Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jean François Lemaitre"'
Autor:
Rylan Shearn, Alison E Wright, Sylvain Mousset, Corinne Régis, Simon Penel, Jean-François Lemaitre, Guillaume Douay, Brigitte Crouau-Roy, Emilie Lecompte, Gabriel AB Marais
Publikováno v:
eLife, Vol 9 (2020)
Sex chromosomes are typically comprised of a non-recombining region and a recombining pseudoautosomal region. Accurately quantifying the relative size of these regions is critical for sex-chromosome biology both from a functional and evolutionary per
Externí odkaz:
https://doaj.org/article/bf5d61d2898b4167aa525d8f1e5e5797
Autor:
Frédéric Thomas, Mathieu Giraudeau, François Renaud, Beata Ujvari, Benjamin Roche, Pascal Pujol, Michel Raymond, Jean-François Lemaitre, Alexandra Alvergne
Publikováno v:
PLoS Biology, Vol 17, Iss 12, p e3000565 (2019)
Why a postfertile stage has evolved in females of some species has puzzled evolutionary biologists for over 50 years. We propose that existing adaptive explanations have underestimated in their formulation an important parameter operating both at the
Externí odkaz:
https://doaj.org/article/be6ce05607f04f9dbcdfd39ef772b08a
Autor:
Cayuela, Hugo, Kurtuluş Olgun, Angelini, Claudio, Üzüm, Nazan, Peyronel, Olivier, Miaud, Claude, Avcı, Aziz, Jean-François Lemaitre, Schmidt, Benedikt R.
Actuarial senescence has been viewed for a long time as an inevitable and uniform process. However, the work on senescence has mainly focused on endotherms with deterministic growth and low regeneration capacity during the adult stage, leading to a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::251da7e234cb8eeede237d6a32744439
Autor:
Ahmed Fatmi, Pierre L. Roubertoux, Joris Andrieux, Catherine Vincent-Delorme, Michèle Carlier, Paolo Gubellini, Laurence Had-Aissouni, Fatimetou Abderrehamane, Bénédicte Duban, Agne Liedén, Detlef Bockenhauer, Emeric Dubois, Mehdi Metwaly, Adrian S. Woolf, Nenad Sestan, Dany Severac, Jean Marie Cuisset, Laurent Fasano, Jean François Lemaitre, Marwan Shinawi, Marie Pierre Lemaitre, Lydia Kerkerian-Le Goff, Eva Rudd, Xavier Caubit, Pascal Salin, Bernard Jacq, Alistair N. Garratt, Kenneth Y. Kwan, Ying Zhu
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature Genetics, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature genetics
Caubit, X, Gubellini, P, Andrieux, J, Roubertoux, P L, Metwaly, M, Jacq, B, Fatmi, A, Had-Aissouni, L, Kwan, K Y, Salin, P, Carlier, M, Liedén, A, Rudd, E, Shinawi, M, Vincent-Delorme, C, Cuisset, J-M, Lemaitre, M-P, Fatimetou, A, Duban, B, Lemaitre, J-F, Woolf, A S, Bockenhauer, D, Severac, D, Dubois, E, Zhu, Y, Sestan, N, Garratt, A N, Kerkerian-Le Goff, L & Fasano, L 2016, ' TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons ', Nature Genetics, vol. 48, pp. 1359-1369 . https://doi.org/10.1038/ng.3681
Nature Genetics, Nature Publishing Group, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature Genetics, 2016, 48 (11), pp.1359-1369. ⟨10.1038/ng.3681⟩
Nature genetics
Caubit, X, Gubellini, P, Andrieux, J, Roubertoux, P L, Metwaly, M, Jacq, B, Fatmi, A, Had-Aissouni, L, Kwan, K Y, Salin, P, Carlier, M, Liedén, A, Rudd, E, Shinawi, M, Vincent-Delorme, C, Cuisset, J-M, Lemaitre, M-P, Fatimetou, A, Duban, B, Lemaitre, J-F, Woolf, A S, Bockenhauer, D, Severac, D, Dubois, E, Zhu, Y, Sestan, N, Garratt, A N, Kerkerian-Le Goff, L & Fasano, L 2016, ' TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons ', Nature Genetics, vol. 48, pp. 1359-1369 . https://doi.org/10.1038/ng.3681
International audience; TSHZ3, which encodes a zinc-finger transcription factor, was recently positioned as a hub gene in a module of the genes with the highest expression in the developing human neocortex, but its functions remained unknown. Here we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1526d52f0caf1ad65c8793faee92cf7
https://hal.archives-ouvertes.fr/hal-01432295
https://hal.archives-ouvertes.fr/hal-01432295
Publikováno v:
Vascular health and risk management, 11
Vascular Health and Risk Management
Vascular Health and Risk Management
Massive hemorrhage in tracheostomy patients is generally described as a result of a tracheoinnominate artery fistula. Other etiologies for rupture of a false aneurysm are rare. The classical procedure for subclavian artery aneurysm is open surgery. E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87bf1beac5b3ccdc59697f3bf58a0260
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/218672
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/218672
Autor:
Bruno Delobel, Bruno Leheup, Jean-François Lemaitre, Jean-Michel Pinoit, Karine Poirier, Nadia Bahi-Buisson, Christophe Philippe, Sophie Julia, Bénédicte Demeer, Jamel Chelly, Anne de Saint-Martin, Mireille Cossée, Heifa Hichri, Jean-Louis Mandel, Didier Devys, Vincent Laugel, Laurence Faivre, Valérie Biancalana
Publikováno v:
American journal of medical genetics. Part A. (1)
Mutations in the ARX gene cause both nonsyndromic and several forms of syndromic mental retardation (MR). Two polyalanine (polyA) expansions of ARX are recurrent mutations. The most common one, the c.428_451dup, is associated with a wide spectrum of