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F Demenais

Showing results (71-80 of 103) with videos related to

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Human Molecular Genetics|March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study GroupN Soufir, M F Avril, A Chompret, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|June 1, 1989
Genetic susceptibility to leprosy on a Caribbean Island: linkage analysis with five markersL Abel, F Demenais, M S Baule, et al.
Revue Des Maladies Respiratoires|July 23, 2009
[GA2LEN (Global Allergy and Asthma European Network)]J Bousquet, F Kauffmann, P Demoly, et al.
Genetic Epidemiology|January 1, 1995
Detection of a recessive major gene for high IgE levels acting independently of specific response to allergensM H Dizier, M Hill, A James, et al.
Melanoma Research|May 3, 2001
Association between germ cell tumours, large numbers of naevi, atypical naevi and melanomaM F Avril, A Chompret, L Verne-Fourment, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Genetic analysis of diabetes and insulitis in an interspecific cross of the nonobese diabetic mouse with Mus spretusB de Gouyon, E Melanitou, M F Richard, et al.
Familial Cancer|June 2, 2009
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypesValérie Chaudru, M T Lo, F Lesueur, et al.
Scientific Reports|April 22, 2017
Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthmaY Liu, M Brossard, C Sarnowski, et al.
Genes, Chromosomes & Cancer|October 2, 2001
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effectS Auroy, M F Avril, A Chompret, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|March 21, 1998
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study GroupN Soufir, M F Avril, A Chompret, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|June 1, 1989
Genetic susceptibility to leprosy on a Caribbean Island: linkage analysis with five markersL Abel, F Demenais, M S Baule, et al.
Revue Des Maladies Respiratoires|July 23, 2009
[GA2LEN (Global Allergy and Asthma European Network)]J Bousquet, F Kauffmann, P Demoly, et al.
Genetic Epidemiology|January 1, 1995
Detection of a recessive major gene for high IgE levels acting independently of specific response to allergensM H Dizier, M Hill, A James, et al.
Melanoma Research|May 3, 2001
Association between germ cell tumours, large numbers of naevi, atypical naevi and melanomaM F Avril, A Chompret, L Verne-Fourment, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Genetic analysis of diabetes and insulitis in an interspecific cross of the nonobese diabetic mouse with Mus spretusB de Gouyon, E Melanitou, M F Richard, et al.
Familial Cancer|June 2, 2009
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypesValérie Chaudru, M T Lo, F Lesueur, et al.
Scientific Reports|April 22, 2017
Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthmaY Liu, M Brossard, C Sarnowski, et al.
Genes, Chromosomes & Cancer|October 2, 2001
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effectS Auroy, M F Avril, A Chompret, et al.
The Journal of Clinical Investigation|March 21, 1998
A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitusE H Hani, L Suaud, P Boutin, et al.
Pageof 11