Congenital cataracts: gene mapping

被引：39

作者：

He, WG

Li, SB

机构：

[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

[2] Univ S Alabama, Dept Med Genet, Mobile, AL 36688 USA

来源：

HUMAN GENETICS | 2000年 / 106卷 / 01期

关键词：

D O I：

10.1007/s004390051002

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Congenital cataracts are one of the major causes of induced blindness in children. Gene mapping is an important step in understanding the molecular defects of congenital cataracts. Some congenital cataract genes have been mapped, and more genes will be located and identified in the future. The locations and candidate locations of congenital cataract genes are discussed in this review.

引用

收藏

页码：1 / 13

页数：13

相关论文

共 210 条

[21] A chromosomal deletion map of human malformations [J].

Brewer, C ;

Holloway, S ;

Zawalnyski, P ;

Schinzel, A ;

FitzPatrick, D .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1153-1159

[22] GENETIC-LINKAGE OF WAGNER DISEASE AND EROSIVE VITREORETINOPATHY TO CHROMOSOME 5Q13-14 [J].

BROWN, DM ;

GRAEMIGER, RA ;

HERGERSBERG, M ;

SCHINZEL, A ;

MESSMER, EP ;

NIEMEYER, G ;

SCHNEEBERGER, SA ;

STREB, LM ;

TAYLOR, CM ;

KIMURA, AE ;

WEINGEIST, TA ;

SHEFFIELD, C ;

STONE, EM .

ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (05) :671-675

[23] Ocular retardation mouse caused by Chx10 homeobox null allele: Impaired retinal progenitor proliferation and bipolar cell differentiation [J].

Burmeister, M ;

Novak, T ;

Liang, MY ;

Basu, S ;

Ploder, L ;

Hawes, NL ;

Vidgen, D ;

Hoover, F ;

Goldman, D ;

Kalnins, VI ;

Roderick, TH ;

Taylor, BA ;

Hankin, MH ;

McInnes, RR .

NATURE GENETICS, 1996, 12 (04) :376-384

[24]

Camuzat A, 1996, HUM GENET, V97, P798

[25] OVEREXPRESSION OF THE VIMENTIN GENE IN TRANSGENIC MICE INHIBITS NORMAL LENS CELL-DIFFERENTIATION [J].

CAPETANAKI, Y ;

SMITH, S ;

HEATH, JP .

JOURNAL OF CELL BIOLOGY, 1989, 109 (04) :1653-1664

[26] IMMUNOCYTOCHEMICAL LOCALIZATION OF THE 27K BETA-CRYSTALLIN POLYPEPTIDE IN THE MOUSE LENS DURING DEVELOPMENT USING A SPECIFIC MONOCLONAL-ANTIBODY - IMPLICATIONS FOR CATARACT FORMATION IN THE PHILLY MOUSE [J].

CARPER, D ;

SMITHGILL, SJ ;

KINOSHITA, JH .

DEVELOPMENTAL BIOLOGY, 1986, 113 (01) :104-109

[27] IN-VITRO STUDIES ON THE ASSEMBLY PROPERTIES OF THE LENS PROTEINS CP49, CP115 - COASSEMBLY WITH ALPHA-CRYSTALLIN BUT NOT WITH VIMENTIN [J].

CARTER, JM ;

HUTCHESON, AM ;

QUINLAN, RA .

EXPERIMENTAL EYE RESEARCH, 1995, 60 (02) :181-192

[28] A FRAMESHIFT MUTATION IN THE GAMMA-E-CRYSTALLIN GENE OF THE ELO MOUSE [J].

CARTIER, M ;

BREITMAN, ML ;

TSUI, LC .

NATURE GENETICS, 1992, 2 (01) :42-45

[29] DOWN SYNDROME [J].

CATALANO, RA .

SURVEY OF OPHTHALMOLOGY, 1990, 34 (05) :385-398

[30]

CHAMBERS C, 1991, J BIOL CHEM, V266, P6742

← 1 2 3 4 5 6 7 8 9 10 →