Luminal Heterodimeric Amino Acid Transporter Defective in Cystinuria

Mutations of the glycoprotein rBAT cause cystinuria type I, an autosomal recessive failure of dibasic amino acid transport (b(0,+) type) across luminal membranes of intestine and kidney cells. Here we identify the permease-like protein b(0,+)AT as the catalytic subunit that associates by a disulfide...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Pfeiffer, Rahel, Loffing, Jan, Rossier, Grégoire, Bauch, Christian, Meier, Christian, Eggermann, Thomas, Loffing-Cueni, Dominique, Kühn, Lukas C., Verrey, François
Format: Artigo
Sprog:Inglês
Udgivet: The American Society for Cell Biology 1999
Fag:
Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC25748/
https://ncbi.nlm.nih.gov/pubmed/10588648
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker