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

Bronchiolar Progenitor Cells

Chen, H., Matsumoto, K., & Stripp, B. R. (2009) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200907-078rm · Cited by 24

Intestinal stem cells and intestinal organoids

Zhao, Q., Guan, J., & Wang, X. (2020) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2020.06.005 · Cited by 23

Role of microbiota and related metabolites in gastrointestinal tract barrier function in NAFLD

Fernández-Cantos, M. V., García-Morena, D., Iannone, V., El-Nezami, H. S., Kolehmainen, M., & Kuipers, O. P. (2021) · Tissue Barriers · doi:10.1080/21688370.2021.1879719 · Cited by 23

Activation of G protein coupled estrogen receptor prevents chemotherapy-induced intestinal mucositis by inhibiting the DNA damage in crypt cell in an extracellular signal-regulated kinase 1- and 2- dependent manner

Chen, G., Zeng, H., Li, X., Liu, J., Zhao, L., Xu, R., Ma, Y., Liu, C., & Xue, B. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04325-z · Cited by 24

Lysozyme-rich mucus metaplasia in duodenal crypts supersedes Paneth cells in celiac disease

Rubio‐Terres, C. (2011) · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · doi:10.1007/s00428-011-1129-3 · Cited by 23

Beta-catenin/TCF4 transactivates miR-30e during intestinal cell differentiation

Liao, Y., & Lönnerdal, B. L. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0366-y · Cited by 23

Transcriptional corepressor MTG16 regulates small intestinal crypt proliferation and crypt regeneration after radiation-induced injury

Poindexter, S. V., Reddy, V. K., Mittal, M. K., Williams, A. M., Washington, M. K., Harris, E. I., Mah, A. T., Hiebert, S. W., Singh, K., Chaturvedi, R., et al. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00253.2014 · Cited by 23

Abnormalities in ileal stem, neurogenin 3, and enteroendocrine cells in patients with irritable bowel syndrome

El‐Salhy, M., & Gilja, O. H. (2017) · BMC Gastroenterology · doi:10.1186/s12876-017-0643-4 · Cited by 23

Effect of diet and individual dietary guidance on gastrointestinal endocrine cells in patients with irritable bowel syndrome (Review)

Mazzawi, T. R. E., & El‐Salhy, M. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3096 · Cited by 23

The POU/Oct Transcription Factor Nubbin Controls the Balance of Intestinal Stem Cell Maintenance and Differentiation by Isoform-Specific Regulation

Tang, X., Zhao, Y., Buchon, N., & Engström, Y. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.03.014 · Cited by 24

Formation of arrays of planar, murine, intestinal crypts possessing a stem/proliferative cell compartment and differentiated cell zone

Kim, R., Wang, Y., Hwang, S.-H. J., Attayek, P. J., Smiddy, N. M., Reed, M. I., Sims, C. E., & Allbritton, N. L. (2018) · Lab on a Chip · doi:10.1039/c8lc00332g · Cited by 23

Nkx2.2 is expressed in a subset of enteroendocrine cells with expanded lineage potential

Groß, S., Balderes, D. A., Liu, J., Asfaha, S., Gu, G., Wang, T. C., & Sussel, L. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00244.2015 · Cited by 22

The intestinal epithelial response to damage

Weichselbaum, L., & Klein, O. D. (2018) · Science China Life Sciences · doi:10.1007/s11427-018-9331-y · Cited by 22

Tissue-specific reduction in MLH1 expression induces microsatellite instability in intestine of Mlh1 mice

Shrestha, K. S., Aska, E.-M., Tuominen, M. M., & Kauppi, L. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103178 · Cited by 22

NF-κB determines Paneth versus goblet cell fate decision in the small intestine

Brischetto, C., Krieger, K., Klotz, C., Krahn, I., Kunz, S., Kolesnichenko, M., Mucka, P., Heuberger, J., Scheidereit, C., & Schmidt‐Ullrich, R. (2021) · Development · doi:10.1242/dev.199683 · Cited by 25

Inflammatory cues acting on the adult intestinal stem cells and the early onset of cancer (Review)

Barbaro, A. D. L., Perletti, G., Bonapace, I. M., & Monti, E. (2014) · International Journal of Oncology · doi:10.3892/ijo.2014.2490 · Cited by 22

Dysregulation of laminins in intestinal inflammation

Spenlé, C., Hussenet, T., Lacroute, J., Lefèbvre, O., Kédinger, M., Orend, G., & Simon-Assmann, P. M. (2011) · Pathologie Biologie · doi:10.1016/j.patbio.2011.10.005 · Cited by 22

