Vertebrate Endoderm Development and Organ Formation

Wnt/β-Catenin Signaling in Development and Disease

Clevers, H. (2006) · Cell · doi:10.1016/j.cell.2006.10.018 · Cited by 5,568

Production of pancreatic hormone–expressing endocrine cells from human embryonic stem cells

D’Amour, K. A., Bang, A. G., Eliazer, S., Kelly, O., Agulnick, A. D., Smart, N. G., Moorman, M. A., KROON, E. J., Carpenter, M. K., & Baetge, E. E. (2006) · Nature Biotechnology · doi:10.1038/nbt1259 · Cited by 1,913

Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo

Kroon, E., Martinson, L. A., Kadoya, K., Bang, A. G., Kelly, O. G., Eliazer, S., Young, H., Richardson, M., Smart, N. G., Cunningham, J., et al. (2008) · Nature Biotechnology · doi:10.1038/nbt1393 · Cited by 1,843

Efficient differentiation of human embryonic stem cells to definitive endoderm

D'Amour, K. A., Agulnick, A. D., Eliazer, S., Kelly, O. G., Kroon, E., & Baetge, E. E. (2005) · Nature Biotechnology · doi:10.1038/nbt1163 · Cited by 1,730

Retinoic Acid Synthesis and Signaling during Early Organogenesis

Duester, G. (2008) · Cell · doi:10.1016/j.cell.2008.09.002 · Cited by 1,098

Development of definitive endoderm from embryonic stem cells in culture

Kubo, A., Shinozaki, K., Shannon, J. M., Kouskoff, V., Kennedy, M., Woo, S. L. C., Fehling, H. J., & Keller, G. M. (2004) · Development · doi:10.1242/dev.01044 · Cited by 830

Initiation of Mammalian Liver Development from Endoderm by Fibroblast Growth Factors

Jung, J., Zheng, M., Goldfarb, M., & Zaret, K. S. (1999) · Science · doi:10.1126/science.284.5422.1998 · Cited by 721

Depletion of definitive gut endoderm in Sox17 -null mutant mice

Kanai-Azuma, M., Kanai, Y., Gad, J. M., Tajima, Y., Taya, C., Kurohmaru, M., Sanai, Y., Yonekawa, H., Yazaki, K., Tam, P. P. L., et al. (2002) · Development · doi:10.1242/dev.129.10.2367 · Cited by 704

Origin and organization of the zebrafish fate map

Kimmel, C. B., Warga, R. M., & Schilling, T. F. (1990) · Development · doi:10.1242/dev.108.4.581 · Cited by 698

FGF Signaling Regulates Mesoderm Cell Fate Specification and Morphogenetic Movement at the Primitive Streak

Ciruna, B. G., & Rossant, J. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00017-x · Cited by 695

Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver

Gao, Y., Jin, Q., Gao, C., Chen, Y., Sun, Z., Guo, G., & Peng, J. (2022) · Cells · doi:10.3390/cells11203290 · Cited by 27

The TSP1-CD47-SIRPα interactome: an immune triangle for the checkpoint era

Montero, E., & Isenberg, J. S. (2023) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-023-03465-9 · Cited by 26

An Apo-14 Promoter-Driven Transgenic Zebrafish That Marks Liver Organogenesis

Wang, R., Li, Z., Wang, Y., & Gui, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022555 · Cited by 26

Differentiation into Endoderm Lineage: Pancreatic differentiation from Embryonic Stem Cells

Lee, D. H., & Chung, H. (2011) · International Journal of Stem Cells · doi:10.15283/ijsc.2011.4.1.35 · Cited by 26

Stem cells of the respiratory system: From identification to differentiation into functional epithelium

Green, M. D., Huang, S. X. L., & Snoeck, H. (2012) · BioEssays · doi:10.1002/bies.201200090 · Cited by 26

Enhancer Predictions and Genome-Wide Regulatory Circuits

Beer, M., Shigaki, D., & Huangfu, D. (2020) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-121719-010946 · Cited by 27

Dividing the Tubular Gut

Udager, A. M., Prakash, A., & Gumucio, D. L. (2010) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-381280-3.00002-6 · Cited by 26

CEA-induced PI3K/AKT pathway activation through the binding of CEA to KRT1 contributes to oxaliplatin resistance in gastric cancer

Chen, Y., Mi, Y., Tan, S., Chen, Y., Liu, S., Lin, S., Yang, C., Hong, W., & Li, W. (2024) · Drug Resistance Updates · doi:10.1016/j.drup.2024.101179 · Cited by 25

Distinct gene expression signatures in human embryonic stem cells differentiated towards definitive endoderm at single-cell level

Norrman, K., Strömbeck, A., Semb, H., & Ståhlberg, A. (2012) · Methods · doi:10.1016/j.ymeth.2012.03.030 · Cited by 25

Next-generation sequencing of NKX2.1 , FOXE1 , PAX8 , NKX2.5 , and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis

Wang, F., Liu, C., Jia, X., Liu, X., Xu, Y., Yan, S., Jia, X., Huang, Z., Liu, S., & Gu, M. (2017) · Clinica Chimica Acta · doi:10.1016/j.cca.2017.04.020 · Cited by 25

BMP signaling is required for nkx2.3-positive pharyngeal pouch progenitor specification in zebrafish

Li, L., Ning, G., Yang, S., Yan, Y., Cao, Y., & Wang, Q. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007996 · Cited by 24

Epigenetic factors Dnmt1 and Uhrf1 coordinate intestinal development

Ganz, J., Melançon, E., WILSON, C. A., Amores, A., Batzel, P., Strader, M. E., Braasch, I., Diba, P., Kuhlman, J. A., Postlethwait, J. H., et al. (2019) · Developmental Biology · doi:10.1016/j.ydbio.2019.08.002 · Cited by 24

Single-cell chromatin profiling of the primitive gut tube reveals regulatory dynamics underlying lineage fate decisions

Smith, R. J., Zhang, H., Hu, S. S., Yung, T. M., Francis, R., Lee, L., Onaitis, M. W., Dirks, P. B., Zang, C., & Kim, T.-H. (2022) · Nature Communications · doi:10.1038/s41467-022-30624-w · Cited by 24

Gene delivery in tissue engineering and regenerative medicine

Fang, Y. L., Chen, X., & Godbey, W. T. (2014) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.33354 · Cited by 24

Definitive Endoderm Formation from Plucked Human Hair-Derived Induced Pluripotent Stem Cells and SK Channel Regulation

Illing, A., Stockmann, M., Telugu, N. S., Linta, L., Russell, R., Müller, M., Seufferlein, T. T. W., Liebau, S., & Kleger, A. (2013) · Stem Cells International · doi:10.1155/2013/360573 · Cited by 24

Mouth development

Chen, J., Jacox, L. A., Saldanha, F. Y. L., & Sive, H. L. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.275 · Cited by 24

Identification of the central intermediate in the extra-embryonic to embryonic endoderm transition through single-cell transcriptomics

Rothová, M., Nielsen, A. V., Proks, M., Wong, Y. F., Riveiro, A. R., Linneberg-Agerholm, M., David, E., Amit, I., Trusina, A., & Brickman, J. M. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00923-x · Cited by 24

Pancreatic and Islet Development and Function: The Role of Thyroid Hormone.

Mastracci, T. L., & Evans‐Molina, C. (2014) · PubMed · Cited by 24

Development of the C. elegans digestive tract

Kormish, J. D., Gaudet, J., & McGhee, J. D. (2010) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.04.012 · Cited by 24

Anatomy and embryology of tracheo-esophageal fistula

Durkin, N., & Coppi, P. D. (2022) · Seminars in Pediatric Surgery · doi:10.1016/j.sempedsurg.2022.151231 · Cited by 23

Privileged portal metastasis of hepatocellular carcinoma in light of co-evolution of a visceral portal system and the liver in the chordate lineage: a search for therapeutic targets

Subbotin, V. M. (2018) · Drug Discovery Today · doi:10.1016/j.drudis.2018.01.020 · Cited by 23

Chemically-Defined, Xeno-Free, Scalable Production of hPSC-Derived Definitive Endoderm Aggregates with Multi-Lineage Differentiation Potential

Sahabian, A., Sgodda, M., Naujok, O., Dettmer, R., Dahlmann, J., Manstein, F., Cantz, T., Zweigerdt, R., Martin, U., & Olmer, R. (2019) · Cells · doi:10.3390/cells8121571 · Cited by 23

Endoderm-Derived Myeloid-like Metaphocytes in Zebrafish Gill Mediate Soluble Antigen-Induced Immunity

Lin, X., Zhou, Q., Lin, G., Zhao, C., & Wen, Z. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108227 · Cited by 23

Mesenchymal Niches for Digestive Organ Development, Homeostasis, and Disease

Loe, A. K. H., Rao‐Bhatia, A., Kim, J., & Kim, T.-H. (2020) · Trends in Cell Biology · doi:10.1016/j.tcb.2020.11.010 · Cited by 25

A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle

Yang, Y., Wang, H., He, J., Shi, W., Jiang, Z., Gao, L., Jiang, Y., Ni, R., Yang, Q., & Luo, L. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2025793118 · Cited by 23

Using Human Induced Pluripotent Stem Cell Derived Organoids to Identify New Pathologies in Patients with PDX1 Mutations

Krishnamurthy, M., Kechele, D. O., Broda, T. R., Zhang, X., Enriquez, J. R., McCauley, H. A., Sanchez, J. G., McCracken, K. W., Palermo, J., Bernieh, A., et al. (2021) · Gastroenterology · doi:10.1053/j.gastro.2022.06.083 · Cited by 23

Intestinal epithelial organoids: regeneration and maintenance of the intestinal epithelium

Oda, M., Hatano, Y., & Sato, T. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101977 · Cited by 24

Dual Inhibition of BMP and WNT Signals Promotes Pancreatic Differentiation from Human Pluripotent Stem Cells

Tan, M., Jiang, L., Li, Y., & Jiang, W. (2019) · Stem Cells International · doi:10.1155/2019/5026793 · Cited by 23

Reconstructing the pulmonary niche with stem cells: a lung story

Varghese, B., Ling, Z., & Ren, X. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02830-2 · Cited by 23

Developmental Molecular Biology of the Pancreas

Murtaugh, L. C., Cleaver, O. B., & MacDonald, R. J. (2018) · Springer eBooks · doi:10.1007/978-1-4939-7193-0_4 · Cited by 23

Retinoic Acid-Activated Ndrg1a Represses Wnt/β-catenin Signaling to Allow Xenopus Pancreas, Oesophagus, Stomach, and Duodenum Specification

Zhang, T., Guo, X., & Chen, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065058 · Cited by 23

Wnt/β-catenin signalling is necessary for gut differentiation in a marine annelid, Platynereis dumerilii

Žídek, R., Machoň, O., & Kozmík, Z. (2018) · EvoDevo · doi:10.1186/s13227-018-0100-7 · Cited by 23

Development of a 3D atlas of the embryonic pancreas for topological and quantitative analysis of heterologous cell interactions

Glorieux, L., Sapala, A., Willnow, D., Moulis, M., Salowka, A., Darrigrand, J.-F., Edri, S., Schonblum, A., Sakhneny, L., Schaumann, L., et al. (2022) · Development · doi:10.1242/dev.199655 · Cited by 22

Transplanted human intestinal organoids: a resource for modeling human intestinal development

Singh, A., Poling, H. M., Chaturvedi, P., Thorner, K., Sundaram, N., Kechele, D. O., Childs, C. J., McCauley, H. A., Fisher, G. W., Brown, N. E., et al. (2023) · Development · doi:10.1242/dev.201416 · Cited by 22

Retinoic acid is a key regulatory switch determining the difference between lung and thyroid fates in Xenopus laevis

Wang, J. H., Deimling, S. J., D'Alessandro, N. E., Zhao, L., Possmayer, F., & Drysdale, T. A. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-75 · Cited by 22

Ordered expression pattern of Hox and ParaHox genes along the alimentary canal in the ascidian juvenile

Nakayama, S., Satou, K., Orito, W., & Ogasawara, M. (2016) · Cell and Tissue Research · doi:10.1007/s00441-016-2360-7 · Cited by 22

Regulation of the Metal Transporters ZIP14 and ZnT10 by Manganese Intake in Mice

Felber, D. M., Wu, Y., & Zhao, N. (2019) · Nutrients · doi:10.3390/nu11092099 · Cited by 22

miR-335 promotes mesendodermal lineage segregation and shapes a transcription factor gradient in the endoderm

Yang, D., Lutter, D., Burtscher, I., Uetzmann, L., Theis, F. J., & Lickert, H. (2014) · Development · doi:10.1242/dev.104232 · Cited by 22

Metabolic regulation of intestinal homeostasis: molecular and cellular mechanisms and diseases

Zhang, R., Perekatt, A. O., & Chen, L. (2024) · MedComm · doi:10.1002/mco2.776 · Cited by 21

Sizzled-Tolloid Interactions Maintain Foregut Progenitors by Regulating Fibronectin-Dependent BMP Signaling

Kenny, A. P., Rankin, S. A., Allbee, A. W., Prewitt, A. R., Zhang, Z., Tabangin, M. E., Shifley, E. T., Louza, M. P., & Zorn, A. M. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.07.002 · Cited by 21

Potential for Pancreatic Maturation of Differentiating Human Embryonic Stem Cells Is Sensitive to the Specific Pathway of Definitive Endoderm Commitment

Jaramillo, M., Mathew, S., Task, K., Barner, S., & Banerjee, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094307 · Cited by 21

On the development of the hepatopancreatic ductal system

Villasenor, A., & Stainier, D. Y. R. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.02.003 · Cited by 21

Shaping development by stochasticity and dynamics in gene regulation

Dong, P., & Liu, Z. J. (2017) · Open Biology · doi:10.1098/rsob.170030 · Cited by 23

Differentiation of PTH-Expressing Cells From Human Pluripotent Stem Cells

Lawton, B. R., Martineau, C., Sosa, J. A., Roman, S. A., Gibson, C. E., Levine, M. A., & Krause, D. S. (2020) · Endocrinology · doi:10.1210/endocr/bqaa141 · Cited by 21

Derivation of Thyroid Follicular Cells From Pluripotent Stem Cells: Insights From Development and Implications for Regenerative Medicine

Posabella, A., Alber, A. B., Undeutsch, H. J., Droeser, R. A., Hollenberg, A. N., Ikonomou, L., & Kotton, D. N. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.666565 · Cited by 21

Digital reconstruction of full embryos during early mouse organogenesis

Xie, P., Shen, J., Yang, Y., Wang, X., Liu, W., Cao, H., Zheng, Y., Wu, C., Mao, G., He, J., et al. (2025) · Cell · doi:10.1016/j.cell.2025.05.035 · Cited by 21

Insight into Nephrocan Function in Mouse Endoderm Patterning

Addeo, M., Buonaiuto, S., Guerriero, I., Amendola, E., Visconte, F., Marino, A., Angelis, M. T. D., Russo, F., Roberto, L., Marotta, P., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010008 · Cited by 20

A dorsal-ventral gradient of Wnt3a/β-catenin signals controls mouse hindgut extension and colon formation

Garriock, R. J., Chalamalasetty, R. B., Zhu, J., Kennedy, M. W., Kumar, A., Mackem, S., & Yamaguchi, T. P. (2020) · Development · doi:10.1242/dev.185108 · Cited by 20

Centrioles Shape ERK Signaling Outcomes to Support Lung Branching

Xie, C., Abrams, S. R., Herranz‐Pérez, V., García‐Verdugo, J. M., & Reiter, J. F. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.11.020 · Cited by 20

Wnt-deficient and hypoxic environment orchestrates squamous reprogramming of human pancreatic ductal adenocarcinoma

Tamagawa, H., Fujii, M., Togasaki, K., Seino, T., Kawasaki, S., Takano, A., Toshimitsu, K., Takahashi, S., Ohta, Y., Matano, M., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01498-5 · Cited by 22

Spatiotemporal and genetic cell lineage tracing of endodermal organogenesis at single-cell resolution

Li, K., Yu, P.-L., Zheng, Q.-Q., Wang, X., Fang, X., Li, L., & Xu, C. (2025) · Cell · doi:10.1016/j.cell.2024.12.012 · Cited by 20

An essential role for heat shock transcription factor binding protein 1 (HSBP1) during early embryonic development

Eroglu, B., Min, J., Zhang, Y., Szurek, E. A., Moskophidis, D., Eroğlu, A., & Mivechi, N. F. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2013.12.038 · Cited by 20

Differential response of epiblast stem cells to Nodal and Activin signalling: a paradigm of early endoderm development in the embryo

Kaufman‐Francis, K., Goh, H. N., Kojima, Y., Studdert, J. B., Jones, V. J., Power, M., Wilkie, E. E., Teber, E., Loebel, D. A. F., & Tam, P. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0550 · Cited by 20

Antero-posterior ectoderm patterning by canonical Wnt signaling during ascidian development

Feinberg, S. L., Roure, A., Piron, J., & Darras, S. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008054 · Cited by 20

Expression of Piwi, MMP, TIMP, and Sox during Gut Regeneration in Holothurian Eupentacta fraudatrix (Holothuroidea, Dendrochirotida)

Dolmatov, I. Y., Kalacheva, N. V., Tkacheva, E. S., Shulga, A. P., Zavalnaya, E. G., Shamshurina, E. V., Girich, A. S., Boyko, A. V., & Елисейкина, М. Г. (2021) · Genes · doi:10.3390/genes12081292 · Cited by 20

Applied Developmental Biology

Melton, D. A. (2016) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2015.11.013 · Cited by 19

Xenogeneic-Free Human Intestinal Organoids for Assessing Intestinal Nutrient Absorption

Inoue, M., Tanaka, Y., Matsushita, S., Shimozaki, Y., Ayame, H., & Akutsu, H. (2022) · Nutrients · doi:10.3390/nu14030438 · Cited by 19

The Multi-Omics Analysis Revealed a Metabolic Regulatory System of Cecum in Rabbit with Diarrhea

Wang, J., Zhao, K., Kang, Z., Wang, M., Yang, C., Fan, H., Xia, S., & Lai, S. (2022) · Animals · doi:10.3390/ani12091194 · Cited by 19

In silico discovery of small molecules for efficient stem cell differentiation into definitive endoderm

Novakovsky, G., Sasaki, S., Fornés, O., Omur, M. E., Huang, H., Bayly, C. L., Zhang, D., Lim, N., Cherkasov, A. R., Pavlidis, P., et al. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.01.008 · Cited by 21

Generating cells of the gastrointestinal system: current approaches and applications for the differentiation of human pluripotent stem cells

Wang, A., & Sander, M. (2012) · Journal of Molecular Medicine · doi:10.1007/s00109-012-0923-y · Cited by 19

Inter-organ regulation of Drosophila intestinal stem cell proliferation by a hybrid organ boundary zone

Sawyer, J. K., Cohen, E., & Fox, D. T. (2017) · Development · doi:10.1242/dev.153114 · Cited by 19

Functional Enterospheres Derived In Vitro from Human Pluripotent Stem Cells

Nadkarni, R. R., Abed, S., Cox, B., Bhatia, S., Lau, J. T., Surette, M. G., & Draper, J. S. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.07.024 · Cited by 19

Endodermal pouch-expressed dmrt2b is important for pharyngeal cartilage formation

Li, L., Mao, A., Wang, P., Ning, G., Cao, Y., & Wang, Q. (2018) · Biology Open · doi:10.1242/bio.035444 · Cited by 19

Signals and forces shaping organogenesis of the small intestine

Wang, S., Walton, K. D., & Gumucio, D. L. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2018.12.001 · Cited by 19

Mechanobiology of vertebrate gut morphogenesis

Durel, J. F., & Nerurkar, N. L. (2020) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.04.002 · Cited by 20

An Efficient Method for the Differentiation of Human iPSC-Derived Endoderm toward Enterocytes and Hepatocytes

Qiu, S., Li, Y., Imakura, Y., Mima, S., Hashita, T., Iwao, T., & Matsunaga, T. (2021) · Cells · doi:10.3390/cells10040812 · Cited by 19

Time Course Transcriptomic Study Reveals the Gene Regulation During Liver Development and the Correlation With Abdominal Fat Weight in Chicken

Xing, S., Liu, R., Zhao, G., Groenen, M. A. M., Madsen, O., Liu, L., Zheng, M., Wang, Q., Wu, Z., Crooijmans, R. P. M. A., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.723519 · Cited by 19

Frogs as integrative models for understanding digestive organ development and evolution

Womble, M. A., Pickett, M. A., & Nascone‐Yoder, N. M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.02.001 · Cited by 19

