线粒体基因突变与糖尿病 - Suppr

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超能文献

Mitochondrial gene mutations and diabetes mellitus.

作者信息

Sue C M, Holmes-Walker D J, Morris J G, Boyages S C, Crimmins D S, Byrne E

出版信息

Lancet. 1993 Feb 13;341(8842):437-8. doi: 10.1016/0140-6736(93)93032-v.

DOI:10.1016/0140-6736(93)93032-v

PMID:7679179

Abstract

摘要

相似文献

Mitochondrial gene mutations and diabetes mellitus.线粒体基因突变与糖尿病

Lancet. 1993 Feb 13;341(8842):437-8. doi: 10.1016/0140-6736(93)93032-v.

Mitochondrial gene mutations and diabetes mellitus.线粒体基因突变与糖尿病

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Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review.与线粒体DNA T14709C点突变相关的早发性糖尿病：病例报告及文献综述

J Pediatr Endocrinol Metab. 1999 Mar-Apr;12(2):207-13. doi: 10.1515/jpem.1999.12.2.207.

Mitochondrial medicine.线粒体医学

QJM. 1997 Nov;90(11):657-67. doi: 10.1093/qjmed/90.11.657.

Mitochondrial 3243 BP mutation: a case report.线粒体3243碱基对突变：一例报告

Diabetes Nutr Metab. 2001 Dec;14(6):343-8.

Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene.线粒体tRNA（Leu（UUR））基因A3243G突变的异质性表现

Arch Dis Child. 2000 May;82(5):407-11. doi: 10.1136/adc.82.5.407.

[Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].[线粒体脑肌病家族中糖尿病的临床特征]

Nihon Rinsho. 1994 Oct;52(10):2606-10.

Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus.与糖尿病相关的母系遗传的线粒体DNA部分直接串联重复。

Hum Mol Genet. 1993 Oct;2(10):1619-24. doi: 10.1093/hmg/2.10.1619.

Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.在一个因线粒体tRNA（亮氨酸（UUR））基因突变导致母系遗传糖尿病和耳聋的家族中，胰岛素对葡萄糖的分泌反应减弱，但胰岛素和胰高血糖素对精氨酸的分泌反应正常。

Diabetes Care. 2001 Jul;24(7):1253-8. doi: 10.2337/diacare.24.7.1253.

GAD antibody in mitochondrial diabetes associated with tRNA(UUR) mutation at position 3271.与3271位tRNA（UUR）突变相关的线粒体糖尿病中的谷氨酸脱羧酶抗体。

Diabetes Care. 2002 Jun;25(6):1097-8. doi: 10.2337/diacare.25.6.1097.

引用本文的文献

Medical care from childhood to adulthood in type 1 and type 2 diabetes.1型和2型糖尿病患者从儿童期到成年期的医疗护理。

J Endocrinol Invest. 2001 Oct;24(9):692-707. doi: 10.1007/BF03343914.

Are MELAS and diabetes mellitus caused solely by the same mutation at np 3243 of the mitochondrial gene?线粒体基因第3243位核苷酸处的相同突变是导致线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）及糖尿病的唯一原因吗？

Diabetologia. 1995 Dec;38(12):1488-90. doi: 10.1007/BF00400616.

Maternally inherited diabetes and deafness: a new diabetes subtype.母系遗传的糖尿病和耳聋：一种新的糖尿病亚型。

Diabetologia. 1996 Apr;39(4):375-82. doi: 10.1007/BF00400668.

Mitochondrial gene defects in patients with NIDDM.非胰岛素依赖型糖尿病患者的线粒体基因缺陷

Diabetologia. 1994 Apr;37(4):372-6. doi: 10.1007/BF00408473.

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).与tRNA（亮氨酸（UUR））基因线粒体点突变相关的胰腺β细胞分泌缺陷：对七个患有线粒体脑肌病、乳酸酸中毒和卒中样发作（MELAS）家庭的研究

Diabetologia. 1994 Aug;37(8):818-25. doi: 10.1007/BF00404339.

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