Focus on molecules: X-linked Retinitis Pigmentosa 2 protein, RP2

被引：20

作者：

Evans, RJ ^{[1
]}

Hardcastle, AJ ^{[1
]}

Cheetham, ME ^{[1
]}

机构：

[1] UCL, Inst Ophthalmol, Div Mol & Cellular Neurosci, London EC1V 9EL, England

来源：

EXPERIMENTAL EYE RESEARCH | 2006年 / 82卷 / 04期

关键词：

RP2; X-Linked; retinal degeneration; tubulin; microtubules; chaperone; ADP ribosylation factor;

D O I：

10.1016/j.exer.2005.10.023

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

引用

页码：543 / 544

页数：2

共 4 条

[1] Functional overlap between retinitis pigmentosa 2 protein and the tubulin-specific chaperone cofactor C [J].

Bartolini, F ;

Bhamidipati, A ;

Thomas, S ;

Schwahn, U ;

Lewis, SA ;

Cowan, NJ .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (17) :14629-14634

[2] Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane [J].

Chapple, JP ;

Hardcastle, AJ ;

Grayson, C ;

Spackman, LA ;

Willison, KR ;

Cheetham, ME .

HUMAN MOLECULAR GENETICS, 2000, 9 (13) :1919-1926

[3] Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3 [J].

Grayson, C ;

Bartolini, F ;

Chapple, JP ;

Willison, KR ;

Bhamidipati, A ;

Lewis, SA ;

Luthert, PJ ;

Hardcastle, AJ ;

Cowan, NJ ;

Cheetham, ME .

HUMAN MOLECULAR GENETICS, 2002, 11 (24) :3065-3074

[4] Positional cloning of the gene for X-linked retinitis pigmentosa 2 [J].

Schwahn, U ;

Lenzner, S ;

Dong, J ;

Feil, S ;

Hinzmann, B ;

van Duijnhoven, G ;

Kirschner, R ;

Hemberger, M ;

Bergen, AAB ;

Rosenberg, T ;

Pinckers, AJLG ;

Fundele, R ;

Rosenthal, A ;

Cremers, FPM ;

Ropers, HH ;

Berger, W .

NATURE GENETICS, 1998, 19 (04) :327-332

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