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Exclusion of two candidate genes, Spnb-2 and Dcd, for the wobbler spinal muscular atrophy gene on proximal mouse chromosome 11.

作者信息

Lengeling A, Zimmer W E, Goodman S R, Ma Y, Bloom M L, Bruneau G, Krieger M, Thibault J, Kaupmann K, Jockusch H

机构信息

University of Bielefeld, Developmental Biology Unit, Germany.

出版信息

Mamm Genome. 1994 Mar;5(3):163-6. doi: 10.1007/BF00352348.

DOI:10.1007/BF00352348
PMID:8199405
Abstract
摘要

相似文献

1
Exclusion of two candidate genes, Spnb-2 and Dcd, for the wobbler spinal muscular atrophy gene on proximal mouse chromosome 11.
Mamm Genome. 1994 Mar;5(3):163-6. doi: 10.1007/BF00352348.
2
YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.小鼠近端11号染色体上Rab1和摆动(wr)型脊髓性肌萎缩症基因区域的酵母人工染色体(YAC)重叠群,以及人类2号染色体上的同源区域。
Genomics. 1996 Mar 15;32(3):447-54. doi: 10.1006/geno.1996.0140.
3
The gene for cytoplasmatic malate dehydrogenase, Mor2, is closely linked to the wobbler spinal muscular atrophy gene (wr).
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4
Spinal muscular atrophy gene wobbler of the mouse: evidence from chimeric spinal cord and testis for cell-autonomous function.
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Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p.一种以上肢为主的远端型脊髓性肌萎缩症在7号染色体短臂上的定位。
Hum Mol Genet. 1995 Sep;4(9):1629-32. doi: 10.1093/hmg/4.9.1629.
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A candidate gene for X-linked spinal muscular atrophy.X连锁脊髓性肌萎缩症的一个候选基因。
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Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.常染色体隐性慢性远端脊髓性肌萎缩症定位于11号染色体q13区域。
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X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.X连锁远端遗传性运动神经病定位于X染色体q13.1-q21的DSMAX基因座。
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Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.常染色体隐性遗传性脊髓性肌萎缩症5q13染色体上候选基因的分子分析:未患病个体中SMN基因纯合缺失的证据。
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No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.
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引用本文的文献

1
The gene for cytoplasmatic malate dehydrogenase, Mor2, is closely linked to the wobbler spinal muscular atrophy gene (wr).
Mamm Genome. 1996 Mar;7(3):250. doi: 10.1007/s003359900280.

本文引用的文献

1
The Gene for Ciliary Neurotrophic Factor (CNTF) Maps to Murine Chromosome 19 and its Expression is Not Affected in the Hereditary Motoneuron Disease 'Wobbler' of the Mouse.睫状神经营养因子(CNTF)基因定位于小鼠第19号染色体,且其表达在小鼠遗传性运动神经元疾病“摇摆病”中不受影响。
Eur J Neurosci. 1991 Oct;3(11):1182-1186. doi: 10.1111/j.1460-9568.1991.tb00052.x.
2
Erythroid and nonerythroid spectrins.红细胞和非红细胞血影蛋白
Blood. 1993 Jun 15;81(12):3173-85.
3
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
铜锌超氧化物歧化酶基因突变与家族性肌萎缩侧索硬化症相关。
Nature. 1993 Mar 4;362(6415):59-62. doi: 10.1038/362059a0.
4
mnd2: a new mouse model of inherited motor neuron disease.
Genomics. 1993 Jun;16(3):669-77. doi: 10.1006/geno.1993.1246.
5
Sperm tail axoneme alterations in the Wobbler mouse.
J Reprod Fertil. 1980 Jan;58(1):267-70. doi: 10.1530/jrf.0.0580267.
6
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
7
An hereditary motor neurone disease with progressive denervation of muscle in the mouse: the mutant 'wobbler'.一种遗传性运动神经元疾病,小鼠中存在肌肉进行性失神经支配:突变型“蹒跚者”。
J Neurol Neurosurg Psychiatry. 1968 Dec;31(6):535-42. doi: 10.1136/jnnp.31.6.535.
8
Studies on a murine form of spontaneous lower motor neuron degeneration--the wobbler (wa) mouse.关于一种小鼠自发性下运动神经元变性形式——摇摆(wa)小鼠的研究。
Am J Pathol. 1974 Jul;76(1):63-78.
9
Developmental and transformation-sensitive expression of the Sparc gene on mouse chromosome 11.小鼠11号染色体上Sparc基因的发育及转化敏感性表达
EMBO J. 1986 Aug;5(8):1831-7. doi: 10.1002/j.1460-2075.1986.tb04434.x.
10
Motoneuron loss in the abducens nucleus of wobbler mice.摇摆小鼠展神经核中的运动神经元损失。
Brain Res. 1987 Feb 24;404(1-2):127-32. doi: 10.1016/0006-8993(87)91363-1.