Polymorphisms of the human hexokinase II gene: lack of association with NIDDM and insulin resistance
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Point mutations in the HK-II gene found in type 2 diabetes are not close to glucose and ATP binding sites and are not associated with insulin resistance.
“Several groups have looked for point mutations in the HK-II gene in individuals with type 2 diabetes, and, although several nucleotide substitutions have been found, none are close to the glucose and ATP binding sites and none have been associated with insulin resistance [203–205].”
From Pathogenesis of insulin resistance in skeletal muscle (2010) · cites this paper as [204]
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References 23 · Cited by 22
- Authors
- Laakso, M., Malkki, M., Kek�l�inen, P., Kuusisto, J., & Deeb, S. S.
- Affiliations
- University of Washington (US)
- University of Eastern Finland (FI)
- Venue
- Diabetologia
- Published
- 1995-04-01
- Volume
- 38
- Issue
- 5
- Pages
- 617-622
- ISSN
- 0012-186X (ISSN-L)
- 1432-0428
- OpenAlex
- W2040827324
- Cited by
- 22
- References
- 23
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 1 · 2018: 2 · 2015: 1 · 2013: 2
- FWCI
- 0.83
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Diabetologia (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Academy of Finland
- Medical Research Council
- National Heart, Lung, and Blood Institute (P01HL030086, HL3-0086)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- hexokinase 2, type 2 diabetes, insulin resistance, candidate gene association, skeletal muscle, adipose tissue, Finnish population
- MeSH terms
- Adipose Tissue, Alleles, Base Sequence, Blood Glucose, Diabetes Mellitus, Type 2, Exons, Female, Finland, Hexokinase, Homozygote, Humans, Insulin Resistance, Isoenzymes, Male, Middle Aged, Molecular Sequence Data, Polymorphism, Genetic, Reference Values, Polymorphism, Restriction Fragment Length, Glucose Clamp Technique, Point Mutation, DNA Primers, Muscle, Skeletal
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