Mapping of rupture of lens cataract (rlc) on mouse chromosome 14.
作者信息
Matsushima Y, Kamoto T, Iida F, Abujiang P, Honda Y, Hiai H
机构信息
Department of Laboratory Animal Science, Saitama Cancer Center Research Institute, Japan.
出版信息
Genomics. 1996 Sep 15;36(3):553-4. doi: 10.1006/geno.1996.0507.
PMID:8884285
Abstract
摘要
相似文献
1
Mapping of rupture of lens cataract (rlc) on mouse chromosome 14.
Genomics. 1996 Sep 15;36(3):553-4. doi: 10.1006/geno.1996.0507.
2
Rupture of lens cataract: a novel hereditary recessive cataract model in the mouse.
Exp Eye Res. 1997 Jan;64(1):107-13. doi: 10.1006/exer.1996.0192.
3
Mutation of Dock5, a member of the guanine exchange factor Dock180 superfamily, in the rupture of lens cataract mouse.鸟嘌呤交换因子Dock180超家族成员Dock5在晶状体破裂性白内障小鼠中的突变。
Exp Eye Res. 2008 May;86(5):828-34. doi: 10.1016/j.exer.2008.02.011. Epub 2008 Mar 2.
4
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16.
Invest Ophthalmol Vis Sci. 1997 Nov;38(12):2502-7.
5
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.Lop12，一种小鼠Crygd基因的突变，可导致类似于人类科波克白内障的晶状体混浊。
Genomics. 2000 Feb 1;63(3):314-20. doi: 10.1006/geno.1999.6054.
6
Mapping of Nakano cataract gene nct on mouse chromosome 16.中野白内障基因nct在小鼠16号染色体上的定位。
Genomics. 1998 May 15;50(1):119-20. doi: 10.1006/geno.1998.5286.
7
Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.与Cat4a相关的异常眼睛发育，Cat4a是8号染色体上的一种显性小鼠白内障突变。
Invest Ophthalmol Vis Sci. 1998 Sep;39(10):1863-9.
8
A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse.Crygc基因中的一个6碱基对缺失导致小鼠出现核性和放射性白内障。
Invest Ophthalmol Vis Sci. 2002 Jan;43(1):236-40.
9
Dense cataract and microphthalmia--new spontaneous mutation in BALB/c mice.致密性白内障和小眼畸形——BALB/c小鼠中的新自发突变
Comp Med. 2004 Jun;54(3):275-9.
10
Two interactive genes responsible for a new inherited cataract (RCT) in the mouse.两个相互作用的基因导致小鼠出现一种新的遗传性白内障（RCT）。
Mamm Genome. 2001 Apr;12(4):278-83. doi: 10.1007/s003350010281.
引用本文的文献
1
Upregulation of multiple signaling pathways by Dock5 deletion in epithelial cells.上皮细胞中Dock5缺失导致多种信号通路上调。
Mol Vis. 2017 Dec 31;23:1081-1092. eCollection 2017.
2
Mapping of new recessive cataract gene (lr2) in the mouse.小鼠中新的隐性白内障基因（lr2）的定位
Mamm Genome. 1997 Dec;8(12):927-31. doi: 10.1007/s003359900613.
3
A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.位于13号染色体上的显性“小带粉状”白内障新基因座。
Am J Hum Genet. 1997 Jun;60(6):1474-8. doi: 10.1086/515468.
Zotero 插件