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G Raux

Showing results (11-20 of 21) with videos related to

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Journal of Medical Genetics|January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH geneH Jacquet, J Berthelot, C Bonnemains, et al.
Neurology|November 30, 2000
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutationG Raux, R Gantier, C Thomas-Anterion, et al.
Molecular Psychiatry|October 22, 2003
The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficitE Houy, G Raux, F Thibaut, et al.
Cancer Research|June 13, 2000
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragmentsF Charbonnier, G Raux, Q Wang, et al.
Leukemia|May 15, 2007
Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patientsC Bastard, G Raux, C Fruchart, et al.
Molecular Psychiatry|October 26, 2002
The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficitG Raux, F Bonnet-Brilhault, S Louchart, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.
Genes and Immunity|February 22, 2002
Pemphigus is not associated with allotypic markers of immunoglobulin kappaM Zitouni, P Martel, M Ben Ayed, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|January 15, 2003
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH geneH Jacquet, J Berthelot, C Bonnemains, et al.
Neurology|November 30, 2000
Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutationG Raux, R Gantier, C Thomas-Anterion, et al.
Molecular Psychiatry|October 22, 2003
The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficitE Houy, G Raux, F Thibaut, et al.
Cancer Research|June 13, 2000
Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragmentsF Charbonnier, G Raux, Q Wang, et al.
Leukemia|May 15, 2007
Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patientsC Bastard, G Raux, C Fruchart, et al.
Molecular Psychiatry|October 26, 2002
The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficitG Raux, F Bonnet-Brilhault, S Louchart, et al.
European Journal of Human Genetics : EJHG|September 12, 2000
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French populationL Zurutuza, P Verpillat, G Raux, et al.
Genes and Immunity|February 22, 2002
Pemphigus is not associated with allotypic markers of immunoglobulin kappaM Zitouni, P Martel, M Ben Ayed, et al.
Neurology|February 28, 2007
Variations in the APP gene promoter region and risk of Alzheimer diseaseL Guyant-Maréchal, A Rovelet-Lecrux, L Goumidi, et al.
American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.
Pageof 3