucosal Homeostasis and Tumorigenesis

Augenlicht, L. H. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25719 · Cited by 12

Dissecting the dynamics of signaling events in the BMP, WNT, and NODAL cascade during self-organized fate patterning in human gastruloidsPreprint

Chhabra, S., Liu, L., Goh, R., & Warmflash, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/440164 · Cited by 16

A 3D co-culture intestinal organoid system for exploring glucose metabolism

Nie, J., Liao, W., Zhang, Z., Zhang, M., Wen, Y., Çapanoğlu, E., Sarker, M. M. R., Zhu, R., & Zhao, C. (2022) · Current Research in Food Science · doi:10.1016/j.crfs.2022.11.021 · Cited by 11

General transcription factor TAF4 antagonizes epigenetic silencing by Polycomb to maintain intestine stem cell functions

Säisä-Borreill, S., Davidson, G., Kleiber, T., Thevenot, A., Martin, E., Mondot, S., Blottière, H. M., Helleux, A., Mengus, G., Plateroti, M., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-022-01109-6 · Cited by 11

M1 and M2 Macrophages Differentially Regulate Colonic Crypt Renewal

Raveenthiraraj, S., Awanis, G., Chieppa, M., O’Connell, A. E., & Sobolewski, A. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad270 · Cited by 11

Homeostasis, injury, and recovery dynamics at multiple scales in a self-organizing mouse intestinal crypt

Gall, L., Duckworth, C. A., Jardí, F., Lammens, L., Parker, A., Bianco, A., Kimko, H. H. C., Pritchard, D. M., & Pin, C. (2023) · eLife · doi:10.7554/elife.85478 · Cited by 12

Printable and biocompatible hydrogels for residual-free and high-throughput printing patient-derived organoid biochips

Xie, D., Chen, B., Xue, Y., Sun, Z., Ning, B., Zhang, Z., Chi, J., Su, M., & Song, Y. (2024) · Science China Materials · doi:10.1007/s40843-024-2933-8 · Cited by 11

Crosstalk Within the Intestinal Epithelium: Aspects of Intestinal Absorption, Homeostasis, and Immunity

Yu, L.-E., Yang, W., & Liang, Y. (2024) · Biomedicines · doi:10.3390/biomedicines12122771 · Cited by 13

Diffusion and function of Wnt ligands

Stewart, R. A., Ramakrishnan, A., & Cadigan, K. M. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008154 · Cited by 11

Biofunctional Nanodot Arrays in Living Cells Uncover Synergistic Co‐Condensation of Wnt Signalodroplets

Philippi, M., Richter, C. P., Kappen, M., Watrinet, I., Miao, Y., Runge, M., Jorde, L., Korneev, S., Holtmannspötter, M., Kurre, R., et al. (2022) · Small · doi:10.1002/smll.202203723 · Cited by 11

Direct visualization of the Wntless-induced redistribution of WNT1 in developing chick embryos

Galli, L. M., Santana, F., Apollon, C., Szabo, L. A., Ngo, K. J., & Burrus, L. W. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2018.04.025 · Cited by 13

Hmgcr promotes a long-range signal to attract Drosophila germ cells independently of Hedgehog

Kenwrick, K., Mukherjee, A., & Renault, A. D. (2019) · Journal of Cell Science · doi:10.1242/jcs.232637 · Cited by 11

Morphogen gradients are regulated by porous media characteristics of the developing tissue

Stark, J., Harish, R., Sbalzarini, I., & Brand, M. (2024) · bioRxiv · doi:10.1242/dev.204312 · Cited by 9

Cross-species comparison reveals therapeutic vulnerabilities halting glioblastoma progression

Foerster, L. C., Kaya, O., Wüst, V., Danciu, D.-P., Akcay, V., Bekavac, M., Ziegler, K. C., Stinchcombe, N., Tang, A., Kleber, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62528-w · Cited by 11

