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- 2007
-
Mark
Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
(
- Contribution to journal › Article
-
Mark
Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
(
- Contribution to journal › Article
-
Mark
Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.
(
- Contribution to journal › Article
-
Mark
The environmental determinants of diabetes in the young (TEDDY) study: Study design
(
- Contribution to journal › Article
-
Mark
Variants in the FFAR1 Gene Are Associated with Beta Cell Function
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
-
Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle
(
- Contribution to journal › Article
- 2006
-
Mark
Authors' reply.
(
- Contribution to journal › Letter
-
Mark
Haplotype structures and large-scale association testing of the 5 ' AMP-activated protein kinase genes PRK4A2, PRKAB1, and PRK4B1 with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people
(
- Contribution to journal › Article
-
Mark
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
-
Mark
Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity
(
- Contribution to journal › Article
-
Mark
24-hour Ambulatory Blood Pressure is Linked to Chromosome 18q21-22 and Genetic Variation of NEDD4L Associates with Cross-Sectional and Longitudinal Blood Pressure in Swedes.
(
- Contribution to journal › Article
-
Mark
Common variants in MODY genes increase the risk of gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
(
- Contribution to journal › Article
-
Mark
The Kruppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people
(
- Contribution to journal › Article
-
Mark
Common variants in HNF-1 alpha and risk of type 2 diabetes.
(
- Contribution to journal › Article
- 2005
-
Mark
Association of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Diabetes-associated HLA genotypes affect birthweight in the general population.
(
- Contribution to journal › Article
-
Mark
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
(
- Contribution to journal › Article
-
Mark
Dipping and variability of blood pressure and heart rate at night are heritable traits.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people
(
- Contribution to journal › Article
-
Mark
Association testing of variants in the hepatocyte nuclear factor 4 alpha gene with risk of type 2 diabetes in 7,883 people
(
- Contribution to journal › Article
-
Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
(
- Contribution to journal › Article
-
Mark
Association of common variation in the HNF1 alpha gene region with risk of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Genetic and Nongenetic Regulation of CAPN10 mRNA Expression in Skeletal Muscle.
(
- Contribution to journal › Article
-
Mark
Genetic prediction of future type 2 diabetes
(
- Contribution to journal › Article
- 2004
-
Mark
Contribution of insulin-stimulated glucose uptake and basal hepatic insulin sensitivity to surrogate measures of insulin sensitivity.
(
- Contribution to journal › Article
-
Mark
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- Contribution to journal › Article
-
Mark
Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region.
(
- Contribution to journal › Article
-
Mark
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins.
(
- Contribution to journal › Article
-
Mark
The FOXC2 C-512T Polymorphism Is Associated with Obesity and Dyslipidemia.
(
- Contribution to journal › Article
- 2003
-
Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
-
Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity.
(
- Contribution to journal › Article
-
Mark
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
(
- Contribution to journal › Article
- 2002
-
Mark
A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
(
- Contribution to journal › Article
-
Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
- 2001
-
Mark
Characterization of the annexin I gene and evaluation of its role in type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes
(
- Contribution to journal › Article
-
Mark
The metabolic syndrome influences the risk of chronic complications in patients with type II diabetes
(
- Contribution to journal › Article
-
Mark
Cardiovascular morbidity and mortality associated with the metabolic syndrome
(
- Contribution to journal › Article
- 2000
-
Mark
The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of stroke
(
- Contribution to journal › Article
- 1999
-
Mark
A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene
(
- Contribution to journal › Article
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