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Maturity onset diabetes of the young (MODY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locus.

作者信息

Shield J, Owen K, Robinson D O, Mackay D, Ellard S, Hattersley A, Temple I K

出版信息

Diabetologia. 2001 Jul;44(7):924. doi: 10.1007/s001250100557.

DOI:10.1007/s001250100557
PMID:11508282
Abstract
摘要

相似文献

1
Maturity onset diabetes of the young (MODY) and early onset Type II diabetes are not caused by loss of imprinting at the transient neonatal diabetes (TNDM) locus.
Diabetologia. 2001 Jul;44(7):924. doi: 10.1007/s001250100557.
2
Neonatal diabetes mellitus: a disease linked to multiple mechanisms.新生儿糖尿病：一种与多种机制相关的疾病。
Orphanet J Rare Dis. 2007 Mar 9;2:12. doi: 10.1186/1750-1172-2-12.
3
Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus.短暂性新生儿糖尿病患者中TNDM基因座和贝克威思-维德曼综合征着丝粒基因座的表型改变
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4
Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach.评估2型糖尿病中短暂性新生儿糖尿病（TNDM）区域常见基因变异的作用：一种比较基因组学和标签单核苷酸多态性方法。
Diabetes. 2006 Aug;55(8):2272-6. doi: 10.2337/db06-0216.
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Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes.与已知青年发病的成年型糖尿病（MODY）基因无关的早发型常染色体显性2型糖尿病的表型特征。
Diabetes Care. 1999 Feb;22(2):253-61. doi: 10.2337/diacare.22.2.253.
6
Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.6q24染色体异常作为早发、非肥胖、非自身免疫性糖尿病且无新生儿糖尿病病史的病因
Diabet Med. 2015 Jul;32(7):963-7. doi: 10.1111/dme.12758. Epub 2015 Apr 11.
7
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23.定位于6号染色体q22-q23区域的新生儿糖尿病印迹基因的进一步证据。
Hum Mol Genet. 1996 Aug;5(8):1117-21. doi: 10.1093/hmg/5.8.1117.
8
Mutations in the genes for hepatocyte nuclear factor (HNF)-1alpha, -4alpha, -1beta, and -3beta; the dimerization cofactor of HNF-1; and insulin promoter factor 1 are not common causes of early-onset type 2 diabetes in Pima Indians.肝细胞细胞核因子（HNF）-1α、-4α、-1β和-3β基因；HNF-1的二聚化辅助因子；以及胰岛素启动因子1的突变并非皮马印第安人早发型2型糖尿病的常见病因。
Diabetes Care. 2000 Mar;23(3):302-4. doi: 10.2337/diacare.23.3.302.
9
Association of novel variants in the hepatocyte nuclear factor 4A gene with maturity onset diabetes of the young and early onset type 2 diabetes.肝细胞核因子 4A 基因中新变异与青年发病的成年型糖尿病及早发 2 型糖尿病的关联。
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Mutations of maturity-onset diabetes of the young (MODY) genes in Thais with early-onset type 2 diabetes mellitus.泰国早发型2型糖尿病患者中年轻的成年发病型糖尿病（MODY）基因突变情况。
Clin Endocrinol (Oxf). 2009 Jun;70(6):847-53. doi: 10.1111/j.1365-2265.2008.03397.x. Epub 2008 Sep 22.

引用本文的文献

1
Transient neonatal diabetes mellitus in an extremely preterm infant.一名极早产儿的短暂性新生儿糖尿病
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.11.2008.1185. Epub 2009 May 8.
2
Data-mining analysis suggests an epigenetic pathogenesis for type 2 diabetes.数据挖掘分析表明2型糖尿病存在表观遗传发病机制。
J Biomed Biotechnol. 2005 Jun 30;2005(2):104-12. doi: 10.1155/JBB.2005.104.
3
Diabetic ketoacidosis and hyperglycemic hyperosmolar syndrome after renal transplantation in the United States.美国肾移植术后的糖尿病酮症酸中毒和高血糖高渗综合征
BMC Endocr Disord. 2003 Mar 24;3(1):1. doi: 10.1186/1472-6823-3-1.
4
Transient neonatal diabetes, a disorder of imprinting.短暂性新生儿糖尿病，一种印记障碍。
J Med Genet. 2002 Dec;39(12):872-5. doi: 10.1136/jmg.39.12.872.