Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Jacques J Picard"'
Autor:
Nata Y S-G Diman, Sophie Remacle, Nicolas Bertrand, Jacques J Picard, Stéphane Zaffran, René Rezsohazy
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27624 (2011)
A transgenic mouse line harbouring a β-galacdosidase reporter gene controlled by the proximal 2 kb promoter of Hoxa3 was previously generated to investigate the regulatory cues governing Hoxa3 expression in the mouse. Examination of transgenic embry
Externí odkaz:
https://doaj.org/article/90b2d26c803d4161b1e1ee8f6eb924ee
Autor:
Sophie Remacle, Omar Abdel O.A. Samad, Xavier Lampe, Jacques J. Picard, Allan Guiguen, René Rezsohazy, Filippo F.M. Rijli, Christelle Matis
Publikováno v:
Nucleic acids research, 36 (10
Nucleic Acids Research
Nucleic Acids Research, 2008, 36 (10), pp.3214-25. ⟨10.1093/nar/gkn148⟩
Nucleic Acids Research, Oxford University Press, 2008, 36 (10), pp.3214-25. ⟨10.1093/nar/gkn148⟩
Nucleic Acids Research, Vol. 36, no. 10, p. 3214-25 (2008)
Nucleic Acids Research
Nucleic Acids Research, 2008, 36 (10), pp.3214-25. ⟨10.1093/nar/gkn148⟩
Nucleic Acids Research, Oxford University Press, 2008, 36 (10), pp.3214-25. ⟨10.1093/nar/gkn148⟩
Nucleic Acids Research, Vol. 36, no. 10, p. 3214-25 (2008)
The Hoxa2 gene has a fundamental role in vertebrate craniofacial and hindbrain patterning. Segmental control of Hoxa2 expression is crucial to its function and several studies have highlighted transcriptional regulatory elements governing its activit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::528eb8ca4ae3d88b040906c489608a09
https://doi.org/10.1093/nar/gkn148
https://doi.org/10.1093/nar/gkn148
Autor:
Jacques J. Picard, Mehdi Maleki, René Rezsohazy, Philippe Delahaut, Pierre Henri Deprez, Laurent Massip, Benoît Lengelé, Catherine Behets, F. Ectors
Publikováno v:
Differentiation. 75:256-267
Vertebrate Hox genes act as developmental architects by patterning embryonic structures like axial skeletal elements, limbs, brainstem territories, or neural crest derivatives. While active during the patterning steps of development, these genes turn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ede306d69a9c6801794b2ee0897932
https://doi.org/10.1111/j.1432-0436.2006.00132.x
https://doi.org/10.1111/j.1432-0436.2006.00132.x
Autor:
Jacques J. Picard, Sophie Remacle, René Rezsohazy, Xavier Lampe, Christelle Matis, Filippo F.M. Rijli, Françoise Gofflot, Franck Oury
Publikováno v:
Developmental Dynamics
Developmental Dynamics, Wiley, 2007, 236 (9), pp.2675-84. ⟨10.1002/dvdy.21266⟩
Developmental Dynamics, Wiley, 2007, 236 (9), pp.2675-84. ⟨10.1002/dvdy.21266⟩
The embryonic functions of Hox proteins have been extensively investigated in several animal phyla. These transcription factors act as selectors of developmental programmes, to govern the morphogenesis of multiple structures and organs. However, desp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec78d7fd95f2b24adbe35ef7b467943
https://doi.org/10.1002/dvdy.21266
https://doi.org/10.1002/dvdy.21266
Publikováno v:
Reproductive Toxicology. 20:39-45
Several embryotoxic agents, which includes sodium salicylate, were reported to induce vertebral variations in the form of supernumerary ribs (SNR) when administered to pregnant rodents. Because the biological significance of SNR in toxicological stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::522b5d1ce1b8e8c58b2558b3a2c4e1bd
https://doi.org/10.1016/j.reprotox.2004.12.014
https://doi.org/10.1016/j.reprotox.2004.12.014
Publikováno v:
Diabetologia. 46:1245-1251
Aims/hypothesis. Maternal diabetes mellitus increases the risk for fetal malformations. Several of these malformations are found in organs and tissues derived from the neural crest. Previous studies have shown changes in fetal organs of neural crest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba63ea09714081200aad135f001f9e3d
https://doi.org/10.1007/s00125-003-1100-1
https://doi.org/10.1007/s00125-003-1100-1
Autor:
Jacques J. Picard, Charles Roux, Claude Wolf, Françoise Chevy, Françoise Illien, Carine Hars, Françoise Gofflot
Publikováno v:
Human Molecular Genetics. 12:1187-1198
Human disorders caused by inborn errors of cholesterol biosynthesis are characterized by dysmorphogenesis of multiple organs. This includes limb malformations that are observed at high frequency in some disorders, such as the Smith-Lemli-Opitz syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d511f88502fefe8d4c0b093a20c3d6
https://doi.org/10.1093/hmg/ddg129
https://doi.org/10.1093/hmg/ddg129
Autor:
Michael G. Narotsky, Jacques J. Picard, Nathalie Pacico, Françoise Gofflot, Nathalie Wéry, Robert J. Kavlock
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 67:59-67
BACKGROUND: Previously, we showed that prenatal exposure to boric acid (BA), an industrial agent with large production, causes alterations of the axial skeleton in rat embryos, reminiscent of homeotic transformations. Indeed, Sprague-Dawley rats expo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::215e0c7697074d3341b3d0d1a62b47e8
https://doi.org/10.1002/bdra.10031
https://doi.org/10.1002/bdra.10031
Publikováno v:
Developmental Dynamics. 220:99-111
Holoprosencephaly is a common developmental anomaly of the forebrain and midface, that has been associated with mutations in the Sonic Hedgehog gene, and with perturbations of cholesterol synthesis and metabolism in mammalian embryos. The study prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf05dd32b164f5ff61b74ec12f4cba4
https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1092>3.0.co
https://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1092>3.0.co
Publikováno v:
Mammalian Genome. 11:696-699
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4167bc76ad72e22fe28f17078c473b14
https://doi.org/10.1007/s003350010116
https://doi.org/10.1007/s003350010116