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Claude Besmond

Showing results (1-10 of 41) with videos related to

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Journal of Biomedicine & Biotechnology|December 19, 2002
The Human Genome Revolution or Evolution?Claude Besmond, Marc Fellous
European Journal of Pediatrics|December 19, 2019
Exome sequencing of extreme phenotypes in bronchopulmonary dysplasiaAlice Hadchouel, Fabrice Decobert, Claude Besmond, et al.
Human Molecular Genetics|March 17, 2024
A loss of function mutation in CLDN25 causing Pelizaeus-Merzbacher-like leukodystrophyYosuke Hashimoto, Claude Besmond, Nathalie Boddaert, et al.
RNA (New York, N.Y.)|October 24, 2008
Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutionsMathieu Clément-Ziza, Arnold Munnich, Stanislas Lyonnet, et al.
Biotechniques|August 25, 2005
GeneRetriever: software to extract all genes and transcripts in between two genetic markers to assist design of human custom microarraysMathieu Clément-Ziza, Yehuda Brody, Arnold Munnich, et al.
Microbes and Infection|October 14, 2003
Enhanced cloning efficiency of mouse bone marrow macrophage progenitors correlates with increased content of CSF-1 receptor of their progeny at low oxygen tensionStéphane Flamant, Maï Lebastard, Pascale Pescher, et al.
Schizophrenia Research|December 3, 2017
Somatic mosaicism for SLC1A1 mutation supports threshold effect and familial aggregation in schizophrenia spectrum disordersCaroline Demily, Laurence Hubert, Nicolas Franck, et al.
Human Mutation|June 7, 2017
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsyKarine Poirier, Laurence Hubert, Géraldine Viot, et al.
BMC Genomics|May 28, 2009
Evaluation of methods for amplification of picogram amounts of total RNA for whole genome expression profilingMathieu Clément-Ziza, David Gentien, Stanislas Lyonnet, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|August 10, 2017
Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathyClaude Besmond, Dominique Valla, Laurence Hubert, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Journal of Biomedicine & Biotechnology|December 19, 2002
The Human Genome Revolution or Evolution?Claude Besmond, Marc Fellous
European Journal of Pediatrics|December 19, 2019
Exome sequencing of extreme phenotypes in bronchopulmonary dysplasiaAlice Hadchouel, Fabrice Decobert, Claude Besmond, et al.
Human Molecular Genetics|March 17, 2024
A loss of function mutation in CLDN25 causing Pelizaeus-Merzbacher-like leukodystrophyYosuke Hashimoto, Claude Besmond, Nathalie Boddaert, et al.
RNA (New York, N.Y.)|October 24, 2008
Stabilization of RNA during laser capture microdissection by performing experiments under argon atmosphere or using ethanol as a solvent in staining solutionsMathieu Clément-Ziza, Arnold Munnich, Stanislas Lyonnet, et al.
Biotechniques|August 25, 2005
GeneRetriever: software to extract all genes and transcripts in between two genetic markers to assist design of human custom microarraysMathieu Clément-Ziza, Yehuda Brody, Arnold Munnich, et al.
Microbes and Infection|October 14, 2003
Enhanced cloning efficiency of mouse bone marrow macrophage progenitors correlates with increased content of CSF-1 receptor of their progeny at low oxygen tensionStéphane Flamant, Maï Lebastard, Pascale Pescher, et al.
Schizophrenia Research|December 3, 2017
Somatic mosaicism for SLC1A1 mutation supports threshold effect and familial aggregation in schizophrenia spectrum disordersCaroline Demily, Laurence Hubert, Nicolas Franck, et al.
Human Mutation|June 7, 2017
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsyKarine Poirier, Laurence Hubert, Géraldine Viot, et al.
BMC Genomics|May 28, 2009
Evaluation of methods for amplification of picogram amounts of total RNA for whole genome expression profilingMathieu Clément-Ziza, David Gentien, Stanislas Lyonnet, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|August 10, 2017
Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathyClaude Besmond, Dominique Valla, Laurence Hubert, et al.
Pageof 5