The intestinal stem cell

Identification of human brain tumour initiating cells

Singh, S. K., Hawkins, C. E., Clarke, I. D., Squire, J. A., Bayani, J., Hide, T., Henkelman, R. M., Cusimano, M. D., & Dirks, P. B. (2004) · Nature · doi:10.1038/nature03128 · Cited by 7,564

Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell

Bonnet, D. A., & Dick, J. E. (1997) · Nature Medicine · doi:10.1038/nm0797-730 · Cited by 7,197

Identification of stem cells in small intestine and colon by marker gene Lgr5

Barker, N., van Es, J. H., Kuipers, J., Kujala, P., van den Born, M., Cozijnsen, M., Haegebarth, A., Korving, J., Begthel, H., Peters, P. J., et al. (2007) · Nature · doi:10.1038/nature06196 · Cited by 5,687

A human colon cancer cell capable of initiating tumour growth in immunodeficient mice

O'Brien, C. A., Pollett, A. F., Gallinger, S., & Dick, J. E. (2006) · Nature · doi:10.1038/nature05372 · Cited by 4,174

Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC

Morin, P. J., Sparks, A. B., Kořínek, V., Barker, N., Clevers, H. C., Vogelstein, B., & Kinzler, K. W. (1997) · Science · doi:10.1126/science.275.5307.1787 · Cited by 4,000

Purification and Characterization of Mouse Hematopoietic Stem Cells

Spangrude, G. J., Heimfeld, S., & Weissman, I. L. (1988) · Science · doi:10.1126/science.2898810 · Cited by 2,908

Constitutive Transcriptional Activation by a β-Catenin-Tcf Complex in APC −/− Colon Carcinoma

Korinek, V., Barker, N., Morin, P. J., van Wichen, D., de Weger, R., Kinzler, K. W., Vogelstein, B., & Clevers, H. (1997) · Science · doi:10.1126/science.275.5307.1784 · Cited by 2,905

Phenotypic characterization of human colorectal cancer stem cells

Dalerba, P. D., Dylla, S. J., Park, I.-K., Liu, R., Wang, X., Cho, R. W., Hoey, T., Gurney, A. L., Huang, E. H., Simeone, D. M., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703478104 · Cited by 2,237

Identification of a subpopulation of cells with cancer stem cell properties in head and neck squamous cell carcinoma

Prince, M. E., Sivanandan, R., Kaczorowski, A., Wolf, G. T., Kaplan, M. J., Dalerba, P. D., Weissman, I. L., Clarke, M. F., & Ailles, L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610117104 · Cited by 2,205

Defining the Epithelial Stem Cell Niche in Skin

Tumbar, T., Guasch, G., Greco, V., Blanpain, C., Lowry, W. E., Rendl, M., & Fuchs, E. (2004) · Science · doi:10.1126/science.1092436 · Cited by 2,031

Epithelial progenitor 1, a novel factor associated with epithelial cell growth and differentiation

Kritzik, M. R., Lago, C. U., Kayali, A. G., Dabernat, S., Liu, G., Zhang, Y.-Q., Hua, H., Fox, H. S., & Sarvetnick, N. (2010) · Endocrine · doi:10.1007/s12020-009-9297-5 · Cited by 2

Rising from the crypt: decreasing DNA methylation during differentiation of the small intestine

Cullen, S. M., & Goodell, M. A. (2013) · Genome biology · doi:10.1186/gb-2013-14-5-116 · Cited by 2

The Role of Hippo Signaling in Intestinal Homeostasis

Ma, X., & Shah, Y. M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00005-0 · Cited by 2

Chapter 8 Dietary fibre, gut sensing and modulation of feed intake in pigs and chickens

Roura, E. (2019) · Wageningen Academic Publishers eBooks · doi:10.3920/978-90-8686-893-3_8 · Cited by 3

Flow, Mixing and Absorption at the Mucosa

Lentle, R. G., & Janssen, P. W. M. (2011) · Springer eBooks · doi:10.1007/978-1-4419-9449-3_10 · Cited by 2

Rosa26-GFP Direct Repeat (RaDR-GFP) Mice Reveal Tissue- and Age-Dependence of Homologous Recombination in Mammals In Vivo

Sukup-Jackson, M. R., (5659234), O. K., Kay, J. E., Na, L., Rowland, E. A., Winther, K. E., Chow, D. N., Kimoto, T., Matsuguchi, T., Jonnalagadda, V. S., et al. (2016) · Figshare · doi:10.1371/journal.pgen.1004299 · Cited by 50

