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Localization of the twitcher (twi) mutation on mouse chromosome 12.

作者信息

D'Eustachio P, Clarke V

机构信息

Department of Biochemistry, New York University Medical Center, New York 10016.

出版信息

Mamm Genome. 1993 Nov;4(11):684-6. doi: 10.1007/BF00360908.

DOI:10.1007/BF00360908
PMID:8281019
Abstract
摘要

相似文献

1
Localization of the twitcher (twi) mutation on mouse chromosome 12.小鼠12号染色体上抽搐(twi)突变的定位。
Mamm Genome. 1993 Nov;4(11):684-6. doi: 10.1007/BF00360908.
2
Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity.一种影响疾病严重程度的小鼠隐性多囊肾病突变及修饰位点的定位
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3
Paradoxical influence of acid beta-galactosidase gene dosage on phenotype of the twitcher mouse (genetic galactosylceramidase deficiency).酸性β-半乳糖苷酶基因剂量对震颤小鼠(遗传性半乳糖基神经酰胺酶缺乏症)表型的矛盾影响。
Hum Mol Genet. 2000 Jul 1;9(11):1699-707. doi: 10.1093/hmg/9.11.1699.
4
Genetic analysis of the tw73 haplotype of the mouse using deletion mutations: evidence for a parasitic lethal mutation.
Genet Res. 1982 Apr;39(2):111-20. doi: 10.1017/s0016672300020814.
5
The mouse polycystic kidney disease mutation (cpk) is located on proximal chromosome 12.小鼠多囊肾病突变(cpk)位于近端12号染色体上。
Genomics. 1991 Apr;9(4):778-81. doi: 10.1016/0888-7543(91)90376-p.
6
Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4.种内回交卷尾小鼠的单倍型分析证实了ct基因定位于4号染色体。
Mamm Genome. 1995 Apr;6(4):269-72. doi: 10.1007/BF00352414.
7
Mapping of the 75-kDa inositol polyphosphate-5-phosphatase (Inpp5b) to distal mouse chromosome 4 and its exclusion as a candidate gene for dysgenetic lens.75 kDa 肌醇多磷酸-5-磷酸酶(Inpp5b)在小鼠4号染色体远端的定位及其作为晶状体发育异常候选基因的排除。
Genomics. 1995 Jul 20;28(2):280-5. doi: 10.1006/geno.1995.1142.
8
Molecular mapping of the mouse ob mutation.小鼠ob基因突变的分子定位
Genomics. 1991 Dec;11(4):1054-62. doi: 10.1016/0888-7543(91)90032-a.
9
Tss (Tail-short Shionogi), a new short tail mutation found in the BALB/cMs strain, maps quite closely to the Tail-short (Ts) locus on mouse chromosome 11.
Exp Anim. 2000 Apr;49(2):131-5. doi: 10.1538/expanim.49.131.
10
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.丑角鱼鳞病(ichq):一种伴有鱼鳞病样皮炎的幼年致死性小鼠突变。
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本文引用的文献

1
The Twitcher mouse: an enzymatically authentic model of human globoid cell leukodystrophy (Krabbe disease).抽搐小鼠:人类球状细胞脑白质营养不良(克拉伯病)的酶学真实模型。
Brain Res. 1980 Dec 8;202(2):479-83. doi: 10.1016/0006-8993(80)90159-6.
2
Hereditary leucodystrophy in the mouse: the new mutant twitcher.小鼠遗传性脑白质营养不良:新突变体“抽搐小鼠”
Brain. 1980 Sep;103(3):695-710. doi: 10.1093/brain/103.3.695.
3
Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.三种血影蛋白基因的染色体定位:与小鼠和人类遗传性溶血性贫血的关系。
Proc Natl Acad Sci U S A. 1988 Nov;85(21):8121-5. doi: 10.1073/pnas.85.21.8121.
4
A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination.小鼠第12号染色体的连锁图谱:免疫球蛋白重链基因(Igh)的定位以及性别和干涉对重组的影响
Genetics. 1988 Dec;120(4):1073-83. doi: 10.1093/genetics/120.4.1073.
5
Krabbe disease locus mapped to chromosome 14 by genetic linkage.通过基因连锁分析,克拉伯病基因座被定位到14号染色体。
Am J Hum Genet. 1990 Jul;47(1):37-44.
6
A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group.人类基因组的综合遗传连锁图谱。美国国立卫生研究院/CEPH合作制图小组。
Science. 1992 Oct 2;258(5079):67-86.
7
A detailed linkage map of subtelomeric murine chromosome 12 region including the situs inversus mutation locus IV.
Mamm Genome. 1992;3(11):637-43. doi: 10.1007/BF00352481.
8
A genetic map of the mouse suitable for typing intraspecific crosses.一张适用于种内杂交分型的小鼠遗传图谱。
Genetics. 1992 Jun;131(2):423-47. doi: 10.1093/genetics/131.2.423.