Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Andrew F X, Goldberg"'
Publikováno v:
Journal of molecular biology. 434(21)
Accurate quantitative estimates of protein-membrane interactions are critical to studies of membrane proteins. Here, we demonstrate that thermodynamic analyses based on current hydropathy scales do not account for the significant and experimentally d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4abf8fbad27f3afd26fb8225ef76f184
https://pubmed.ncbi.nlm.nih.gov/36115657
https://pubmed.ncbi.nlm.nih.gov/36115657
Autor:
Yagya V Sharma, Radu I Cojocaru, Linda M Ritter, Nidhi Khattree, Matthew Brooks, Alison Scott, Anand Swaroop, Andrew F X Goldberg
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e31371 (2012)
Inherited defects in retinal photoreceptor structure impair visual transduction, disrupt relationship with the retinal pigment epithelium (RPE), and compromise cell viability. A variety of progressive retinal degenerative diseases can result, and kno
Externí odkaz:
https://doaj.org/article/90ab2fc331f44d4fa2a526da284f3d96
Publikováno v:
The Journal of Membrane Biology. 124:199-206
Chloride channels were detergent-extracted fromTorpedo electroplax plasma membrane vesicles and reconstituted into liposomes by rapid detergent removal and a freeze-thawsonication procedure. Concentrative uptake of36Cl−, driven by a Cl− gradient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90963a7375958a7f2d4014abce5660e6
https://doi.org/10.1007/bf01994354
https://doi.org/10.1007/bf01994354
Autor:
Andrew F X, Goldberg
Publikováno v:
International review of cytology. 253
The vertebrate photoreceptor outer segment (OS) is a highly structured and dynamic organelle specialized to transduce light signals. The elaborate membranous architecture of the OS requires peripherin/rds (P/rds), an integral membrane protein and tet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::deb3148f90f34466940a7473a1a1dc04
https://pubmed.ncbi.nlm.nih.gov/17098056
https://pubmed.ncbi.nlm.nih.gov/17098056
Autor:
Linda M, Ritter, Kathleen, Boesze-Battaglia, Beatrice M, Tam, Orson L, Moritz, Nidhi, Khattree, Shu-Chu, Chen, Andrew F X, Goldberg
Publikováno v:
The Journal of biological chemistry. 279(38)
Inherited defects in the RDS gene cause a multiplicity of progressive retinal diseases in humans. The gene product, peripherin/rds (P/rds), is a member of the tetraspanin protein family required for normal vertebrate photoreceptor outer segment (OS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5744cb6b8f67898b4876f7ffe9f9a163
https://pubmed.ncbi.nlm.nih.gov/15252042
https://pubmed.ncbi.nlm.nih.gov/15252042