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Mitochondrial DNA defects in diabetes mellitus.

作者信息

Alcolado J C

出版信息

Diabetologia. 1993 Jun;36(6):578-9. doi: 10.1007/BF02743279.

DOI:10.1007/BF02743279
PMID:8335184
Abstract
摘要

相似文献

1
Mitochondrial DNA defects in diabetes mellitus.糖尿病中的线粒体DNA缺陷。
Diabetologia. 1993 Jun;36(6):578-9. doi: 10.1007/BF02743279.
2
Mitochondrial diabetes mellitus: a review.线粒体糖尿病：综述
Biochim Biophys Acta. 1995 May 24;1271(1):253-60. doi: 10.1016/0925-4439(95)00036-4.
3
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.糖尿病是tRNALeu（UUR）基因中线粒体DNA点突变的异质表型特征之一。
FEBS Lett. 1993 Apr 26;321(2-3):194-6. doi: 10.1016/0014-5793(93)80106-5.
4
Prevalence of mitochondrial gene mutations in families with diabetes mellitus.糖尿病家族中线粒体基因突变的患病率。
Lancet. 1993 Dec 4;342(8884):1429-30. doi: 10.1016/0140-6736(93)92792-r.
5
Mitochondrial DNA [tRNA(Leu)(UUR)] mutation in a southern Italian diabetic population.
Diabetes Care. 1997 Apr;20(4):674-5. doi: 10.2337/diacare.20.4.674.
6
A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene.
Muscle Nerve Suppl. 1995;3:S137-41. doi: 10.1002/mus.880181427.
7
Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.线粒体糖尿病：日本患者中线粒体tRNA（Leu（UUR））基因突变所致糖尿病的患病率及临床特征
Diabetologia. 1994 May;37(5):504-10. doi: 10.1007/s001250050139.
8
Mitochondrial tRNA(Leu(UUR)) mutation at position 3243 detected in patients with type 1 diabetes.在1型糖尿病患者中检测到位于3243位的线粒体tRNA（亮氨酸（UUR））突变。
Diabetes Res Clin Pract. 2005 Jan;67(1):92-4. doi: 10.1016/j.diabres.2004.09.010.
9
Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.2型糖尿病中的线粒体基因变异：在中国一个家系中检测到与母系遗传糖尿病相关的新突变。
Chin Med J (Engl). 2000 Feb;113(2):111-6.
10
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.

引用本文的文献

1
Association between HLA and islet cell antibodies in diabetic patients with a mitochondrial DNA mutation at base pair 3243.
Diabetologia. 1996 Oct;39(10):1196-200. doi: 10.1007/BF02658506.

本文引用的文献

1
Importance of maternal history of non-insulin dependent diabetic patients.非胰岛素依赖型糖尿病患者的母亲病史的重要性。
BMJ. 1991 May 18;302(6786):1178-80. doi: 10.1136/bmj.302.6786.1178.
2
A rare mitochondrial DNA BstNI polymorphism in a family with type II diabetes.一个患有II型糖尿病的家族中罕见的线粒体DNA BstNI多态性
Nucleic Acids Res. 1991 Apr 25;19(8):1962. doi: 10.1093/nar/19.8.1962-a.
3
Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis.2型（非胰岛素依赖型）糖尿病：节俭表型假说。
Diabetologia. 1992 Jul;35(7):595-601. doi: 10.1007/BF00400248.
4
Nucleus-driven mutations of human mitochondrial DNA.人类线粒体DNA的核驱动突变。
J Inherit Metab Dis. 1992;15(4):456-71. doi: 10.1007/BF01799604.
5
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathy.肌阵挛性癫痫伴破碎红纤维（MERRF）脑病中异质性线粒体DNA突变的组织分离
Hum Genet. 1992 Nov;90(3):251-4. doi: 10.1007/BF00220072.
6
Does the mitochondrial DNA play a role in the pathogenesis of diabetes?
Diabetologia. 1992 Dec;35(12):1181-6. doi: 10.1007/BF00401375.
7
Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.一个患有母系遗传II型糖尿病和耳聋的大家系中线粒体tRNA(Leu)(UUR)基因的突变
Nat Genet. 1992 Aug;1(5):368-71. doi: 10.1038/ng0892-368.
8
Further evidence for a predominantly maternal transmission of maturity-onset type diabetes.
Endokrinologie. 1976 Oct;68(1):121-4.