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Evidence for allelism of leaner and tottering in the mouse.

作者信息

Tsuji S, Meier H

出版信息

Genet Res. 1971 Feb;17(1):83-8. doi: 10.1017/s0016672300012040.

DOI:10.1017/s0016672300012040
PMID:4933322
Abstract
摘要

相似文献

1
Evidence for allelism of leaner and tottering in the mouse.
Genet Res. 1971 Feb;17(1):83-8. doi: 10.1017/s0016672300012040.
2
Linkage of serum esterase and tottering in the mouse.
J Hered. 1969 Jul-Aug;60(4):221-2. doi: 10.1093/oxfordjournals.jhered.a107976.
3
Myodystrophy, a new myopathy on chromosome 8 of the mouse.肌营养不良症,小鼠8号染色体上的一种新型肌病。
J Hered. 1976 May-Jun;67(3):135-8. doi: 10.1093/oxfordjournals.jhered.a108687.
4
[Genetic relationship of two mutant genes which producing three different syndromes in the mouse (author's transl)].在小鼠中产生三种不同综合征的两个突变基因的遗传关系(作者译)
Jikken Dobutsu. 1975 Jul;24(3):111-8. doi: 10.1538/expanim1957.24.3_111.
5
Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby.三种导致小鼠不成比例侏儒症的隐性突变:软骨发育不全、短体型和短粗型。
J Hered. 1968 Sep-Oct;59(5):300-8. doi: 10.1093/oxfordjournals.jhered.a107725.
6
Three syndromes produced by two mutant genes in the mouse. Clinical, pathological, and ultrastructural bases of tottering, leaner, and heterozygous mice.
J Hered. 1971 Sep-Oct;62(5):297-302. doi: 10.1093/oxfordjournals.jhered.a108176.
7
Genetic study of osteopetrosis in the Norway rat.挪威大鼠骨硬化症的遗传学研究。
J Hered. 1974 Nov-Dec;65(6):373-5. doi: 10.1093/oxfordjournals.jhered.a108554.
8
Cataract--webbed Peromyscus. I. Genetics of cataract in P. maniculatus.
J Hered. 1979 Jan-Feb;70(1):27-30. doi: 10.1093/oxfordjournals.jhered.a109183.
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Breeding results of rabbits with familial hypercholesterolemia: effects of age and sex on serum lipids.家族性高胆固醇血症家兔的繁殖结果:年龄和性别对血脂的影响。
Z Versuchstierkd. 1984;26(2):61-6.
10
Disturbances in developmental pathways leading to a neurological disorder of genetic origin, "leaner", in mice.导致小鼠出现遗传性神经疾病“瘦素缺乏症”的发育途径紊乱。
Dev Biol. 1969 Aug;20(2):158-81. doi: 10.1016/0012-1606(69)90011-6.

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Purkinje Cell Signaling Deficits in Animal Models of Ataxia.共济失调动物模型中的浦肯野细胞信号缺陷
Front Synaptic Neurosci. 2018 Apr 26;10:6. doi: 10.3389/fnsyn.2018.00006. eCollection 2018.
2
Dystonia and cerebellar degeneration in the leaner mouse mutant.瘦型小鼠突变体中的肌张力障碍和小脑变性。
Brain Res. 2015 Jun 22;1611:56-64. doi: 10.1016/j.brainres.2015.03.011. Epub 2015 Mar 16.
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Animal models in epilepsy research: legacies and new directions.癫痫研究中的动物模型:遗产与新方向。
Nat Neurosci. 2015 Mar;18(3):339-43. doi: 10.1038/nn.3934. Epub 2015 Feb 24.
4
The spatial learning phenotype of heterozygous leaner mice is robust to systematic variation of the housing environment.杂合子“较瘦”小鼠的空间学习表型对饲养环境的系统性变化具有较强的耐受性。
Comp Med. 2009 Apr;59(2):129-38.
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Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a.Rocker是电压依赖性钙通道基因Cacna1a的一种新变体。
J Neurosci. 2001 Feb 15;21(4):1169-78. doi: 10.1523/JNEUROSCI.21-04-01169.2001.
6
Genetic analysis of voltage-dependent calcium channels.电压依赖性钙通道的遗传分析
J Bioenerg Biomembr. 1998 Aug;30(4):387-98. doi: 10.1023/a:1021993723565.
7
Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice.Cacnl1a4钙通道基因的突变与蹒跚和更瘦突变小鼠的癫痫发作、小脑变性和共济失调有关。
Mamm Genome. 1997 Feb;8(2):113-20. doi: 10.1007/s003359900369.