Mixed Adenoneuroendocrine Carcinoma, Amphicrine Type, of the Small Bowel

Ludmir, E. B., McCall, S. J., Cardona, D. M., Perkinson, K. R., Guy, C. D., & Zhang, X. (2016) · American Journal of Clinical Pathology · doi:10.1093/ajcp/aqw028 · Cited by 22

Mapping mammary gland architecture using multi-scale in situ analysis

Fernández‐González, R., Illa-Bochaca, I., Welm, B. E., Fleisch, M. C., Werb, Z., Ortíz-de-Solórzano, C., & Barcellos‐Hoff, M. H. (2008) · Integrative Biology · doi:10.1039/b816933k · Cited by 24

Wnt/β-catenin Signaling Inhibitors suppress the Tumor-initiating properties of a CD44 + CD133 + subpopulation of Caco-2 cells

Kim, J., Choi, K.-W., Lee, J., Lee, J., Lee, S., Sun, R., & Kim, J. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.58612 · Cited by 21

H3K36 methylation regulates cell plasticity and regeneration in the intestinal epithelium

Swearingen, A. R., Meyer, A. R., Bussey-Sutton, C. R., O’Connor, E. S., Coradin, M., Coulombe, M., Riemondy, K. A., Potlapelly, S., Strahl, B. D., Hansson, G. C., et al. (2025) · Nature Cell Biology · doi:10.1038/s41556-024-01580-y · Cited by 23

Is adult stem cell aging driven by conflicting modes of chromatin remodeling?

Przybilla, J., Galle, J., & Rohlf, T. (2012) · BioEssays · doi:10.1002/bies.201100190 · Cited by 21

Short-range cytokine gradients to mimic paracrine cell interactions in vitro

Ansorge, M., Rastig, N., Steinborn, R., König, T., Baumann, L., Möller, S., Schnabelrauch, M., Cross, M. A., Werner, C., Beck‐Sickinger, A. G., et al. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.12.053 · Cited by 21

Dietary Copper Improves Intestinal Morphology via Modulating Intestinal Stem Cell Activity in Pigs

Yin, L., Yang, Q., Zhang, Y., Wan, D., Yin, Y., Wang, Q., Huang, J., Li, J., Yang, H., & Yin, Y. (2021) · Animals · doi:10.3390/ani11092513 · Cited by 21

Crosstalk Between Intestinal Microbiota Derived Metabolites and Tissues in Allogeneic Hematopoietic Cell Transplantation

Fujiwara, H. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.703298 · Cited by 22

In vitro impact of amino acid-derived bacterial metabolites on colonocyte mitochondrial activity, oxidative stress response and DNA integrity

Armand, L., Andriamihaja, M., Gellenoncourt, S., Bitane, V., Lan, A., & Blachier, F. (2019) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2019.04.018 · Cited by 21

TLR4 Agonist Monophosphoryl Lipid A Alleviated Radiation-Induced Intestinal Injury

Guo, J., Liu, Z., Zhang, D., Chen, Y., Qin, H., Liu, T., Liu, C., Cui, J., Li, B., Yang, Y., et al. (2019) · Journal of Immunology Research · doi:10.1155/2019/2121095 · Cited by 21

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) · Genome biology · doi:10.1186/s13059-020-01976-7 · Cited by 22

The Cell Cycle

Yang, V. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809954-4.00008-6 · Cited by 24

Purpose and regulation of stem cells: a systems‐biology view from the Caenorhabditis elegans germ line

Cinquin, O. (2008) · The Journal of Pathology · doi:10.1002/path.2481 · Cited by 21

Brain Organoids: Expanding Our Understanding of Human Development and Disease

Chuye, L. E. B., Dimitri, A. J., Desai, A., Handelmann, C. R., Bae, Y., Johari, P., Jornet, J. M., Klejbor, I., Stachowiak, M. K., & Stachowiak, E. K. (2018) · Results and problems in cell differentiation · doi:10.1007/978-3-319-93485-3_8 · Cited by 20

Vitamin D3 suppresses intestinal epithelial stemness via ER stress induction in intestinal organoids

Sittipo, P., Kim, K., Han, J., Lee, M. R., & Lee, Y. K. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02361-2 · Cited by 20

Guanylyl cyclase 2C (GUCY2C) in gastrointestinal cancers: recent innovations and therapeutic potential

Entezari, A. A., Snook, A. E., & Waldman, S. A. (2021) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2021.1937124 · Cited by 20

A LGR5 reporter pig model closely resembles human intestine for improved study of stem cells in disease

Schaaf, C. R., Polkoff, K. M., Carter, A., Stewart, A. S., Sheahan, B. J., Freund, J. M., Ginzel, J. D., Snyder, J. C., Roper, J., Piedrahita, J. A., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202300223r · Cited by 20

Host–diet–microbiota interplay in intestinal nutrition and health

Ignatiou, A., & Pitsouli, C. (2024) · FEBS Letters · doi:10.1002/1873-3468.14966 · Cited by 21

Obesity and intestinal stem cell susceptibility to carcinogenesis

Pourvali, K., & Monji, H. (2021) · Nutrition & Metabolism · doi:10.1186/s12986-021-00567-y · Cited by 22

NOD2 Supports Crypt Survival and Epithelial Regeneration after Radiation-Induced Injury

Lee, C., Choi, C., Kang, H. S., Shin, S.-W., Kim, S., Park, H. C., & Hong, S. N. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174297 · Cited by 20

Porcine colonoids and enteroids keep the memory of their origin during regeneration

Barnett, A. M., Mullaney, J. A., Hendriks, C., Borgne, L. L., McNabb, W. C., & Roy, N. C. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00420.2020 · Cited by 19

Biomaterials and bioengineering to guide tissue morphogenesis in epithelial organoids

Jeon, E. Y., Sorrells, L., & Abaci, H. E. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.1038277 · Cited by 20

An Insight on Microfluidic Organ-on-a-Chip Models for PM2.5-Induced Pulmonary Complications

Shah, D., Dave, B. P., Chorawala, M. R., Prajapati, B. G., Singh, S. K., Elossaily, G. M., Ansari, M. N., & Ali, N. (2024) · ACS Omega · doi:10.1021/acsomega.3c10271 · Cited by 19

The role of cell location and spatial gradients in the evolutionary dynamics of colon and intestinal crypts

Shahriyari, L., Komarova, N. L., & Jilkine, A. (2016) · Biology Direct · doi:10.1186/s13062-016-0141-6 · Cited by 19

A microRNA-mRNA expression network during oral siphon regeneration in Ciona

Spina, E. J., Guzman, E., Zhou, H., Kosik, K. S., & Smith, W. C. (2017) · Development · doi:10.1242/dev.144097 · Cited by 19

Different RNA and protein expression of surface markers in rabbit amniotic fluid‐derived mesenchymal stem cells

Kováč, M., Vašíček, J., Kulíková, B., Bauer, M., Čurlej, J., Baláži, A., & Chrenek, P. (2017) · Biotechnology Progress · doi:10.1002/btpr.2519 · Cited by 19

Intestinal Stem Cell Development in the Neonatal Gut: Pathways Regulating Development and Relevance to Necrotizing Enterocolitis

Venkatraman, A., Yu, W., Nitkin, C. R., & Sampath, V. (2021) · Cells · doi:10.3390/cells10020312 · Cited by 19

Neural Stem Cell Regulation in Zebrafish

Foley, T., Thétiot, M., & Bally‐Cuif, L. (2024) · Annual Review of Genetics · doi:10.1146/annurev-genet-111523-101949 · Cited by 18

Metabolic Interaction Between Host and the Gut Microbiota During High-Fat Diet-Induced Colorectal Cancer

Lee, C., Lee, S., & Yoo, W. (2024) · The Journal of Microbiology · doi:10.1007/s12275-024-00123-2 · Cited by 20

Recent advances in the diagnosis of irritable bowel syndrome

El‐Salhy, M. (2015) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/17474124.2015.1067138 · Cited by 18

Cell shape and TGF‐β signaling define the choice of lineage during in vitro differentiation of mouse primary hepatic precursors

Akkari, L., Haouzi, D., Binamé, F., Floc’h, N., Lassus, P., Baghdiguian, S., & Hibner, U. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22219 · Cited by 19

Investigating the Relation between Stochastic Differentiation, Homeostasis and Clonal Expansion in Intestinal Crypts via Multiscale Modeling

Graudenzi, A., Caravagna, G., Matteis, G. D., & Antoniotti, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097272 · Cited by 18

Engineering the Future of Regenerative Medicines in Gut Health with Stem Cell-Derived Intestinal Organoids

Kumar, D., Gupta, S., Gupta, V., Tanwar, R., & Chandel, A. (2025) · Stem Cell Reviews and Reports · doi:10.1007/s12015-025-10893-w · Cited by 18

Inactivation of Interferon Regulatory Factor 1 Causes Susceptibility to Colitis-Associated Colorectal Cancer

