Targeting gene expression to cones with human cone opsin promoters in recombinant AAV-Reference-Cited by-同舟云学术

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Targeting gene expression to cones with human cone opsin promoters in recombinant AAV

Published:2008-03-13 Issue:14 Volume:15 Page:1049-1055
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Komáromy A M,Alexander J J,Cooper A E,Chiodo V A,Acland G M,Hauswirth W W,Aguirre G D

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/gt200832.pdf

Reference38 articles.

1. Kohl S, Marx T, Giddings I, Jägle H, Jacobson SG, Apfelstedt-Sylla E et al. Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel. Nat Genet 1998; 19: 257–259.

2. Kohl S, Baumann B, Rosenberg T, Kellner U, Lorenz B, Vadalà M et al. Mutations in the cone photoreceptor G-protein α -subunit gene GNAT2 in patients with achromatopsia. Am J Hum Genet 2002; 71: 422–425.

3. Sundin OH, Yang JM, Li Y, Zhu D, Hurd JN, Mitchell TN et al. Genetic basis of total colourblindness among the Pingelapese islanders. Nat Genet 2000; 25: 289–293.

4. Sidjanin DJ, Lowe JK, McElwee JL, Milne BS, Phippen TM, Sargan DR et al. Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. Hum Mol Genet 2002; 11: 1823–1833.

5. Demirci FY, Gupta N, Radak AL, Rigatti BW, Mah TS, Milam AH et al. Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15. Am J Ophthalmol 2005; 139: 386–388.

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