✦ LIBER ✦

Associations between hyperglycaemia and somatic transversion mutations in mitochondrial DNA of people with diabetes mellitus

✍ Scribed by J. Kamiya; Y. Aoki

Publisher: Springer
Year: 2003
Tongue: English
Weight: 227 KB
Volume: 46
Category: Article
ISSN: 0012-186X
DOI: 10.1007/s00125-003-1215-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Heteroplasmy levels of a mitochondrial g

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

✍ Leen M. 't Hart; Janna J. Jansen; Herman H.P.J. Lemkes; Peter de Knijff; J. Anto 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 492 KB 👁 2 views

We showed previously that a mutation in the mitochondria1 tRNAL"(UUR' gene at position 3243 associates with maternally inherited diabetes and deafness (MIDD). This mutation shows heteroplasmy in DNA from peripheral blood and other tissues. To examine whether heteroplasmy levels in peripheral blood D

A pilot study of mitochondrial DNA point

A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance

✍ I. Martin-Kleiner; E. Pape-Medvidović; I. Pavlić-Renar; Ž. Metelko; R. Kušec; J. 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 172 KB

Association between M/L55-polymorphism o

Association between M/L55-polymorphism of paraoxonase enzyme and oxidative DNA damage in patients with type 2 diabetes mellitus and in control subjects

✍ R. Malin; V. Rantalaiho; X.-H. Huang; O. Wirta; A. Pasternack; J.S. Leinonen; H. 📂 Article 📅 1999 🏛 Springer 🌐 English ⚖ 22 KB

Absence of association between the Gly40

Absence of association between the Gly40→Ser mutation in the human glucagon receptor and Japanese patients with non-insulin-dependent diabetes mellitus or impaired glucose tolerance

✍ M. Odawara; Yoichi Tachi; Kamejiro Yamashita 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 43 KB