精神分裂症患者与健康人群中SCA1、MJD/SCA3、HD、SBMA、DRPLA、MD、FRAXA和FRDA基因中三联体数量的比较。 - Suppr

Suppr

超能文献

Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population.

作者信息

Culjković B, Stojković O, Savić D, Zamurović N, Nesić M, Major T, Romac S, Vukosavić S

出版信息

Am J Med Genet. 2000 Dec 4;96(6):884-7. doi: 10.1002/1096-8628(20001204)96:6<884::aid-ajmg41>3.0.co;2-m.

DOI:10.1002/1096-8628(20001204)96:6<884::aid-ajmg41>3.0.co;2-m

PMID:11121205

Abstract

摘要

相似文献

Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population.

Am J Med Genet. 2000 Dec 4;96(6):884-7. doi: 10.1002/1096-8628(20001204)96:6<884::aid-ajmg41>3.0.co;2-m.

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.

Arch Neurol. 2000 Apr;57(4):540-4. doi: 10.1001/archneur.57.4.540.

The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls.

J Neurogenet. 2000 Dec;14(4):257-63. doi: 10.3109/01677060009084502.

Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?

Psychiatr Genet. 2001 Dec;11(4):201-5. doi: 10.1097/00041444-200112000-00004.

[Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):83-5.

[SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].

Zhonghua Yi Xue Za Zhi. 1997 Nov;77(11):819-22.

[New insights in the molecular genetics and pathophysiology of hereditary ataxias].

Nervenarzt. 1999 Jun;70(6):491-5. doi: 10.1007/s001150050470.

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.

Am J Med Genet. 2002 Jul 8;114(5):578-83. doi: 10.1002/ajmg.10514.

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.

Hum Genet. 1999 Jun;104(6):516-22. doi: 10.1007/s004390050997.

Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich's ataxia.

J Mol Biol. 2000 Oct 6;302(5):1063-80. doi: 10.1006/jmbi.2000.4073.

引用本文的文献

Loss of Ataxin-1 Potentiates Alzheimer's Pathogenesis by Elevating Cerebral BACE1 Transcription.

Cell. 2019 Aug 22;178(5):1159-1175.e17. doi: 10.1016/j.cell.2019.07.043.

Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?

Cell Mol Life Sci. 2014 Dec;71(23):4519-44. doi: 10.1007/s00018-014-1717-x. Epub 2014 Sep 20.

A genome-wide quantitative linkage scan of niacin skin flush response in families with schizophrenia.

Schizophr Bull. 2013 Jan;39(1):68-76. doi: 10.1093/schbul/sbr054. Epub 2011 Jun 7.

Genomic and epigenomic instability, fragile sites, schizophrenia and autism.

Curr Genomics. 2010 Sep;11(6):447-69. doi: 10.2174/138920210793176001.

Anticipation and CAG*CTG repeat expansion in schizophrenia and bipolar affective disorder.

Curr Psychiatry Rep. 2003 Jun;5(2):145-54. doi: 10.1007/s11920-003-0031-3.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验