Search research articles
Contact Us
Filters
Showing results (61-70 of 225) with videos related to
Page
of 23
Sort By:
Biotechniques
|
May 22, 2002
Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing
B Neve, P Froguel, L Corset, et al.
Diabetologia
|
January 25, 2007
A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population
M Horikoshi, K Hara, C Ito, et al.
Diabetes
|
July 1, 1997
Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2q
E H Hani, J Hager, A Philippi, et al.
The Journal of Clinical Investigation
|
July 21, 2000
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
C Vaisse, K Clement, E Durand, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 1, 1994
Phenotyping is an accurate means of analysing the principal apolipoprotein E isoforms
R W James, J Ruiz, H Blanché, et al.
Diabetes & Metabolism
|
March 1, 1997
Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?
A Ktorza, C Bernard, V Parent, et al.
Biotechniques
|
May 1, 1994
Nonradioactive screening of glucokinase mutations in maturity onset diabetes of the young
H Blanché, J Hager, F Sun, et al.
The Journal of Biological Chemistry
|
December 10, 1999
Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations
M Vaxillaire, A Abderrahmani, P Boutin, et al.
Diabetologia
|
December 29, 2000
An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohort
A Meirhaeghe, P Amouyel, N Helbecque, et al.
Diabetes
|
May 20, 1998
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians
J C Chèvre, E H Hani, D A Stoffers, et al.
Page
of 23
Search research articles
Search
Showing results (61-70 of 225) with videos related to
Sort By:
Page
of 23
Biotechniques
|
May 22, 2002
Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing
B Neve, P Froguel, L Corset, et al.
Diabetologia
|
January 25, 2007
A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population
M Horikoshi, K Hara, C Ito, et al.
Diabetes
|
July 1, 1997
Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2q
E H Hani, J Hager, A Philippi, et al.
The Journal of Clinical Investigation
|
July 21, 2000
Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity
C Vaisse, K Clement, E Durand, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 1, 1994
Phenotyping is an accurate means of analysing the principal apolipoprotein E isoforms
R W James, J Ruiz, H Blanché, et al.
Diabetes & Metabolism
|
March 1, 1997
Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?
A Ktorza, C Bernard, V Parent, et al.
Biotechniques
|
May 1, 1994
Nonradioactive screening of glucokinase mutations in maturity onset diabetes of the young
H Blanché, J Hager, F Sun, et al.
The Journal of Biological Chemistry
|
December 10, 1999
Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations
M Vaxillaire, A Abderrahmani, P Boutin, et al.
Diabetologia
|
December 29, 2000
An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohort
A Meirhaeghe, P Amouyel, N Helbecque, et al.
Diabetes
|
May 20, 1998
Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians
J C Chèvre, E H Hani, D A Stoffers, et al.
Page
of 23