Jeyakumar, T., Fodil, N., Kraak, L. V. D., Meunier, C., Cayrol, R., McGregor, K., Langlais, D., Greenwood, C. M. T., Beauchemin, N., & Gros, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-55378-2 · Cited by 17

The duration of food withdrawal affects the intestinal structure, nutrients absorption, and utilization in broiler chicken

Wang, Y., Wu, Y., Chen, J., Guo, X., Yan, L., Guo, Y., Wang, B., & Yuan, J. (2020) · The FASEB Journal · doi:10.1096/fj.202001773r · Cited by 17

Segmentation of human functional tissue units in support of a Human Reference Atlas

Jain, Y., Godwin, L. L., Ju, Y., Sood, N., Quardokus, E. M., Bueckle, A., Longacre, T. A., Horning, A. M., Lin, Y., Esplin, E. D., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-04848-5 · Cited by 21

Gastric epithelial stem cells in development, homeostasis and regeneration

Alvina, F. B., Chen, T. C.-Y., Lim, H. Y. G., & Barker, N. (2023) · Development · doi:10.1242/dev.201494 · Cited by 17

Cell Cycle Heterogeneity in the Small Intestinal Crypt and Maintenance of Genome Integrity

Pruitt, S. C., Freeland, A. L., & Kudla, A. (2010) · Stem Cells · doi:10.1002/stem.450 · Cited by 17

Cyclic nucleotide signaling in intestinal epithelia: getting to the gut of the matter

Arshad, N., & Visweswariah, S. S. (2013) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1223 · Cited by 17

Cited1 Deficiency Suppresses Intestinal Tumorigenesis

Méniel, V. S., Song, F., Phesse, T. J., Young, M. A., Poetz, O., Parry, L., Jenkins, J. R., Williams, G. T., Dunwoodie, S. L., Watson, A. J. M., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003638 · Cited by 17

Pharmacokinetics and Toxicity in Rats and Monkeys of coDbait: A Therapeutic Double-stranded DNA Oligonucleotide Conjugated to Cholesterol

Schlegel, A., Buhler, C., Devun, F., Agrario, C., Urien, S., Lokiec, F. M., Sun, J., & Dutreix, M. (2012) · Molecular Therapy — Nucleic Acids · doi:10.1038/mtna.2012.27 · Cited by 20

Chimeric mice reveal clonal development of pancreatic acini, but not islets

Swenson, E. S., Xanthopoulos, J. M., Nottoli, T., McGrath, J. M., Theise, N. D., & Krause, D. S. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.104 · Cited by 16

Recent advances in understanding intestinal stem cell regulation

Hu, D., Yan, H., He, X., & Li, L. (2019) · F1000Research · doi:10.12688/f1000research.16793.1 · Cited by 16

Effect of trehalose supplementation on growth performance and intestinal morphology in broiler chickens

Ruangpanit, Y., Matsushita, K., Mukai, K., & Kikusato, M. (2020) · Veterinary and Animal Science · doi:10.1016/j.vas.2020.100142 · Cited by 16

Ochratoxin A at nanomolar concentration perturbs the homeostasis of neural stem cells in highly differentiated but not in immature three-dimensional brain cell cultures

Zurich, M., & Honegger, P. (2011) · Toxicology Letters · doi:10.1016/j.toxlet.2011.06.007 · Cited by 16

Effect of abrasive properties of sedges on intestinal absorptive surface and Resting Metabolic Rate of the root voles

Wieczorek, M., Szafrańska, P. A., Łabęcka, A. M., Lázaro, J., & Konarzewski, M. (2014) · Journal of Experimental Biology · doi:10.1242/jeb.117168 · Cited by 16

Human intestinal organoids from Cronkhite-Canada syndrome patients reveal link between serotonin and proliferation

Poplaski, V. B., Bomidi, C., Kambal, A., Nguyen‐Phuc, H., Rienzi, S. C. D., Danhof, H. A., Zeng, X.-L., Feagins, L. A., Deng, N., Vilar, E., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci166884 · Cited by 15

Intestinal stem cells and stem cell-based therapy for intestinal diseases

Mohamed, M. S., Chen, Y., & Yao, C. (2014) · Cytotechnology · doi:10.1007/s10616-014-9753-9 · Cited by 15

Molecular pathways driving disease-specific alterations of intestinal epithelial cells

López-Posadas, R., Neurath, M. F., & Atreya, I. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2363-2 · Cited by 16

Regenerative medicine for the upper gastrointestinal tract

Kanetaka, K., & Eguchi, S. (2020) · Regenerative Therapy · doi:10.1016/j.reth.2020.07.002 · Cited by 15