Tissue and cellular spatiotemporal dynamics in colon aging

Daly, A. C., Cambuli, F., Äijö, T., Lötstedt, B., Marjanovic, N. D., Fernandez, S., Kuksenko, O., Smith-Erb, M., Domovic, D., Wittenberghe, N. V., et al. (2025) · Nature Biotechnology · doi:10.1038/s41587-025-02830-6 · Cited by 11

Nectin-3 and shed forms of CSPG4 can serve as epithelial cell receptors for Clostridioides difficile TcdB

Childress, K. O., Cencer, C. S., Tyska, M. J., & Lacy, D. B. (2023) · mBio · doi:10.1128/mbio.01857-23 · Cited by 10

Nucleolin Targeting by N6L Inhibits Wnt/β-Catenin Pathway Activation in Pancreatic Ductal Adenocarcinoma

Raineri, F., Bourgoin‐Voillard, S., Cossutta, M., Habert, D., Ponzo, M., Houppe, C., Vallée, B., Boniotto, M., Chalabi‐Dchar, M., Bouvet, P., et al. (2021) · Cancers · doi:10.3390/cancers13122986 · Cited by 10

Taking a Step Back: Insights into the Mechanisms Regulating Gut Epithelial Dedifferentiation

Ouladan, S., & Gregorieff, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137043 · Cited by 9

Microbial Genes, Enzymes, and Metabolites: To Improve Rhizosphere and Plant Health Management

Fazeli‐Nasab, B., & Rahmani, A. F. (2021) · Springer eBooks · doi:10.1007/978-981-16-2922-8_19 · Cited by 11

Shifting the Focus of Signaling Abnormalities in Colon Cancer

Brown, M. A., & Ried, T. (2022) · Cancers · doi:10.3390/cancers14030784 · Cited by 11

Single-Molecule Imaging of Wnt3A Protein Diffusion on Living Cell Membranes

Lippert, A. H., Janeczek, A. A., Fürstenberg, A., Ponjavic, A., Moerner, W. E., Nusse, R., Helms, J. A., Evans, N. D., & Lee, S. F. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.08.060 · Cited by 10

Dickkopf-1 blocks 17β-estradiol-enhanced object memory consolidation in ovariectomized female mice

Taxier, L. R., Philippi, S. M., Fortress, A. M., & Frick, K. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.06.009 · Cited by 10

Changes in epithelial proportions and transcriptional state underlie major premenopausal breast cancer risksPreprint

Murrow, L. M., Weber, R. J., Caruso, J. A., McGinnis, C. S., Phong, K. T., Gascard, P. D., Borowsky, A. D., Desai, T. A., Thomson, M., Tlsty, T. D., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/430611 · Cited by 11

The TMEM63B Channel Facilitates Intestinal Motility and Enhances Proliferation of Intestinal Stem Cells

Tu, J.-J., Zang, Y., Shi, Y. S., & Teng, X. (2024) · Cells · doi:10.3390/cells13211784 · Cited by 10

Foxo3-mediated physiological cell competition ensures robust tissue patterning throughout vertebrate development

Matsumoto, K., Akieda, Y., Haraoka, Y., Hirono, N., Sasaki, H., & Ishitani, T. (2024) · Nature Communications · doi:10.1038/s41467-024-55108-x · Cited by 9

Long-range organization of intestinal 2D-crypts using exogenous Wnt3a micropatterning

Larrañaga, E., Marín-Riera, M., Abad‐Lázaro, A., Bartolomé-Català, D., Otero-Tarrazón, A., Fernández‐Majada, V., Batlle, E., Sharpe, J. A., Ojosnegros, S., Comelles, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-55651-7 · Cited by 9

Genetically encoded affinity reagents are a toolkit for visualizing and manipulating endogenous protein function in vivo

