Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients

机译：特发性少精子症患者脊髓小脑共济失调1型（SCA1）基因中CAG重复序列的扩增

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摘要

PurposeThe lengths of CAG repeats in two spinocerebellar ataxia genes, SCA1 and SCA3, were analyzed to determine whether such repeats exist in higher numbers in infertile males.

机译：目的分析两个脊髓小脑共济失调基因SCA1和SCA3中CAG重复序列的长度，以确定在不育男性中这种重复序列是否以更高的数量存在。

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期刊名称 Journal of Assisted Reproduction and Genetics
作者
Yen-Chein Lai; Wen-Chung Wang; Jiann-Jou Yang; Shuan-Yow Li;
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作者单位

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年(卷),期 2009(26),5
年度 2009
页码 257–261
总页数 5
原文格式 PDF
正文语种
中图分类遗传学;妇产科学;
关键词
CAG repeats Oligozoospermia Spinocerebellar ataxia type 1 gene Spinocerebellar ataxia type 3 gene;

机译：CAG重复;少精症;脊髓小脑共济失调1型基因;脊髓小脑共济失调3型基因;

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专利

1. Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients [J] . Yen-Chein Lai, Wen-Chung Wang, Jiann-Jou Yang, Journal of Assisted Reproduction and Genetics . 2009,第5期

机译：特发性少精子症患者脊髓小脑共济失调1型（SCA1）基因中CAG重复序列的扩增
2. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India. [J] . Basu P, Chattopadhyay B, Gangopadhaya PK, Human Genetics . 2000,第6期

机译：分析脊髓小脑性共济失调患者的SCA1，SCA2，SCA3，SCA6，SCA7和DRPLA基因座中的CAG重复序列，以及印度东部9个种族人群中SCA1，SCA2和SCA6基因座上CAG重复序列的分布。
3. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? [J] . Savic D, Topisirovic I, Keckarevic M, Psychiatric genetics . 2001,第4期

机译：脊髓小脑性共济失调1（SCA1）基因位点的31个CAG重复等位基因是否与三核苷酸扩增疾病非特异性相关？
4. Role of EMG Rectification for Corticomuscular and Intermuscular Coherence Estimation of Spinocerebellar Ataxia Type 2 (SCA2) [C] . Y. Ruiz-Gonzalez, L. Velazquez-Perez, R. Rodriguez-Labrada, Iberoamerican congress on pattern recognition . 2019

机译：EMG矫正对2型脊髓小脑共济失调（SCA2）的皮质肌和肌间相干估计的作用。
5. Infant Onset Spinocerebellar Ataxia Type 13 Mutation Leads to Developmental and Rapid Degenerative Phenotypes Related to Hyperexcitability in Purkinje Cells [D] . Ulrich, Brittany Nicole. 2017

机译：婴儿起病的脊髓小脑共济失调13型突变导致发展和快速退化的表型与浦肯野细胞过度兴奋有关。
6. Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2 [O] . Tua Vinther-Jensen, Jakob Ek, Morten Duno, 2013

机译：胚系CAG重复不稳定性会导致CAG重复严重扩增并伴发2型小儿发作性小脑共济失调
7. Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients [O] . Yen-Chein Lai 2011

机译：特发性少精子症患者脊髓小脑性共济失调1型（sCa1）基因CaG重复序列的扩增

Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients

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