From anatomy to immunity in the gastrointestinal system

Menéndez, A., & Guttman, J. A. (2023) · The Anatomical Record · doi:10.1002/ar.25188 · Cited by 1

Partial efficacy of Yuzu (Citrus junos) pectin side chains in elongating the jejunal villus in protein-deficient malnourished mice

Masuda, R., Gotoh, S., Othman, S. B., Kitaguchi, K., & Yabe, T. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106454 · Cited by 1

Intestinal mucosal turnover in germ-free piglets infected with E. coli

Tóth, Š., Fagová, Z., Holodová, M., Čurgali, K., Mechírová, E., Kunová, A., Maretta, M., Nemcová, R., Gancarčíková, S., & Danková, M. (2024) · Journal of Molecular Histology · doi:10.1007/s10735-024-10278-2 · Cited by 1

Circular RNAs in Intestinal Mucosal Homeostasis and Pathologies

Chung, H. K., Xiao, L., & Wang, J.-Y. (2026) · Non-Coding RNA · doi:10.3390/ncrna12030014 · Cited by 1

Establishing Murine Intestinal Organoids to Study Nutrient- and Tastant-Evoked Gut Signaling

Kumar, P., Ziegler, F., & Behrens, M. (2026) · Nutrients · doi:10.3390/nu18121995 · Cited by 1

Pharmacogenomic assessment of an acute colitis model

Roca, J., Camacho, H., Guillen, I., Aguilera, A., Palenzuela, D., Silva, J., Estrada, R., Gell, O., Berlanga, J., & Novoa, L. (2018) · Bionatura · doi:10.21931/rb/2018.03.02.3 · Cited by 1

Bibliometric insights into the cell cycle, aging, and metabolism: from molecular mechanisms to clinical implications

Pan, Y., Liu, H., Chen, J., Deng, H., Yang, C., Huang, Y., Cai, Q., Huang, W., Huang, M., Xiong, S., et al. (2025) · Biogerontology · doi:10.1007/s10522-025-10271-6 · Cited by 1

A common food mutagen promotes intestinal carcinogenesis by multiple mechanisms in mouse models of Lynch syndrome

Rayner, E., Tsaalbi‐Shtylik, A., Marques, L., Agaser, C., Mei, H., Cats, D., van Zanen-Gerhardt, S., Salvatori, D. C. F., & de Wind, N. (2025) · NAR Cancer · doi:10.1093/narcan/zcaf045 · Cited by 1

PRX5 as a critical driver of colorectal cancer stemness and tumorigenicity

Lee, S. W., Park, S.-J., Lee, G. S., Jung, S.-M., 이재연, Kwon, S., Yeom, E., Lee, D.-S., & Choi, E.-H. (2026) · Redox Report · doi:10.1080/13510002.2026.2673661 · Cited by 1

Self-renewal and Differentiation of Intestinal Stem Cells: Role of Hedgehog Pathway

Büller, N. V. J. A., Rosekrans, S. L., & BRINK, G. R. V. D. (2011) · Springer eBooks · doi:10.1007/978-94-007-2016-9_10 · Cited by 1

Where intestinal epithelial stem cells are localized? About molecular markers

Proskuryakov, S. Y., Konoplyannikov, A. G., Verkhovskii, Y. G., Ulyanova, L. P., & Tsyb, A. F. (2011) · Biochemistry (Moscow) Supplement Series B Biomedical Chemistry · doi:10.1134/s1990750811010100 · Cited by 1

Stem-like cells in colorectal oncology.

Tomuleasa, C., Șușman, S., Şoriţău, O., Moșteanu, O., Pop, T., Petrushev, B., Kacsó, G., Buiga, R., Tantau, M. V., & Irimie, A. I. (2011) · PubMed · Cited by 1

The Normal Biopsy: Colonic and Ileal Mucosa and Submucosa

Jouret‐Mourin, A., Eyken, P. V., Leo, M., & Geboes, K. (2018) · Springer eBooks · doi:10.1007/978-3-319-89503-1_2 · Cited by 1

Dynamical Modeling of Stem Cell Regeneration

Lei, J. (2021) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-3-030-73033-8_6 · Cited by 1

Changes in equine intestinal stem/progenitor cell number at resection margins in cases of small intestinal strangulation

Veerasammy, B. A., Gonzalez, G. A., Báez‐Ramos, P., Schaaf, C. R., Stewart, A. S., Ludwig, E. K., McKinney, C. A., Freund, J. M., Robertson, J. B., & Gonzalez, L. M. (2023) · Equine Veterinary Journal · doi:10.1111/evj.13927 · Cited by 1

