Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yann Le Pétillon"'
Autor:
Rafath Chowdhury, Agnès Roure, Yann le Pétillon, Hélène Mayeur, Vladimir Daric, Sébastien Darras
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-25 (2022)
Abstract Background Vertebrates develop their peripheral nervous system (PNS) from transient unique embryonic structures, the neural crest, and the ectodermal placodes that are located at the border of the forming central nervous system. By contrast,
Externí odkaz:
https://doaj.org/article/bfd6d5e583524839a28c6a07aded8ae5
Autor:
Che-Yi Lin, Mei-Yeh Jade Lu, Jia-Xing Yue, Kun-Lung Li, Yann Le Pétillon, Luok Wen Yong, Yi-Hua Chen, Fu-Yu Tsai, Yu-Feng Lyu, Cheng-Yi Chen, Sheng-Ping L Hwang, Yi-Hsien Su, Jr-Kai Yu
Publikováno v:
PLoS Genetics, Vol 16, Iss 12, p e1009294 (2020)
Studies in various animals have shown that asymmetrically localized maternal transcripts play important roles in axial patterning and cell fate specification in early embryos. However, comprehensive analyses of the maternal transcriptomes with spatia
Externí odkaz:
https://doaj.org/article/d00f3ebf6c2747a1a09411e9f2a9d8d6
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119461 (2015)
Insulin is one of the most studied proteins since it is central to the regulation of carbohydrate and fat metabolism in vertebrates and its expression and release are disturbed in diabetes, the most frequent human metabolic disease worldwide. However
Externí odkaz:
https://doaj.org/article/e7cbf1d0fd9341fe88f51a71efbb8902
Autor:
Valérie Dupé, Véronique David, Isabelle Gicquel, Christèle Dubourg, Yann Le Pétillon, Claude Bendavid, Timothy P. Bohan, Sandra Mercier, Usha Kini, Georges Bourrouillou, Sylvie Odent, Christel Thauvin-Robinet, Lucie Rochard
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
Human Molecular Genetics, 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
Human Molecular Genetics, 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
International audience; Genetics of Holoprosencephaly (HPE), a congenital malformation of the developing human forebrain, is due to multiple genetic defects. Most genes that have been implicated in HPE belong to the sonic hedgehog signaling pathway.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0416e0669b3c99a84b9b35241338d90f
https://www.hal.inserm.fr/inserm-00554387/file/Dupe-2010-hum_mol_genet.pdf
https://www.hal.inserm.fr/inserm-00554387/file/Dupe-2010-hum_mol_genet.pdf
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e36554 (2012)
BACKGROUND: The basally divergent phylogenetic position of amphioxus (Cephalochordata), as well as its conserved morphology, development and genetics, make it the best proxy for the chordate ancestor. Particularly, studies using the amphioxus model h
Externí odkaz:
https://doaj.org/article/491c14babae1427f8dfbdff686b97115