Boswell, C. W., Hoppe, C., Sherrard, A., Miao, L., Kojima, M. L., Martino, P. A., Zhao, N., Stasevich, T. J., Nicoli, S., & Giráldez, A. J. (2025) · Nature Communications · doi:10.1038/s41467-025-61003-w · Cited by 9

Roles of intestinal stem cells in inflammatory bowel disease pathogenesis

Zhang, M.-J., Chan, S.-X., Jia, Z.-G., Lv, C., Chen, J., & Hong, S. (2025) · World Journal of Stem Cells · doi:10.4252/wjsc.v17.i8.107639 · Cited by 10

WNT16 from decidual stromal cells regulates HTR8/SVneo trophoblastic cell function via AKT/beta-catenin pathway

Li, X., Shi, J., Zhao, W., Huang, X., Cui, L., Liu, L., Jin, X., Li, D., Zhang, X., & Du, M. (2022) · Reproduction · doi:10.1530/rep-21-0282 · Cited by 9

Transfer of polarity information via diffusion of Wnt ligands in C. elegans embryos

Recouvreux, P., Pai, P., Dunsing, V., Torro, R., Ludányi, M., Mélénec, P., Boughzala, M., Bertrand, V., & Lenne, P. (2024) · Current Biology · doi:10.1016/j.cub.2024.03.030 · Cited by 9

Manipulation of focal Wnt activity via synthetic cells in a double‐humanized zebrafish model of tumorigenesis

Wang, L., Long, J., Chen, H., Sun, S., Lv, K., Li, Q., & Wang, X. (2020) · International Journal of Cancer · doi:10.1002/ijc.33458 · Cited by 9

A model of neocortical area patterning in the lissencephalic mouse may hold for larger gyrencephalic brains

Jones, W. D., Guadiana, S. M., & Grove, E. A. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24643 · Cited by 9

Spatially defined microenvironment for engineering organoids

Zhang, Y., Qi, F., Chen, P., Liu, B., & Li, Y. (2024) · Biophysics Reviews · doi:10.1063/5.0198848 · Cited by 9

The IL-18 receptor is expressed on murine small-intestinal enterochromaffin cells and executes a recovery program upon injury

Winsor, N. J., Tsang, D. K. L., Ranger, A., Singh, O., Goyal, S., Philpott, D. J., & Girardin, S. E. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2417149122 · Cited by 9

Telocytes deliver essential Wnts directly to murine intestinal stem cells via synapse-like contacts

Greicius, G., Mittermeier, L., Liang, R., Sigmundsson, K., Chan, Y. K., Liao, P.-J., Ludwig, A., & Virshup, D. M. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.06.040 · Cited by 8

Triple‐Decker Sandwich Cultures of Intestinal Organoids for Long‐Term Live Imaging, Uniform Perturbation, and Statistical Sampling

Cambra, H. M., Tallapragada, N. P., Mannam, P., Breault, D. T., & Klein, A. M. (2022) · Current Protocols · doi:10.1002/cpz1.330 · Cited by 8

The Relationship between LRP6 and Wnt/β-Catenin Pathway in Colorectal and Esophageal Cancer

Shishido, A., Miyo, M., Oishi, K., Nishiyama, N., Wu, M., Yamamoto, H., Kouda, S., Wu, X., Shibata, S., Yokoyama, Y., et al. (2023) · Life · doi:10.3390/life13030615 · Cited by 11

Biased precursor ingression underlies the center-to-pole pattern of male sex determination in mouse

Bunce, C., Barske, L. A., Zhang, G. X., & Capel, B. (2023) · Development · doi:10.1242/dev.201060 · Cited by 8

Spatial regulation of Drosophila ovarian Follicle Stem Cell division rates and cell cycle transitions

Melamed, D., Choi, A., Reilein, A. R., Tavaré, S., & Kalderon, D. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010965 · Cited by 7

Wg secreted by conventional Golgi transport diffuses and forms Wg gradient whereas Wg tethered to extracellular vesicles do not diffuse

