Differential Clathrin Binding and Subcellular Localization of OCRL1 Splice Isoforms

Mutation of the inositol polyphosphate 5-phosphatase OCRL1 causes the X-linked disorder oculocerebrorenal syndrome of Lowe, characterized by defects in the brain, kidneys, and eyes. OCRL1 exists as two splice isoforms that differ by a single exon encoding 8 amino acids. The longer protein, termed is...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Choudhury, Rawshan, Noakes, Christopher J., McKenzie, Edward, Kox, Corinne, Lowe, Martin
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Biochemistry and Molecular Biology 2009
Gaiak:
Membrane Transport, Structure, Function, and Biogenesis
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2665120/
https://ncbi.nlm.nih.gov/pubmed/19211563
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807442200
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak