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Items: 1 to 20 of 80

1.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
AbstractArticlePDF–4.8M
2.
Cripto Is Targeted by miR-1a-3p in a Mouse Model of Heart Development
Tiziana Angrisano, Francesca Varrone, Elvira Ragozzino, Annalisa Fico, Gabriella Minchiotti, Mariarita Brancaccio
Int J Mol Sci. 2023 Aug; 24(15): 12251. Published online 2023 Jul 31. doi: 10.3390/ijms241512251
PMCID:
PMC10419258
AbstractArticlePDF–4.4M
3.
Spatiotemporal transcriptomic maps of whole mouse embryos at the onset of organogenesis
Abhishek Sampath Kumar, Luyi Tian, Adriano Bolondi, Amèlia Aragonés Hernández, Robert Stickels, Helene Kretzmer, Evan Murray, Lars Wittler, Maria Walther, Gabriel Barakat, Leah Haut, Yechiel Elkabetz, Evan Z. Macosko, Léo Guignard, Fei Chen, Alexander Meissner
Nat Genet. 2023; 55(7): 1176–1185. Published online 2023 Jul 6. doi: 10.1038/s41588-023-01435-6
PMCID:
PMC10335937
AbstractArticlePDF–25M
4.
A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Alexis Leigh Krup, Sarah A. B. Winchester, Sanjeev S. Ranade, Ayushi Agrawal, W. Patrick Devine, Tanvi Sinha, Krishna Choudhary, Martin H. Dominguez, Reuben Thomas, Brian L. Black, Deepak Srivastava, Benoit G. Bruneau
Development. 2023 May 1; 150(9): dev201229. Published online 2023 May 2. doi: 10.1242/dev.201229
PMCID:
PMC10259516
AbstractArticle
5.
Cripto favors chondrocyte hypertrophy via TGF‐β SMAD1/5 signaling during development of osteoarthritis
Amaya Garcia de Vinuesa, Gonzalo Sanchez‐Duffhues, Esmeralda Blaney‐Davidson, Arjan van Caam, Kirsten Lodder, Yolande Ramos, Margreet Kloppenburg, Ingrid Meulenbelt, Peter van der Kraan, Marie‐José Goumans, Peter ten Dijke
J Pathol. 2021 Nov; 255(3): 330–342. Published online 2021 Sep 6. doi: 10.1002/path.5774
PMCID:
PMC9292799
AbstractArticlePDF–20M
6.
NANOG initiates epiblast fate through the coordination of pluripotency genes expression
Nicolas Allègre, Sabine Chauveau, Cynthia Dennis, Yoan Renaud, Dimitri Meistermann, Lorena Valverde Estrella, Pierre Pouchin, Michel Cohen-Tannoudji, Laurent David, Claire Chazaud
Nat Commun. 2022; 13: 3550. Published online 2022 Jun 21. doi: 10.1038/s41467-022-30858-8
PMCID:
PMC9213552
AbstractArticlePDF–4.4M
7.
Oncofetal Protein CRIPTO Is Involved in Wound Healing and Fibrogenesis in the Regenerating Liver and Is Associated with the Initial Stages of Cardiac Fibrosis
Sofia Karkampouna, Danny van der Helm, Mario Scarpa, Bart van Hoek, Hein W. Verspaget, Marie-Jose Goumans, Minneke J. Coenraad, Boudewijn P.T. Kruithof, Marianna Kruithof-de Julio
Cells. 2021 Dec; 10(12): 3325. Published online 2021 Nov 26. doi: 10.3390/cells10123325
PMCID:
PMC8699799
AbstractArticlePDF–6.1M
8.
Liver-specific over-expression of Cripto-1 in transgenic mice promotes hepatocyte proliferation and deregulated expression of hepatocarcinogenesis-related genes and signaling pathways
Yu Liu, Yan-Qing Li, Shi-Hao Huang, Yong-Long Li, Jia-Wei Xia, Jun-Shuang Jia, Fang Wei, Jia-Hong Wang, Guan-Qi Dai, Yu-Cai Wang, Xiao-Yan Li, Liu-Xin Han, Xiao-Ling Zhang, Xu-Dong Xiang, Wen-Tao Zhao, Dong Xiao, Xiao-Lin Lin
Aging (Albany NY) 2021 Sep 15; 13(17): 21155–21190. Published online 2021 Sep 13. doi: 10.18632/aging.203402
PMCID:
PMC8457585
AbstractArticlePDF–3.3M
9.
Maternal Cripto is required for proper uterine decidualization and peri-implantation uterine remodeling
Shiva Shafiei, Omar Farah, Daniel Dufort
Biol Reprod. 2021 May; 104(5): 1045–1057. Published online 2021 Feb 16. doi: 10.1093/biolre/ioab020
PMCID:
PMC8111237
AbstractArticlePDF–1.9M
10.
Cdon mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly
Mingi Hong, Annabel Christ, Anna Christa, Thomas E Willnow, Robert S Krauss
eLife. 2020; 9: e60351. Published online 2020 Sep 2. doi: 10.7554/eLife.60351
PMCID:
PMC7467722
AbstractArticlePDF–2.9M
11.
Pivotal roles for eomesodermin during axis formation, epithelium-to-mesenchyme transition and endoderm specification in the mouse
Sebastian J. Arnold, Ulf K. Hofmann, Elizabeth K. Bikoff, Elizabeth J. Robertson
Development. Author manuscript; available in PMC 2020 Nov 18.
Published in final edited form as: Development. 2008 Feb 1; 135(3): 501–11. Published online 2008 Jan 2. doi: 10.1242/dev.014357
PMCID:
PMC7116389
AbstractArticlePDF–2.8M
12.
Single-cell analysis of cardiogenesis reveals basis for organ level developmental defects
T. Yvanka de Soysa, Sanjeev S. Ranade, Satoshi Okawa, Srikanth Ravichandran, Yu Huang, Hazel T. Salunga, Amelia Schricker, Antonio Del Sol, Casey A. Gifford, Deepak Srivastava
Nature. Author manuscript; available in PMC 2020 Jan 24.
Published in final edited form as: Nature. 2019 Aug; 572(7767): 120–124. Published online 2019 Jul 24. doi: 10.1038/s41586-019-1414-x
PMCID:
PMC6719697
AbstractArticlePDF–8.9M
13.
Zfp281 is essential for mouse epiblast maturation through transcriptional and epigenetic control of Nodal signaling
Xin Huang, Sophie Balmer, Fan Yang, Miguel Fidalgo, Dan Li, Diana Guallar, Anna-Katerina Hadjantonakis, Jianlong Wang
eLife. 2017; 6: e33333. Published online 2017 Nov 23. doi: 10.7554/eLife.33333
PMCID:
PMC5708896
AbstractArticlePDF–7.4M
14.
The epigenetic modifier Fam208a is required to maintain epiblast cell fitness
Shohag Bhargava, Brian Cox, Christiana Polydorou, Veronika Gresakova, Vladimir Korinek, Hynek Strnad, Radislav Sedlacek, Trevor Allan Epp, Kallayanee Chawengsaksophak
Sci Rep. 2017; 7: 9322. Published online 2017 Aug 24. doi: 10.1038/s41598-017-09490-w
Correction in:
Sci Rep. 2018; 8: 5762.
PMCID:
PMC5570896
AbstractArticlePDF–7.4M
15.
Cripto: Expression, epigenetic regulation and potential diagnostic use in testicular germ cell tumors
Cassy M. Spiller, Ad J.M. Gillis, Guillaume Burnet, Hans Stoop, Peter Koopman, Josephine Bowles, Leendert H.J. Looijenga
Mol Oncol. 2016 Apr; 10(4): 526–537. Published online 2015 Nov 18. doi: 10.1016/j.molonc.2015.11.003
PMCID:
PMC5423140
AbstractArticlePDF–2.2M
16.
A GPI processing phospholipase A2, PGAP6, modulates Nodal signaling in embryos by shedding CRIPTO
Gun-Hee Lee, Morihisa Fujita, Katsuyoshi Takaoka, Yoshiko Murakami, Yoshitaka Fujihara, Noriyuki Kanzawa, Kei-ichi Murakami, Eriko Kajikawa, Yoko Takada, Kazunobu Saito, Masahito Ikawa, Hiroshi Hamada, Yusuke Maeda, Taroh Kinoshita
J Cell Biol. 2016 Dec 5; 215(5): 705–718. doi: 10.1083/jcb.201605121
PMCID:
PMC5147002
AbstractArticlePDF–2.8M
17.
Ectopic expression of Cripto-1 in transgenic mouse embryos causes hemorrhages, fatal cardiac defects and embryonic lethality
Xiaolin Lin, Wentao Zhao, Junshuang Jia, Taoyan Lin, Gaofang Xiao, Shengchun Wang, Xia Lin, Yu Liu, Li Chen, Yujuan Qin, Jing Li, Tingting Zhang, Weichao Hao, Bangzhu Chen, Raoying Xie, Yushuang Cheng, Kang Xu, Kaitai Yao, Wenhua Huang, Dong Xiao, Yan Sun
Sci Rep. 2016; 6: 34501. Published online 2016 Sep 30. doi: 10.1038/srep34501
PMCID:
PMC5043281
AbstractArticlePDF–4.8M
18.
Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotency
Alessandro Fiorenzano, Emilia Pascale, Cristina D'Aniello, Dario Acampora, Cecilia Bassalert, Francesco Russo, Gennaro Andolfi, Mauro Biffoni, Federica Francescangeli, Ann Zeuner, Claudia Angelini, Claire Chazaud, Eduardo J. Patriarca, Annalisa Fico, Gabriella Minchiotti
Nat Commun. 2016; 7: 12589. Published online 2016 Sep 2. doi: 10.1038/ncomms12589
PMCID:
PMC5025790
AbstractArticlePDF–4.7M
19.
The ability of inner cell mass cells to self-renew as embryonic stem cells is acquired upon epiblast specification
Thorsten Boroviak, Remco Loos, Paul Bertone, Austin Smith, Jennifer Nichols
Nat Cell Biol. Author manuscript; available in PMC 2016 May 24.
Published in final edited form as: Nat Cell Biol. 2014 Jun; 16(6): 516–528. Published online 2014 May 25. doi: 10.1038/ncb2965
PMCID:
PMC4878656
AbstractArticlePDF–7.9M
20.
MEF2C regulates outflow tract alignment and transcriptional control of Tdgf1
Ralston M. Barnes, Ian S. Harris, Eric J. Jaehnig, Kimberly Sauls, Tanvi Sinha, Anabel Rojas, William Schachterle, David J. McCulley, Russell A. Norris, Brian L. Black
Development. 2016 Mar 1; 143(5): 774–779. doi: 10.1242/dev.126383
PMCID:
PMC4813332
AbstractArticle

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