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Diabetes Research and Clinical Practice
Volume 75, Issue 1
, Pages 27-29
, January 2007
A patient with Werner syndrome and adiponectin gene mutation
References
- . Genetic syndromes in man with potential relevance to the pathophysiology of aging. Birth Defects Orig. Artic. Ser. 1978;14:5–39
- . Clinical characteristics of Werner syndrome and other premature aging syndromes: pattern of aging in progeroid syndrome. In: Goto M, Miller RW editor. In From Premature Gray Hair to Helicase-Werner Syndrome: Implication for Aging and Cancer. Basel: Karger; 2001;p. 27–39
- Positional cloning of the Werner's syndrome gene. Science. 1996;272:258–262
- Mutation and haplotype analysis of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese populations. Hum. Genet. 1997;100:123–130
- . Dysadipocytokinemia in Werner syndrome and its recovery by treatment with pioglitazone. Diabetes Care (Lett.). 2004;27:2562–2563
- Association of adiponectin mutation with type 2 diabetes: a candidate gene for the insulin resistance syndrome. Diabetes. 2002;51:2325–2328
- Impaired multimerization of human adiponectin mutant associated with diabetes. J. Biol. Chem. 2003;278:40352–40363
- Disturbed secretion of mutant adiponectin associated with the metabolic syndrome. Biochem. Biophys. Res. Commun. 2003;306:286–292
PII: S0168-8227(06)00224-5
doi: 10.1016/j.diabres.2006.05.010
© 2006 Elsevier Ireland Ltd. All rights reserved.
« Previous
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Diabetes Research and Clinical Practice
Volume 75, Issue 1
, Pages 27-29
, January 2007