Scribble deficiency mediates colon inflammation by inhibiting autophagy-dependent oxidative stress elimination

Sun, X., Lu, L., Wang, K., Song, L., Jiao, J., Wu, Y., Wang, X., Song, Y., & Zhan, L. (2023) · Scientific Reports · doi:10.1038/s41598-023-45176-2 · Cited by 1

Large animal models enhance the study of crypt-mediated epithelial recovery from prolonged intestinal ischemia reperfusion injury

McKinney, C. A., Schaaf, C. R., Goya‐Jorge, E., Freund, J. M., & Gonzalez, L. M. (2024) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00236.2024 · Cited by 1

Stem Cell Based Therapy for Lung Disease Preclinical evidence for the role of stem/stromal cells Clinical application of stem/stromal cells in lung fibrosis

Patete, C. L., Toonkel, R. L., & Glassberg, M. K. (2019) · Springer eBooks · doi:10.1007/978-3-030-29403-8_7 · Cited by 1

A further study on a disturbance of intestinal epithelial cell population and kinetics in APC1638T mice

Wenduerma, Yamada, N. O., Wang, T., & Senda, T. (2021) · Medical Molecular Morphology · doi:10.1007/s00795-020-00279-x · Cited by 1

Environmental Interaction and Impact on the Life Span of Stem Cells

Kumar, A., Jain, K. G., & Arora, V. (2020) · Springer eBooks · doi:10.1007/978-981-15-7493-1_12 · Cited by 1

Protein Biomarkers Of Cell Proliferation Determine Prognosis In Cases Of Equine Large Colon Volvulus

(2017) · Equine Veterinary Education · doi:10.1111/eve.80_12792 · Cited by 1

Epithelial Reparative Capacity Regulates Extracellular Matrix Dynamics and Innate Immunity

Snyder, J. C. (2009) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

Biomechanical modelling of colorectal crypt formation and in-vitro replication

Nelson, M. R. (2011) · Nottingham ePrints (University of Nottingham) · Cited by 1

Defining innate immunity to Clostridium difficile

Jafari, N. V. (2012) · UCL Discovery (University College London) · Cited by 1

Wnt Signaling Regulation of Tissue Architecture (EMT and MET) and Morphogenesis

Fifis, T., Tran, B. M., Schwab, R., Johanson, T. M., Warner, N., Barker, N., & Vincan, E. (2014) · Wiley eBooks · doi:10.1002/9781118444122.ch24 · Cited by 1

Elucidating the role of the mucus-associated microbiota and mucin glycosylation in inflammatory bowel disease

Thursby, E. (2016) · UEA Digital Repository (University of East Anglia) · Cited by 1

Doublecortin-like kinase 1 as a novel drug target and biomarker in gastrointestinal and renal cancers

Weygant, N. (2018) · Cited by 1

Critical Regulators of Epithelial Homeostasis and Intestinal Crypt Regeneration: Identification of Novel BVES/BCAR3 Signaling Complex in EMT and Tumorigenesis and Biological Implications for MTG16 in Stem Cell Function, Proliferation, Apoptosis and DNA Repair.

Poindexter, S. V. (2015) · Cited by 1

Impact of polyphenols and feeding rhythms on the immunomodulation properties of the probiotic bacteria in the gastro-intestinal tract

Tarraf, A. A. (2021) · theses.fr (ABES) · doi:10.70675/545bd347z20bcz444cza534z622ac595baf9 · Cited by 1

Stem Cells and Alcohol-Related Cancers

Gao, Z. P., & Guo, Q. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0040-0_11

Drug Resistance Mechanisms to Gamma-secretase Inhibitors in Human Colon Cancer Cells

Timme, C. R. (2013) · Digital Commons - University of South Florida (University of South Florida)

Development, Structure, and Function of the Tubal Gut

Bosman, F. T., & Yan, P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-386456-7.03801-6

Effects of age and Pax6 deficiency on mouse limbal stem cell function

Douvaras, P. (2010) · ERA

Regeneration After Injury: Activation of Stem Cell Stress Response Pathways to Rapidly Repair Tissues

Paulson, R. F., Bennett, L. F., & Xiang, J. (2013) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4614-9569-7_16

Phenotype and function of intestinal CD103+ dendritic cells

Gyllenbäck, E. J. (2011) · Lund University Publications (Lund University)

