Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Wes D. Gifford"'
Autor:
Albert Lai, Jana Chtchetinin, Ethylin Wang Jabs, Sichen Li, Wes D. Gifford, William A. Paznekas
Publikováno v:
FEBS Journal. 276:6992-7005
Polarized membrane sorting of connexin 43 (Cx43) has not been well-characterized. Based on the presence of a putative sorting signal, YKLV(286-289), within its C-terminal cytoplasmic domain, we hypothesized that Cx43 is selectively expressed on the b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bda0424b547c202301005c98a313705
https://doi.org/10.1111/j.1742-4658.2009.07407.x
https://doi.org/10.1111/j.1742-4658.2009.07407.x
Autor:
Jana, Chtchetinin, Wes D, Gifford, Sichen, Li, William A, Paznekas, Ethylin Wang, Jabs, Albert, Lai
Publikováno v:
The FEBS journal. 276(23)
Polarized membrane sorting of Connexin 43 (Cx43) has not been well-characterized. Based on the presence of a putative sorting signal, Y286KLV289, within its carboxy terminal cytoplasmic domain, we hypothesized that Cx43 is selectively expressed on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa76369e24130c70c6548b0765a0c1e7
https://pubmed.ncbi.nlm.nih.gov/19860828
https://pubmed.ncbi.nlm.nih.gov/19860828
Autor:
Dung Nghi Le, Ethylin Wang Jabs, Andrew Charles, Wes D. Gifford, William A. Paznekas, Albert Lai
Publikováno v:
Journal of cell science. 119(Pt 3)
Oculodentodigital dysplasia (ODDD) is a rare developmental disorder characterized by craniofacial and limb abnormalities. Over 35 separate mutations in human connexin43 (Cx43) causing ODDD have been identified. Several mutations are also associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ce8f2b3a3b26deb37bf35356315fb2
https://pubmed.ncbi.nlm.nih.gov/16418219
https://pubmed.ncbi.nlm.nih.gov/16418219