Ocular albinism: evidence for a defect in an intracellular signal transduction system-Reference-Cited by-同舟云学术

Ocular albinism: evidence for a defect in an intracellular signal transduction system

Published:1999-09 Issue:1 Volume:23 Page:108-112
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Schiaffino M. Vittoria,d'Addio Marilena,Alloni Anna,Baschirotto Cinzia,Valetti Caterina,Cortese Katia,Puri Claudia,Bassi M. Teresa,Colla Cristina,De Luca Michele,Tacchetti Carlo,Ballabio Andrea

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0999_108.pdf

Reference21 articles.

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2. Nurnberg, B. & Ahnert-Hilger, G. Potential roles of heterotrimeric G proteins of the endomembrane system. FEBS Lett. 389 , 61–65 (1996).

3. Schiaffino, M.V. et al. The ocular albinism type 1 (OA1) gene product is a membrane glycoprotein localized to melanosomes. Proc. Natl Acad. Sci. USA 93, 9055–9060 ( 1996).

4. Horn, F. et al. GPCRDB: an information system for G protein-coupled receptors. Nucleic Acids Res. 26, 275– 279 (1998).

5. Altschul, S.F. et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25, 3389–3402 (1997).

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