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定位澳大利亚牧羊犬的小脑退化症。

Mapping cerebellar abiotrophy in Australian Kelpies.

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Anim Genet. 2011 Dec;42(6):675-8. doi: 10.1111/j.1365-2052.2011.02199.x. Epub 2011 Apr 14.

Abstract

An autosomal recessive form of cerebellar abiotrophy occurs in Australian Kelpie dogs. Clinical signs range from mild ataxia with intention tremor to severe ataxia with seizures. A whole-genome mapping analysis was performed using Affymetrix Canine SNP array v2 on 11 affected and 19 control dogs, but there was no significant association with disease. A homozygosity analysis identified a three megabase region likely to contain the disease mutation. The region spans 29.8-33 Mb on chromosome 3, for which all affected dogs were homozygous for a common haplotype. Microsatellite markers were developed in the candidate region for linkage analysis that resulted in a logarithm of odds score suggestive of linkage. The candidate region contains 29 genes, none of which are known to cause ataxia.

摘要

小脑萎缩症的常染色体隐性形式发生在澳大利亚牧羊犬中。临床症状从轻微的意向性震颤共济失调到严重的癫痫共济失调不等。使用 Affymetrix Canine SNP 阵列 v2 在 11 只受影响的和 19 只对照犬上进行了全基因组图谱分析,但与疾病没有显著关联。纯合子分析确定了一个可能包含疾病突变的三个兆碱基区域。该区域跨越 3 号染色体上的 29.8-33 Mb,所有受影响的犬都为一个常见单倍型的纯合子。在候选区域开发了微卫星标记用于连锁分析,结果得出了连锁的可能性对数评分。候选区域包含 29 个基因,其中没有一个已知会导致共济失调。

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