Won, J.-H., & Cho, K.-O. (2020) · Cell Death and Differentiation · doi:10.1038/s41418-020-00632-8 · Cited by 8

Building bridges between fields: bringing together development and homeostasis

Weterings, S. D. C., van Oostrom, M. J., & Sonnen, K. F. (2021) · Development · doi:10.1242/dev.193268 · Cited by 10

Roads to the Fountain of Youth? Rejuvenating Intestinal Stem Cells

Larrick, J. W., & Mendelsohn, A. R. (2019) · Rejuvenation Research · doi:10.1089/rej.2019.2251 · Cited by 9

An Overview on the Pharmaceutical Applications of Nanocellulose

Kamel, R., & ElKasabgy, N. A. (2023) · Composites science and technology · doi:10.1007/978-981-99-2473-8_13 · Cited by 7

Modulation of the canonical Wnt activity by androgen signaling in prostate epithelial basal stem cells

Horton, C., Liu, Y., Wang, J., Green, J., Tsyporin, J., Chen, B., & Wang, Z. A. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.04.003 · Cited by 11

Stem cell development involves divergent thyroid hormone receptor subtype expression and epigenetic modifications in the Xenopus metamorphosing intestine

Hasebe, T., Fujimoto, K., Buchholz, D. R., & Ishizuya‐Oka, A. (2020) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2020.113441 · Cited by 7

A new gain‐of‐function mouse line to study the role of Wnt3a in development and disease

Chalamalasetty, R. B., Ajima, R., Garriock, R. J., Kennedy, M. W., Tessarollo, L., & Yamaguchi, T. P. (2016) · genesis · doi:10.1002/dvg.22959 · Cited by 6

Active β-Catenin Signaling in the Small Intestine of Humans During Infancy

Dudhwala, Z. M., Drew, P. A., Howarth, G. S., Moore, D., & Cummins, A. G. (2018) · Digestive Diseases and Sciences · doi:10.1007/s10620-018-5286-y · Cited by 6

Cre-Recombinase Induces Apoptosis and Cell Death in Enterocyte Organoids

Moll, F., Spaeth, M., & Schröder, K. (2022) · Antioxidants · doi:10.3390/antiox11081452 · Cited by 6

Small-molecule probe reveals a kinase cascade that links stress signaling to TCF/LEF and Wnt responsiveness

Cheng, J., Tsuda, M., Okolotowicz, K. J., Dwyer, M., Bushway, P., Colas, A. R., Lancman, J. J., Schade, D., Perea‐Gil, I., Bruyneel, A. A. N., et al. (2021) · Cell chemical biology · doi:10.1016/j.chembiol.2021.01.001 · Cited by 7

Real‐Time Analysis of Endogenous Wnt Signalling in 3D Mesenchymal Stromal Cells

Saleh, F., Carstairs, A., Etheridge, S. L., & Genever, P. G. (2016) · Stem Cells International · doi:10.1155/2016/7132529 · Cited by 6

Notch inhibition counteracts Paneth cell death in absence of caspase-8

Jeon, M., Kaemmerer, E., Schneider, U., Schiffer, M., Klaus, C., Hennings, J., Clahsen, T., Ackerstaff, T., Niggemann, M., Schippers, A., et al. (2018) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-018-2368-3 · Cited by 7

Characteristic, Regulation and Targeting Strategies of Cancer Stem Cells and Their Niche in Digestive System Tumors

Chen, Z., Qi, H., Xue, Y., Zhang, Y., Zhang, Z., Xu, S., Liao, S., Zeng, X., Wu, J., Lv, X., et al. (2025) · MedComm – Oncology · doi:10.1002/mog2.70015 · Cited by 6

Insights from tissue “omics” analysis on intestinal remodeling in celiac disease

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Dickkopf1 induces enteric neurogenesis and gliogenesis in vitro if apoptosis is evaded

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ORIGINAL ARTICLE

Tomlinson, I. P. M. (2016)