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C Dina

Showing results (1-10 of 35) with videos related to

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Diabetologia|July 12, 2003
PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian populationC Lopes, C Dina, E Durand, et al.
Genetic Epidemiology|January 1, 1997
Empirical affected-sib-pair statistics: two simulation strategiesC Dina, J C Buzzi, F Demenais, et al.
Diabetes & Metabolism|January 14, 2000
Absence of replication in the French population of the association between beta 2/NEUROD-A45T polymorphism and type 1 diabetesS Dupont, C Dina, E H Hani, et al.
Gene|August 5, 1994
Genomic structure of the downstream part of the human FLT3 gene: exon/intron structure conservation among genes encoding receptor tyrosine kinases (RTK) of subclass IIIF Agnès, B Shamoon, C Dina, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 24, 2004
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitusC Lacquemant, P Froguel, S Lobbens, et al.
Diabetologia|April 11, 2003
Does the -11377 promoter variant of APM1 gene contribute to the genetic risk for Type 2 diabetes mellitus in Japanese families?C Populaire, Y Mori, C Dina, et al.
Molecular Psychiatry|January 19, 2005
Dopaminergic polymorphisms associated with self-report measures of human altruism: a fresh phenotype for the dopamine D4 receptorR Bachner-Melman, I Gritsenko, L Nemanov, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French CaucasiansE H Hani, S Dupont, E Durand, et al.
Diabetologia|February 7, 2001
A genetic variation in the 5' flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activityS Otabe, K Clement, C Dina, et al.
Molecular Psychiatry|March 8, 2006
Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skillsN Yirmiya, C Rosenberg, S Levi, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Diabetologia|July 12, 2003
PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian populationC Lopes, C Dina, E Durand, et al.
Genetic Epidemiology|January 1, 1997
Empirical affected-sib-pair statistics: two simulation strategiesC Dina, J C Buzzi, F Demenais, et al.
Diabetes & Metabolism|January 14, 2000
Absence of replication in the French population of the association between beta 2/NEUROD-A45T polymorphism and type 1 diabetesS Dupont, C Dina, E H Hani, et al.
Gene|August 5, 1994
Genomic structure of the downstream part of the human FLT3 gene: exon/intron structure conservation among genes encoding receptor tyrosine kinases (RTK) of subclass IIIF Agnès, B Shamoon, C Dina, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 24, 2004
The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non-insulin-dependent) diabetes mellitusC Lacquemant, P Froguel, S Lobbens, et al.
Diabetologia|April 11, 2003
Does the -11377 promoter variant of APM1 gene contribute to the genetic risk for Type 2 diabetes mellitus in Japanese families?C Populaire, Y Mori, C Dina, et al.
Molecular Psychiatry|January 19, 2005
Dopaminergic polymorphisms associated with self-report measures of human altruism: a fresh phenotype for the dopamine D4 receptorR Bachner-Melman, I Gritsenko, L Nemanov, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French CaucasiansE H Hani, S Dupont, E Durand, et al.
Diabetologia|February 7, 2001
A genetic variation in the 5' flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activityS Otabe, K Clement, C Dina, et al.
Molecular Psychiatry|March 8, 2006
Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skillsN Yirmiya, C Rosenberg, S Levi, et al.
Pageof 4