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Marie-José Perez

Showing results (1-10 of 12) with videos related to

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The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|May 5, 2007
Epithelial phenotypes in the developing human prostateGuy Letellier, Marie-José Perez, Mokrane Yacoub, et al.
Pediatrics|May 3, 2008
Decreased full breastfeeding, altered practices, perceptions, and infant weight change of prepregnant obese women: a need for extra supportElise Mok, Clarisse Multon, Lorraine Piguel, et al.
Epigenetics|May 1, 2014
A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivoAnne Bergougnoux, Isabelle Rivals, Alessandro Liquori, et al.
Human Gene Therapy|June 29, 2013
Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathyJohn Rendu, Julie Brocard, Eric Denarier, et al.
American Journal of Human Genetics|January 21, 2014
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansCamille Humbert, Flora Silbermann, Bharti Morar, et al.
Journal of Medical Genetics|April 14, 2012
NEK1 and DYNC2H1 are both involved in short rib polydactyly Majewski type but not in Beemer Langer casesJoyce El Hokayem, Céline Huber, Adeline Couvé, et al.
Acta Neuropathologica|July 4, 2013
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular basesHoma Adle-Biassette, Pascale Saugier-Veber, Catherine Fallet-Bianco, et al.
Journal of Medical Genetics|October 2, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutationsMarine Legendre, Marie Gonzales, Géraldine Goudefroye, et al.
Brain : a Journal of Neurology|February 11, 2012
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathiesLouise Devisme, Céline Bouchet, Marie Gonzalès, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2015
Treacher Collins syndrome: a clinical and molecular study based on a large series of patientsMarie Vincent, David Geneviève, Agnès Ostertag, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|May 5, 2007
Epithelial phenotypes in the developing human prostateGuy Letellier, Marie-José Perez, Mokrane Yacoub, et al.
Pediatrics|May 3, 2008
Decreased full breastfeeding, altered practices, perceptions, and infant weight change of prepregnant obese women: a need for extra supportElise Mok, Clarisse Multon, Lorraine Piguel, et al.
Epigenetics|May 1, 2014
A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivoAnne Bergougnoux, Isabelle Rivals, Alessandro Liquori, et al.
Human Gene Therapy|June 29, 2013
Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathyJohn Rendu, Julie Brocard, Eric Denarier, et al.
American Journal of Human Genetics|January 21, 2014
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansCamille Humbert, Flora Silbermann, Bharti Morar, et al.
Journal of Medical Genetics|April 14, 2012
NEK1 and DYNC2H1 are both involved in short rib polydactyly Majewski type but not in Beemer Langer casesJoyce El Hokayem, Céline Huber, Adeline Couvé, et al.
Acta Neuropathologica|July 4, 2013
Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular basesHoma Adle-Biassette, Pascale Saugier-Veber, Catherine Fallet-Bianco, et al.
Journal of Medical Genetics|October 2, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutationsMarine Legendre, Marie Gonzales, Géraldine Goudefroye, et al.
Brain : a Journal of Neurology|February 11, 2012
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathiesLouise Devisme, Céline Bouchet, Marie Gonzalès, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2015
Treacher Collins syndrome: a clinical and molecular study based on a large series of patientsMarie Vincent, David Geneviève, Agnès Ostertag, et al.
Pageof 2