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Literature DB >> 9802769

Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys)

K Kameoka, H Isotani, K Tanaka, H Kitaoka, N Ohsawa.

Abstract

Entities: Disease Mutation

Mesh：

Substances：

Year: 1998 PMID： 9802769 DOI： 10.2337/diacare.21.11.2034

Source DB: PubMed Journal: Diabetes Care ISSN： 0149-5992 Impact factor: 19.112

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7 in total

1. Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.

Authors: Belén Bornstein; José Antonio Mas; Clarice Patrono; Miguel Angel Fernández-Moreno; Emiliano González-Vioque; Yolanda Campos; Rosalba Carrozzo; Miguel Angel Martín; Pilar del Hoyo; Filippo M Santorelli; Joaquín Arenas; Rafael Garesse
Journal: Biochem J Date: 2005-05-01 Impact factor: 3.857

Review 2. Aminoacyl tRNA synthetases and their connections to disease.

Authors: Sang Gyu Park; Paul Schimmel; Sunghoon Kim
Journal: Proc Natl Acad Sci U S A Date: 2008-08-05 Impact factor: 11.205

Review 3. Mitochondrial diabetes mellitus.

Authors: J A Maassen; G M C Janssen; H H J P Lemkes
Journal: J Endocrinol Invest Date: 2002-05 Impact factor: 4.256

Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys)

1. Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.

Review 2. Aminoacyl tRNA synthetases and their connections to disease.

Review 3. Mitochondrial diabetes mellitus.

4. Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA ^Lys Gene.

Review 5. [Mitochondrial hearing impairment. Background, genetic predisposition and possibilities for diagnosis].

Review 6. Neurodegenerative disorders associated with diabetes mellitus.

Review 7. Endocrine disorders in mitochondrial disease.

Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys)

1. Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.

Review 2. Aminoacyl tRNA synthetases and their connections to disease.

Review 3. Mitochondrial diabetes mellitus.

4. Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA Lys Gene.

Review 5. [Mitochondrial hearing impairment. Background, genetic predisposition and possibilities for diagnosis].

Review 6. Neurodegenerative disorders associated with diabetes mellitus.

Review 7. Endocrine disorders in mitochondrial disease.

4. Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA ^Lys Gene.