Inflammatory bowel diseases and intestinal epithelial stem cells

Watanabe, M. (2012) · Inflammation and Regeneration · doi:10.2492/inflammregen.32.039

Epithelial cells transdifferentiation into bladder urothelium in experiments in vivo

Popov, B. V., Zaichik, A. M., Budko, M. B., Злобина, О. В., Tolkunova, E. N., Zhidkova, O. V., & Ns, P. (2011) · Cell and Tissue Biology · doi:10.1134/s1990519x11040079

Stem Cell in Pediatric Gastrointestinal Tract Disease: Hirschsprung Disease

Bae, S. H. (2011) · Korean Journal of Pediatric Gastroenterology and Nutrition · doi:10.5223/kjpgn.2011.14.suppl1.s42

Isolated ileal interposition in enteroendocrine L cells differentiationPreprint

Azevedo, J.-L., Neves, K., Azevedo, J., Bernardes, L., de Azevedo, O. C., Aguiar-Yamaguchi, G., Miguel, G. P. S., Cardia, W., Marigliani, B., Azevedo, J.-L., et al. (2011) · Nature Precedings · doi:10.1038/npre.2011.6614.2

Mucus and mucins during gastrointestinal infections

Navabi, N. (2014) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Epithelial regeneration by transplantation of cultured intestinal stem cells

Nakamura, T. (2015) · Inflammation and Regeneration · doi:10.2492/inflammregen.35.019

A network in the intestinal protective mucus

Johansson, M. (2009)

Epithelial to Mesenchymal Transition (EMT) and Intestinal Tumorigenesis

Pulkoski‐Gross, A., Zheng, X., Kim, D., Cathcart, J. M., & Cao, J. P. (2015) · Springer eBooks · doi:10.1007/978-3-319-19986-3_11

Intracellular Mechanisms Responsible for Trypsin-induced Increase in Transepithelial Resistance in Intestinal Epithelial Cells

Wadhwani, A. (2013) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/26622

Drosophila as a Model for Analyzing of Human Genetic and Pathogenic Related Diseases

Hossain, M. S. (2015)

Molecular characterization of pluripotency in embryos and embryonic stem cells

Gómez, J. P. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Role of Prolactin and Prolactin Receptor Signaling in Colorectal Tumorigenesis

Neradugomma, N. K. (2014) · KU ScholarWorks (The University of Kansas)

Mapping Function and Cooperativity in the Cancer Genome: RSPO2 and WAC

Conboy, C. B. (2014) · University of Minnesota Digital Conservancy (University of Minnesota)

Colon stem cell characterization in normal and tumoral tissues: description of a novel feed-forward circuit of Msi-1 regulation

Pastò, A. (2013) · Padua@research (University of Padova)

Characterization of human colorectal cancer stem cells and their role in chemoresistance

Butler, S. J. (2015) · The Atrium (University of Guelph)

Further studies support the participation of stem cells in the cell turnover of duodenal adenomas.

Rubio‐Terres, C. (2009) · PubMed

Lung Vascular Regeneration and Repair

Yöder, M. C., & Thébaud, B. (2015) · Stem cell biology and regenerative medicine · doi:10.1007/978-3-319-21082-7_15

A study on immunomodulating beta-glucan: Effects of oral application on inflammation, tissue injury, and the mucosal immune system in experimental animals

Sandvik, A. (2009) · NORA - Norwegian Open Research Archives

Epithelial Progenitor Cells of the Mammalian Lung

Teisanu, R. M., Snyder, J. C., & Stripp, B. R. (2010) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781848164406_0004

Transcriptional regulation of slc6a19 along the crypt-villus axis

Tümer, E. (2016) · ANU Open Research (Australian National University) · doi:10.25911/5d778afa0a920

Where intestinal epithelial stem cells are localized? About molecular markers

Proskuryakov, S. Y., Konoplyannikov, A. G., Verkhovskii, Y. G., Ulyanova, L. P., & Tsyb, A. F. (2011) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20115704359

An investigation of ADAM-like Decysin 1 in macrophage-mediated inflammation and Crohn's Disease

O’Shea, N. R. (2016) · UCL Discovery (University College London)

Research applications of intestinal organoids in precision medicine

JianJun, G. A. O., Chu, W. A. N. G., & GuoQiang, H. U. A. (2017) · Scientia Sinica Vitae · doi:10.1360/n052016-00342

Novel Enteroendocrine Cell Receptors Regulating Incretin Secretion and Glucose Homeostasis

Flock, G. B. (2012) · TSpace (University of Toronto)

Novel Cell Therapies and Manipulations: Ready for Prime-Time?

