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A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

作者信息

Mills K A, Sunada Y, Campbell K P, Mathews K D

机构信息

Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City 52242, USA.

出版信息

Mamm Genome. 1995 Sep;6(9):664-5. doi: 10.1007/BF00352377.

DOI:10.1007/BF00352377
PMID:8535078
Abstract
摘要

相似文献

1
A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.
Mamm Genome. 1995 Sep;6(9):664-5. doi: 10.1007/BF00352377.
2
Analyses of beta-1 syntrophin, syndecan 2 and gem GTPase as candidates for chicken muscular dystrophy.对β-1 肌养蛋白、多配体聚糖-2和宝石GTP酶作为鸡肌肉萎缩症候选因素的分析。
Exp Anim. 2003 Oct;52(5):391-6. doi: 10.1538/expanim.52.391.
3
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
Mamm Genome. 1997 Jun;8(6):394-8. doi: 10.1007/s003359900454.
4
The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.mdx小鼠肌营养不良的分子基础：一个点突变。
Science. 1989 Jun 30;244(4912):1578-80. doi: 10.1126/science.2662404.
5
The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.人类面肩肱型肌营养不良症的分子遗传学及肌营养不良小鼠模型
Curr Opin Neurol. 1996 Oct;9(5):394-9.
6
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
Muscle Nerve Suppl. 1995;2:S98-102.
7
The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
Genomics. 1998 Apr 1;49(1):129-32. doi: 10.1006/geno.1997.5208.
8
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.小鼠肌营养不良（myd）突变：在与人类4号染色体长臂远端同源的区间内进行精细定位。
Muscle Nerve Suppl. 1995(2):S98-102.
9
Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2.小鼠肌联蛋白基因的染色体定位及其与2号染色体上“伴肌炎的肌营养不良症”和伴肌动蛋白基因的关系。
Genomics. 1993 Dec;18(3):559-61. doi: 10.1016/s0888-7543(05)80356-8.
10
C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice.C 端截短的微小抗肌萎缩蛋白将肌萎缩蛋白结合蛋白和肌营养不良蛋白聚糖复合物招募到抗肌萎缩蛋白相关糖蛋白复合物中，并减轻有症状的泛素/抗肌萎缩蛋白双敲除小鼠的肌肉萎缩。
Mol Ther. 2006 Jul;14(1):79-87. doi: 10.1016/j.ymthe.2006.01.007. Epub 2006 Mar 23.

本文引用的文献

1
Heterogeneity of dystrophin-associated proteins.
J Biochem. 1993 Jul;114(1):132-9. doi: 10.1093/oxfordjournals.jbchem.a124128.
2
A Macintosh program for storage and analysis of experimental genetic mapping data.一个用于存储和分析实验性基因图谱数据的麦金塔程序。
Mamm Genome. 1993;4(6):303-13. doi: 10.1007/BF00357089.
3
Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.人类碱性A1的克隆，一种定位于8号染色体q23 - 24区域编码的独特59 kDa抗肌萎缩蛋白相关蛋白。
Proc Natl Acad Sci U S A. 1994 May 10;91(10):4446-50. doi: 10.1073/pnas.91.10.4446.
4
Heterogeneity of the 59-kDa dystrophin-associated protein revealed by cDNA cloning and expression.通过cDNA克隆和表达揭示的59-kDa抗肌萎缩蛋白相关蛋白的异质性
J Biol Chem. 1994 Feb 25;269(8):6040-4.
5
A mouse monochromosome 8 somatic cell hybrid: a reagent for chromosome 8 isolation.一种小鼠8号单染色体体细胞杂种：用于分离8号染色体的试剂。
Mamm Genome. 1994 Sep;5(9):572-3. doi: 10.1007/BF00354932.
6
A genetic map of the mouse with 4,006 simple sequence length polymorphisms.一张具有4006个简单序列长度多态性的小鼠遗传图谱。
Nat Genet. 1994 Jun;7(2 Spec No):220-45. doi: 10.1038/ng0694supp-220.
7
The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.
Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551.
8
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.三种肌肉萎缩症：细胞骨架与细胞外基质连接的丧失。
Cell. 1995 Mar 10;80(5):675-9. doi: 10.1016/0092-8674(95)90344-5.
9
Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.小鼠肌养蛋白有两种形式，一种分子量为58kd的与肌营养不良蛋白相关的蛋白质，它们在一级结构和组织分布上有所不同。
Neuron. 1993 Sep;11(3):531-40. doi: 10.1016/0896-6273(93)90157-m.
10
Genetic mapping near the myd locus on mouse chromosome 8.小鼠8号染色体上myd基因座附近的遗传图谱。
Mamm Genome. 1995 Apr;6(4):278-80. doi: 10.1007/BF00352416.