Transcriptional analysis of abdominal fat in chickens divergently selected on bodyweight at two ages reveals novel mechanisms controlling adiposity: validating visceral adipose tissue as a dynamic endocrine and metabolic organ

Autor: C. W. Resnyk, W. Carré, X. Wang, T. E. Porter, J. Simon, E. Le Bihan-Duval, M. J. Duclos, S. E. Aggrey, L. A. Cogburn

Publikováno v: BMC Genomics, Vol 18, Iss 1, Pp 1-31 (2017)

Abstract Background Decades of intensive genetic selection in the domestic chicken (Gallus gallus domesticus) have enabled the remarkable rapid growth of today’s broiler (meat-type) chickens. However, this enhanced growth rate was accompanied by se

Externí odkaz: https://doaj.org/article/023c161ab30046d5bf512cfbf75a3f10

Identification du premier cas autochtone de xeroderma pigmentosum de type A en France : mutation homozygote XPA H244R contrastant avec un phénotype modéré sans atteinte neurologique

Autor: T. Menez, C. Moisson-Franckhauser, W. Carré, A. Dupuy, D. Russo, Lise Boussemart, Catherine Droitcourt, Monica Dinulescu, Alain Sarasin, C. Dubourg, Henri Adamski, S. Law Ping Man

Publikováno v: Annales de Dermatologie et de Vénéréologie. 146:A250

Introduction Le xeroderma pigmentosum (XP) est une maladie genetique autosomique recessive rare touchant 1 cas/1 million de naissances en Europe. Elle est liee a un defaut du systeme de reparation de l’ADN « nucleotide excision repair », post-exp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4adca6246fe8d928e0dcde4fcd937bc5
https://doi.org/10.1016/j.annder.2019.09.394

Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing

Autor: C, Mouden, C, Dubourg, W, Carré, S, Rose, C, Quelin, L, Akloul, H, Hamdi-Rozé, G, Viot, H, Salhi, P, Darnault, S, Odent, V, Dupé, V, David

Publikováno v: Clinical Genetics
Clinical Genetics, 2016, 89 (6), pp.659-668. ⟨10.1111/cge.12722⟩
Clinical Genetics, Wiley, 2016, in press. <10.1111/cge.12722>
Clinical Genetics, Wiley, 2016, 89 (6), pp.659-668. ⟨10.1111/cge.12722⟩

International audience; Holoprosencephaly (HPE) is the most common congenital cerebral malformation, characterized by impaired forebrain cleavage and midline facial anomalies. Heterozygous mutations in 14 genes have been associated with HPE, and are

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7cfea2c511d4608d8a09e3dbdc3271c8
https://univ-rennes.hal.science/hal-01259228

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