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25 in total

1. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors: Y Goto; I Nonaka; S Horai
Journal: Nature Date: 1990-12-13 Impact factor: 49.962

2. Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination.

Authors: B Kruse; N Narasimhan; G Attardi
Journal: Cell Date: 1989-07-28 Impact factor: 41.582

3. Mitochondrial DNA mutations and survival rate.

Authors: T Ozawa; K Katsumata; M Hayakawa; M Yoneda; M Tanaka; S Sugiyama
Journal: Lancet Date: 1995-01-21 Impact factor: 79.321

4. Human diabetes associated with a mutation in the tyrosine kinase domain of the insulin receptor.

Authors: M Odawara; T Kadowaki; R Yamamoto; Y Shibasaki; K Tobe; D Accili; C Bevins; Y Mikami; N Matsuura; Y Akanuma
Journal: Science Date: 1989-07-07 Impact factor: 47.728

5. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

Authors: A M Remes; K Majamaa; R Herva; I E Hassinen
Journal: Neurology Date: 1993-05 Impact factor: 9.910

6. Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene.

Authors: M Odawara; K Sasaki; K Yamashita
Journal: J Clin Endocrinol Metab Date: 1995-04 Impact factor: 5.958

7. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.

Authors: M Kishimoto; M Hashiramoto; S Araki; Y Ishida; T Kazumi; E Kanda; M Kasuga
Journal: Diabetologia Date: 1995-02 Impact factor: 10.122

8. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.

Authors: H Katagiri; T Asano; H Ishihara; K Inukai; M Anai; T Yamanouchi; K Tsukuda; M Kikuchi; H Kitaoka; N Ohsawa
Journal: Diabetologia Date: 1994-05 Impact factor: 10.122

9. Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.

Authors: M P King; Y Koga; M Davidson; E A Schon
Journal: Mol Cell Biol Date: 1992-02 Impact factor: 4.272

10. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.

Authors: J M van den Ouweland; H H Lemkes; R C Trembath; R Ross; G Velho; D Cohen; P Froguel; J A Maassen
Journal: Diabetes Date: 1994-06 Impact factor: 9.461