(2017) · Cambridge University Press eBooks · doi:10.1017/9781316335727.063

Regenerative Medicine: The Future?

Atkinson, K. (2017) · Cambridge University Press eBooks · doi:10.1017/9781316335727.069

Growth Differentiation Factor 11 does not Mitigate the Lethal Effects of Total-Abdominal Irradiation

Duhachek-Muggy, S., Bhat, K., Vlashi, E., & Pajonk, F. (2017) · Radiation Research · doi:10.1667/rr14628.1

The regulation of cancer cachexia and colorectal carcinogenesis by myostatin

Wijesoma, I. W. (2017) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/72527

Short mononucleotide repeat detection of MSI : towards high throughput diagnosis

Redford, L. (2016)

USE OF PEA PROTEIN-POLYSACCHARIDE MICROCAPSULES AS A DELIVERY SYSTEM FOR PROBIOTIC BACTERIA; TESTING UNDER SIMULATED GASTRIC CONDITIONS AND IN ANIMAL MODEL SYSTEMS

Varankovich, N. V. (2017) · University Library - University of Saskatchewan (University of Saskatchewan)

Demise of lung transplants: exposing critical gaps in understanding lung stem cells

Xian, W., & McKeon, F. (2018) · Journal of Thoracic Disease · doi:10.21037/jtd.2018.03.146

Microbiome and Gut Immunity: The Epithelium

Günther, C. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_7

Characterisation of mouse duodenal cholecystokinin cell

Huang, X. (2014) · Research Explorer (The University of Manchester)

Developing models of the small intestine

Dosh, R. H. (2018) · Sheffield Hallam University · doi:10.7190/shu-thesis-00131

Side Population Sorting Separates Subfractions of Intestinal Stem Cells

von Furstenberg, R. J. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/n1af-rd47

Isolation of Gut, Imaginal Disc, Fat Body, Ovary and Testes in Various Developmental Stages of Drosophila

Nayak, N., Dhar, G., & Mishra, M. (2019) · Springer protocols handbooks/Springer protocols · doi:10.1007/978-1-4939-9756-5_2

An in vivo and in vitro Investigation of Glycerol Utilization in Intestinal Triacylglycerol Metabolism.

Lou, S. (2013) · Surrey Research Insight Open Access (The University of Surrey)

Understanding the Effects of Antibiotic Exposure on Host Immune-Microbiota Crosstalk and the Development of Colitis

Goethel, A. (2017) · TSpace (University of Toronto)

Potential of embryonic stem cells for treating intestinal diseases

El-Hashash, A. H. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821269-1.00001-1

Role of Notch Signalling in Oxidative Stress and Stem Cell Self-Renewal During Colitis and Colon Cancer

Andrabi, M. Q., & Ramalingam, S. (2022) · Handbook of Oxidative Stress in Cancer: Therapeutic Aspects · doi:10.1007/978-981-16-1247-3_82-1

Role of Notch Signalling in Oxidative Stress and Stem Cell Self-Renewal During Colitis and Colon Cancer

Andrabi, M. Q., & Ramalingam, S. (2022) · Handbook of Oxidative Stress in Cancer: Therapeutic Aspects · doi:10.1007/978-981-16-5422-0_82

Nutrition and Degenerative Brain Dysfunctions

Bell, V., & Fernandes, T. H. (2023) · European journal of applied sciences · doi:10.14738/aivp.111.13720

Introduction on Stem Cell Therapy and Regeneration

Masrour, M., Moeinafshar, A., & Rezaei, N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15717-2.00059-7

Additional file 1 of Colonic stem cells from normal tissues adjacent to tumor drive inflammation and fibrosis in colorectal cancer

Zhao, Y., Guo, M., Zhao, F.-Q., Liu, Q., & Wang, X. (2023) · Figshare · doi:10.6084/m9.figshare.23819953

Additional file 2 of Colonic stem cells from normal tissues adjacent to tumor drive inflammation and fibrosis in colorectal cancer

Zhao, Y., Guo, M., Zhao, F.-Q., Liu, Q., & Wang, X. (2023) · Figshare · doi:10.6084/m9.figshare.23819956

A Novel Use of Embryonic Gut Organoid Culture to Investigate Duodenal Atresia

Jones, M. L. M., Sarila, G., O'Sullivan, B., Haycock, S., Chapuis, P. H., King, S. K., & Teague, W. J. (2024) · Journal of Pediatric Surgery · doi:10.1016/j.jpedsurg.2024.06.020

