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- 2004
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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
- 2003
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Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
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Mark
Effects of common polymorphisms in the alpha(1A)-, alpha(2B)-, beta(1)- and beta(2)-adrenoreceptors on haemodynamic responses to adrenaline
(
- Contribution to journal › Article
-
Mark
The insertion/deletion variation in the alpha2B-adrenoceptor does not seem to modify the risk for acute myocardial infarction, but may modify the risk for hypertension in sib-pairs from families with type 2 diabetes
(
- Contribution to journal › Article
- 2002
-
Mark
Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.
(
- Contribution to journal › Article
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Mark
Polymorphism in the Calpain 10 gene influences glucose metabolism in human fat cells
(
- Contribution to journal › Article
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Mark
Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: Report of three new mutations
(
- Contribution to journal › Article
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Mark
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
(
- Contribution to journal › Article
- 2001
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Mark
Common variants in the beta2-(Gln27Glu) and beta3-(Trp64Arg)--adrenoceptor genes are associated with elevated serum NEFA concentrations and type II diabetes
(
- Contribution to journal › Article