What gastroenterologists and hepatologists should know about organoids in 2019

Günther, C., Brevini, T., Sampaziotis, F., & Neurath, M. F. (2019) · Digestive and Liver Disease · doi:10.1016/j.dld.2019.02.020 · Cited by 20

Stem cell-based multi-tissue platforms to model human autoimmune diabetes

Leavens, K. F., Alvarez‐Dominguez, J. R., Vo, L. T., Russ, H. A., & Parent, A. V. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101610 · Cited by 18

Islets in the body are never flat: transitioning from two-dimensional (2D) monolayer culture to three-dimensional (3D) spheroid for better efficiency in the generation of functional hPSC-derived pancreatic β cells in vitro

Diané, A., Mohammed, L. I., & Al-Siddiqi, H. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01171-8 · Cited by 20

Connexin 43 is involved in early differentiation of human embryonic stem cells

Peng, Q., Yue, C., Chen, A. C. H., Lee, K. C., Fong, S. W., Yeung, W. S. B., & Lee, Y. L. (2018) · Differentiation · doi:10.1016/j.diff.2018.12.003 · Cited by 18

Generation of Human Stomach Cancer iPSC-Derived Organoids Induced by Helicobacter pylori Infection and Their Application to Gastric Cancer Research

Ku, C., Wuputra, K., Pan, J.-B., Li, C.-P., Liu, C., Liu, Y., Saito, S., Chan, T., Lin, C., Wu, D., et al. (2022) · Cells · doi:10.3390/cells11020184 · Cited by 18

Uncovering the mesendoderm gene regulatory network through multi-omic data integration

Jansen, C. S., Paraiso, K. D., Zhou, J. J., Blitz, I. L., Fish, M. B., Charney, R. M., Cho, J. S., Yasuoka, Y., Sudou, N., Bright, A. R., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110364 · Cited by 18

Endoderm-derived islet1-expressing cells differentiate into endothelial cells to function as the vascular HSPC niche in zebrafish

Nakajima, H., Ishikawa, H., Yamamoto, T., Chiba, A., Fukui, H., Sako, K., Fukumoto, M., Mattonet, K., Kwon, H.-B., Hui, S. P., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2022.12.013 · Cited by 18

Enhancer decommissioning by Snail1-induced competitive displacement of TCF7L2 and down-regulation of transcriptional activators results in EPHB2 silencing

Schnappauf, O., Beyes, S., Dertmann, A., Freihen, V., Frey, P., Jägle, S., Rose, K., Michoel, T., Grosschedl, R., & Hecht, A. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.08.002 · Cited by 18

Differentiation of human airway-organoids from induced pluripotent stem cells (iPSCs)

Wang, R., McCauley, K. B., Kotton, D. N., & Hawkins, F. J. (2020) · Methods in cell biology · doi:10.1016/bs.mcb.2020.03.008 · Cited by 18

Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells

Mukherjee, S., French, D. L., & Gadue, P. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.09.004 · Cited by 17

Stem Cells in Regenerative Medicine: A Journey from Adult Stem Cells to Induced Pluripotent Cells

Rocca, Y. D., Mazzone, A., Marconi, G. D., Trubiani, O., Pizzicannella, J., & Diomede, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178255 · Cited by 19

Loss of mesenchymal bone morphogenetic protein signaling leads to development of reactive stroma and initiation of the gastric neoplastic cascade

Roy, S. A. B., Allaire, J. M., Ouellet, C., Maloum-Rami, F., Pomerleau, V., Lemieux, É., Babeu, J., Rousseau, J., Paquet, M., Garde‐Granger, P., et al. (2016) · Scientific Reports · doi:10.1038/srep32759 · Cited by 17

Species-Specific Rewiring of Definitive Endoderm Developmental Gene Activation via Endogenous Retroviruses Through TET1 Mediated Demethylation

Wu, F., Liufu, Z., Liu, Y., Guo, L., Wu, J., Cao, S., Qin, Y., Guo, N., Fu, Y., Liu, H., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111791 · Cited by 17

A BAC transgenic Hes1-EGFP reporter reveals novel expression domains in mouse embryos

Klinck, R., Füchtbauer, E., Ahnfelt‐Rønne, J., Serup, P., Jensen, J. N., & Jørgensen, M. C. (2011) · Gene Expression Patterns · doi:10.1016/j.gep.2011.06.004 · Cited by 17

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