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Fabien Guimiot

Showing results (61-70 of 92) with videos related to

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Stem Cell Reports|November 20, 2018
Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi AnemiaCarine Domenech, Loïc Maillard, Alix Rousseau, et al.
Acta Neuropathologica Communications|May 3, 2017
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ genePascale Saugier-Veber, Florent Marguet, François Lecoquierre, et al.
Immunity|February 14, 2006
Dynamics of thymus-colonizing cells during human developmentRima Haddad, Fabien Guimiot, Emmanuelle Six, et al.
Regulatory Toxicology and Pharmacology : RTP|December 3, 2015
Safety study of Ciprofloxacin in newborn miceThomas Bourgeois, Anne-Lise Delezoide, Wei Zhao, et al.
Nature Cell Biology|March 29, 2024
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortexLaure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, et al.
American Journal of Medical Genetics. Part A|July 1, 2014
Inversion duplication deletions involving the long arm of chromosome 13: phenotypic description of additional three fetuses and genotype-phenotype correlationChloe Quelin, Emmanuel Spaggiari, Suonavy Khung-Savatovsky, et al.
American Journal of Human Genetics|September 13, 2016
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal ArthrogryposisJérôme Maluenda, Constance Manso, Loic Quevarec, et al.
Genes|June 26, 2025
<i>MPDZ</i> Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle AtresiaSara Cabet, Jean-François Ghersi-Egea, Suonavy Khung-Savatovsky, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 geneAndrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, et al.
Neurology. Genetics|March 28, 2025
Radial Microbrain (Micrencephaly) Is Caused by a Recurrent Variant in the <i>RTTN</i> GeneClarisse Gins, Fabien Guimiot, Séverine Drunat, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
Stem Cell Reports|November 20, 2018
Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi AnemiaCarine Domenech, Loïc Maillard, Alix Rousseau, et al.
Acta Neuropathologica Communications|May 3, 2017
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ genePascale Saugier-Veber, Florent Marguet, François Lecoquierre, et al.
Immunity|February 14, 2006
Dynamics of thymus-colonizing cells during human developmentRima Haddad, Fabien Guimiot, Emmanuelle Six, et al.
Regulatory Toxicology and Pharmacology : RTP|December 3, 2015
Safety study of Ciprofloxacin in newborn miceThomas Bourgeois, Anne-Lise Delezoide, Wei Zhao, et al.
Nature Cell Biology|March 29, 2024
A cell fate decision map reveals abundant direct neurogenesis bypassing intermediate progenitors in the human developing neocortexLaure Coquand, Clarisse Brunet Avalos, Anne-Sophie Macé, et al.
American Journal of Medical Genetics. Part A|July 1, 2014
Inversion duplication deletions involving the long arm of chromosome 13: phenotypic description of additional three fetuses and genotype-phenotype correlationChloe Quelin, Emmanuel Spaggiari, Suonavy Khung-Savatovsky, et al.
American Journal of Human Genetics|September 13, 2016
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal ArthrogryposisJérôme Maluenda, Constance Manso, Loic Quevarec, et al.
Genes|June 26, 2025
<i>MPDZ</i> Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle AtresiaSara Cabet, Jean-François Ghersi-Egea, Suonavy Khung-Savatovsky, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 geneAndrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, et al.
Neurology. Genetics|March 28, 2025
Radial Microbrain (Micrencephaly) Is Caused by a Recurrent Variant in the <i>RTTN</i> GeneClarisse Gins, Fabien Guimiot, Séverine Drunat, et al.
Pageof 10