Mapping of Nakano cataract gene nct on mouse chromosome 16.
作者信息
Hiai H, Kato S, Horiuchi Y, Shimada R, Tsuruyama T, Watanabe T, Matsuzawa A
机构信息
Graduate School of Medicine, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto, 606.
出版信息
Genomics. 1998 May 15;50(1):119-20. doi: 10.1006/geno.1998.5286.
PMID:9628833
Abstract
摘要
相似文献
1
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.
2
Genetic analysis of Nakano Cataract and its modifier genes in mice.小鼠中野白内障及其修饰基因的遗传分析。
Exp Eye Res. 2002 Dec;75(6):745-51. doi: 10.1006/exer.2002.2068.
3
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.
4
A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.一个导致常染色体隐性白内障的基因定位于3号染色体短臂。
Isr Med Assoc J. 2001 Aug;3(8):559-62.
5
Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract.人类CP49基因的定位及一个基因内多态性标记的鉴定，以用于常染色体显性先天性白内障的遗传连锁分析。
Biochem Biophys Res Commun. 2000 Apr 13;270(2):432-6. doi: 10.1006/bbrc.2000.2442.
6
Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.小鼠αA-晶体蛋白编码基因中一种新的显性V124E突变的特征分析
Invest Ophthalmol Vis Sci. 2001 Nov;42(12):2909-15.
7
Retarded and distinct progress of lens opacification in congenic hereditary cataract mice, Balb/c-nct/nct.同源遗传性白内障小鼠Balb/c-nct/nct晶状体混浊进展迟缓且有明显差异。
Exp Eye Res. 1988 Nov;47(5):705-11. doi: 10.1016/0014-4835(88)90038-3.
8
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.
9
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.
10
A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.19号染色体上常染色体显性白内障的一个新基因座：连锁分析及候选基因筛查
Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3441-9. doi: 10.1167/iovs.05-1035.
Zotero 插件