Chromosomal Mapping of the Peroneal Muscular Atrophy (pma) Gene in the Mouse

Hideki KATOH; Yuka WATANABE; Michi EBUKURO; Kaori MUGURUMA; Shuji TAKABAYASHI; Toshihiko SHIROISHI

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Chromosomal Mapping of the Peroneal Muscular Atrophy (pma) Gene in the Mouse

机译：小鼠腓总肌萎缩（pma）基因的染色体作图

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摘要

We conducted chromosomal mapping of the pma gene that is a causative gene in the peroneal muscular atrophy mouse, which shows a club foot at birth and unusual gait due to a dropped foot in the adult. Linkage analyses using backcross progeny revealed a significant linkage between the pma gene and three microsatellite markers, D5Mit263 at 73 cM, D5Mit141 and D5Mit97 at 74 cM on Chr 5, The gene order was determined as follows: centromere-D5Mit263-[2.65 cM]-D5Mit141-[2.56 cM]-pma-[5.13 cM]-D5Mit97-telomere.

机译：我们对腓骨肌萎缩症小鼠中的致病基因pma基因进行了染色体作图，该基因显示了出生时的俱乐部脚和成年人脚掉下的步态。使用回交子代的连锁分析显示，pma基因与三个微卫星标记之间的显着关联，即在Chr 5上为73 cM的D5Mit263、74 cM的D5Mit141和D5Mit97，基因顺序确定如下：centromere-D5Mit263- [2.65 cM]- D5Mit141- [2.56 cM] -pma- [5.13 cM] -D5Mit97-端粒。

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来源
《Experimental Animals》 |2003年第5期|p.433-436|共4页
作者
Hideki KATOH; Yuka WATANABE; Michi EBUKURO; Kaori MUGURUMA; Shuji TAKABAYASHI; Toshihiko SHIROISHI;
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作者单位

Institute for Experimental Animals, Hamamatsu University School of Medicine, 1-20-1 Handayama Hamamatsu Shizuoka 431-3192, Japan;

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收录信息美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
原文格式 PDF
正文语种 eng
中图分类动物学;
关键词
chr 5; mouse; peroneal muscular atrophy;

机译：5小时;小鼠;腓肠肌萎缩;

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1. The developmental and genetic basis of 'clubfoot' in the peroneal muscular atrophy mutant mouse [J] . Collinson J. Martin, Lindstrom Nils O., Neves Carlos, Development . 2018,第3期

机译：“Clubfoot”在肌腱萎缩突变小鼠中的发育和遗传基础
2. Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families. [J] . Viollet L, Zarhrate M, Maystadt I, European journal of human genetics: EJHG . 2004,第6期

机译：改良的常染色体隐性遗传性慢性远端脊髓远端肌肉萎缩症到11q13.3染色体的遗传作图以及欧洲家庭中连锁不平衡的证据。
3. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. [J] . McEntagart M, Bell C, Donaghy M, Journal of Neurology, Neurosurgery and Psychiatry . 2002,第6期

机译：伴有声带无力的腓肌萎缩的临床和遗传异质性。
4. Mutations in the mouse Lmna gene causing progeria, muscular dystrophy and cardiomyopathy [C] . Serguei Kozlov, Leslie Mounkes, Dedra Cutler, Novartis Foundation symposium on Nuclear organization in development and disease . 2005

机译：小鼠LMNA基因中的突变导致普鲁比亚，肌肉营养不良和心肌病
5. Characterizing the effect of mutations within exon 7 of the murine survival motor neuron gene to model spinal muscular atrophy in the mouse. [D] . Hammond, Suzan Michelle. 2010

机译：表征小鼠存活运动神经元基因外显子7内突变对小鼠脊髓性肌萎缩模型的影响。
6. The developmental and genetic basis of ‘clubfoot’ in the peroneal muscular atrophy mutant mouse [O] . J. Martin Collinson, Nils O. Lindström, Carlos Neves, -1

机译：腓骨肌萎缩突变小鼠中马蹄内翻足的发育和遗传基础
7. Chromosomal Mapping of the Peroneal Muscular Atrophy (pma) Gene in the Mouse [O] . Katoh, Hideki, Watanabe, Yuka, Ebukuro, Michi, 2003

机译：小鼠腓总肌萎缩（pma）基因的染色体作图

Chromosomal Mapping of the Peroneal Muscular Atrophy (pma) Gene in the Mouse

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