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C Vigouroux

Showing results (41-50 of 68) with videos related to

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Diabetes|March 31, 1998
Human hormone-sensitive lipase: genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDMJ Magré, H Laurell, C Fizames, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1992
[Cytomegalovirus infections in patients after liver transplantation: determination of risk groups]C Vigouroux, C Moncorgé, Y Calmus, et al.
Diabetes & Metabolism|October 16, 2007
Efficacy of pioglitazone in familial partial lipodystrophy of the Dunnigan type: a case reportF Moreau, S Boullu-Sanchis, C Vigouroux, et al.
Diabetes|March 1, 1994
Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genesM Vaxillaire, N Vionnet, C Vigouroux, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1988
[109 orthotopic hepatic transplantations. Evaluation of our experience]Y Chapuis, D Houssin, N Pras-Jude, et al.
Cell Death and Differentiation|July 7, 2007
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescenceM Caron, M Auclair, B Donadille, et al.
Nature Genetics|April 1, 1995
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12qM Vaxillaire, V Boccio, A Philippi, et al.
Diabetes|November 14, 1997
Dominant transmission of insulin resistance in a type A family resulting from a heterozygous nonsense mutation in the insulin receptor gene and associated with decreased mRNA level and insulin binding sitesJ Magré, C Karayanni, C G Hadjiathanasiou, et al.
Seminars in Cell & Developmental Biology|January 4, 2014
Nuclear envelope-related lipodystrophiesA C Guénantin, N Briand, G Bidault, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous familiesC Vigouroux, E Khallouf, C Bourut, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Diabetes|March 31, 1998
Human hormone-sensitive lipase: genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDMJ Magré, H Laurell, C Fizames, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1992
[Cytomegalovirus infections in patients after liver transplantation: determination of risk groups]C Vigouroux, C Moncorgé, Y Calmus, et al.
Diabetes & Metabolism|October 16, 2007
Efficacy of pioglitazone in familial partial lipodystrophy of the Dunnigan type: a case reportF Moreau, S Boullu-Sanchis, C Vigouroux, et al.
Diabetes|March 1, 1994
Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genesM Vaxillaire, N Vionnet, C Vigouroux, et al.
Chirurgie; Memoires De L'Academie De Chirurgie|January 1, 1988
[109 orthotopic hepatic transplantations. Evaluation of our experience]Y Chapuis, D Houssin, N Pras-Jude, et al.
Cell Death and Differentiation|July 7, 2007
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescenceM Caron, M Auclair, B Donadille, et al.
Nature Genetics|April 1, 1995
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12qM Vaxillaire, V Boccio, A Philippi, et al.
Diabetes|November 14, 1997
Dominant transmission of insulin resistance in a type A family resulting from a heterozygous nonsense mutation in the insulin receptor gene and associated with decreased mRNA level and insulin binding sitesJ Magré, C Karayanni, C G Hadjiathanasiou, et al.
Seminars in Cell & Developmental Biology|January 4, 2014
Nuclear envelope-related lipodystrophiesA C Guénantin, N Briand, G Bidault, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous familiesC Vigouroux, E Khallouf, C Bourut, et al.
Pageof 7