Clinical and immunohistochemical studies of small bowel carcinoid tumours

Landerholm, K. (2011) · DiVA (Linkoping University)

The Effect of Inflammation on Stem Cell Mutagenesis and Carcinogenesis Induced by Azoxymethane in Wild type and Immune Compromised Mice

Whetstone, R. D. (2014) · D-Scholarship@Pitt (University of Pittsburgh)

Wnt signalling and EphB-ephrin interactions in intestinal stem cells and CRC progression

Batlle, E. (2008)

Additional file 25 of Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium

Kazakevych, J., Denizot, J., Liebert, A., Portovedo, M., Mosavie, M., Jain, P., Stellato, C., Fraser, C. M., Corrêa, R. O., Célestine, M., et al. (2020) · Figshare · doi:10.6084/m9.figshare.11972577

Additional file 1 of Vitamin D3 suppresses intestinal epithelial stemness via ER stress induction in intestinal organoids

Sittipo, P., Kim, H. K., Han, J., Lee, M. R., & Lee, Y. K. (2021) · Figshare · doi:10.6084/m9.figshare.14594457

Additional file 3 of Colonic stem cells from normal tissues adjacent to tumor drive inflammation and fibrosis in colorectal cancer

Zhao, Y., Guo, M., Zhao, F., Liu, Q., & Wang, X. (2023) · Figshare · doi:10.6084/m9.figshare.23819959

Additional file 4 of Colonic stem cells from normal tissues adjacent to tumor drive inflammation and fibrosis in colorectal cancer

Zhao, Y., Guo, M., Zhao, F., Liu, Q., & Wang, X. (2023) · Figshare · doi:10.6084/m9.figshare.23819962

Additional file 1 of Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium

Kazakevych, J., Denizot, J., Liebert, A., Portovedo, M., Mosavie, M., Jain, P., Stellato, C., Fraser, C. M., Corrêa, R. O., Célestine, M., et al. (2020) · Figshare · doi:10.6084/m9.figshare.11972538

Additional file 26 of Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium

Kazakevych, J., Denizot, J., Liebert, A., Portovedo, M., Mosavie, M., Jain, P., Stellato, C., Fraser, C. M., Corrêa, R. O., Célestine, M., et al. (2020) · Figshare · doi:10.6084/m9.figshare.11972583

Molecular and Chromatin Accessibility Programs Underlying Epithelial Injury and Impaired Regeneration in Neonatal Necrotizing Enterocolitis

Xiong, Y., Zito, A., Liang, H., Biouss, G., Yang, J., Balsamo, F., Yeganeh, M., Lee, C., Lee, D., Wang, C.-Y., et al. (2026) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2026.101730 · Cited by 3

Myosin VB is critical for progenitor cell identity and function in the intestine

Burman, A., Brown, M. E., Yang, Y., Momoh, M., Adeniran, F., Ramos, C., Lau, K. S., Samuelson, L. C., Shub, M. D., Roland, J. T., et al. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.102820

A Rare T-Cell Factor 4 Lineage-negative Epithelial Stem Cell Supports Wound Repair and APC-deletion-induced Colon TumorigenesisPreprint

Thorpe, A. V., Mosbruger, T., Georges, S. J., Crowley, O. M., Tuohy, T. M. F., Dalley, B. K., Bice, B. D., Fuller, A. K., Hidalgo, J., Green, C. D., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.17.712502

Modélisation pathologique des maladies monogéniques par l'utilisation des cellules souches embryonnaires humaines : preuve de concept appliquée à la dystrophie myotonique de type 1

Denis, J. A. (2010) · theses.fr (ABES) · doi:10.70675/99903e3ezfc77z4fe6z870ez3fd60335eafa

The intestinal crypt, a prototype stem cell compartment

Clevers, H. (2013) · Cell · doi:10.1016/j.cell.2013.07.004 · Cited by 1,223

Stem cell self-renewal in intestinal crypt

Simons, B. D., & Clevers, H. C. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.07.010 · Cited by 154

The intestinal epithelial stem cell

Marshman, E., Booth, C., & Potten, C. S. (2002) · BioEssays · doi:10.1002/bies.10028 · Cited by 588

RESEARCH ARTICLE DEVELOPMENT AND STEM CELLS488

(2016)

Shifting paradigms in tissue stem cell biology: Insights from the intestine

Clevers, H. C. (2026) · Cell · doi:10.1016/j.cell.2025.12.025 · Cited by 29