A diarylpentanoid curcumin analog exhibits improved radioprotective potential in the intestinal mucosa

Fukuda, K., Uehara, Y., Nakata, E., Inoue, M., Shimazu, K., Yoshida, T., Kanda, H., Nanjo, H., Hosoi, Y., Yamakoshi, H., et al. (2016) · International Journal of Radiation Biology · doi:10.3109/09553002.2016.1164910 · Cited by 15

Indispensable role of Notch ligand-dependent signaling in the proliferation and stem cell niche maintenance of APC-deficient intestinal tumors

Nakata, T., Shimizu, H., Nagata, S., Ito, G., Fujii, S., Suzuki, K., Kawamoto, A., Ishibashi, F., Kuno, R., Anzai, S., et al. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.12.031 · Cited by 15

Variations in the management of diarrhoea induced by cancer therapy: results from an international, cross-sectional survey among European oncologists

Kordes, M., & Gerling, M. (2019) · ESMO Open · doi:10.1136/esmoopen-2019-000607 · Cited by 15

Intestinal stem cells – types and markers

Zhang, Z., & Huang, J. (2013) · Cell Biology International · doi:10.1002/cbin.10049 · Cited by 15

The drug monosodium luminol (GVT) preserves crypt-villus epithelial organization and allows survival of intestinal T cells in mice infected with the ts1 retrovirus

Scofield, V. L., Yan, M., Kuang, X., Kim, S., & Wong, P. K. Y. (2009) · Immunology Letters · doi:10.1016/j.imlet.2008.12.012 · Cited by 15

Secretagogues stimulate electrogenic HCO3–secretion in the ileum of the brushtail possum,Trichosurus vulpecula:evidence for the role of a Na+/HCO3– cotransporter

Bartolo, R. C., Harfoot, N., Gill, M., McLeod, B. J., & Butt, G. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.028928 · Cited by 15

Enteroendocrine cells, stem cells and differentiation progenitors in rats with TNBS-induced colitis

El‐Salhy, M., Mazzawi, T. R. E., Umezawa, K., & Gilja, O. H. (2016) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2016.2787 · Cited by 15

Cell clusters containing intestinal stem cells, line the zebrafish intestine intervillus pocket

Tavakoli, S., Zhu, S., & Matsudaira, P. T. (2022) · iScience · doi:10.1016/j.isci.2022.104280 · Cited by 14

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) · Cell Communication and Signaling · doi:10.1186/s12964-023-01140-1 · Cited by 14

Possible role of intestinal stem cells in the pathophysiology of irritable bowel syndrome

El‐Salhy, M. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i13.1427 · Cited by 15

Radiobiological Modifiers in Clinical Radiation Oncology: Current Reality and Future Potential

Allison, R. R. (2014) · Future Oncology · doi:10.2217/fon.14.174 · Cited by 14

Size effect and mucus role on the intestinal toxicity of the E551 food additive and engineered silica nanoparticles

Zaiter, T., Cornu, R., Millot, N., Herbst-Ghysel, M., Pellequer, Y., Moarbess, G., Martin, H., Diab‐Assaf, M., & Béduneau, A. (2022) · Nanotoxicology · doi:10.1080/17435390.2022.2063084 · Cited by 14

A simple, cost-effective and flexible method for processing of snap-frozen tissue to prepare large amounts of intact RNA using laser microdissection

Grover, P. K., Cummins, A. G., Price, T. J., Roberts‐Thomson, I. C., & Hardingham, J. E. (2012) · Biochimie · doi:10.1016/j.biochi.2012.06.031 · Cited by 13

Role of Ldb1 in Adult Intestinal Homeostasis

Dey‐Guha, I., Mukhopadhyay, M., Phillips, M., & Westphal, H. (2009) · International Journal of Biological Sciences · doi:10.7150/ijbs.5.686 · Cited by 13

Oral drugs against COVID-19

Mikus, G., Foerster, K. I., Terstegen, T., Vogt, C. J., Said, A., Schulz, M., & Haefeli, W. E. (2022) · Deutsches Ärzteblatt international · doi:10.3238/arztebl.m2022.0152 · Cited by 13

PKH26 Staining Defines Distinct Subsets of Normal Human Colon Epithelial Cells at Different Maturation Stages

Pastò, A., Marchesi, M., Diamantini, A., Frasson, C., Curtarello, M., Lago, C., Pilotto, G., Parenti, A. R., Esposito, G., Agostini, M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043379 · Cited by 13

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RESEARCH ARTICLE DEVELOPMENT AND STEM CELLS488

(2016)

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