Human ABCA3, a product of a responsible gene for abca3 for fatal surfactant deficiency in newborns, exhibits unique ATP hydrolysis activity and generates intracellular multilamellar vesicles-Reference-Cited by-同舟云学术

Human ABCA3, a product of a responsible gene for abca3 for fatal surfactant deficiency in newborns, exhibits unique ATP hydrolysis activity and generates intracellular multilamellar vesicles

Published:2004-11 Issue:1 Volume:324 Page:262-268
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Nagata Koh,Yamamoto Akitsugu,Ban Nobuhiro,Tanaka Arowu R.,Matsuo Michinori,Kioka Noriyuki,Inagaki Nobuya,Ueda Kazumitsu

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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4. The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3;Connors;Genomics,1997

5. Primary structure of a novel ABC transporter with a chromosomal localization on the band encoding the multidrug resistance-associated protein;Klugbauer;FEBS Lett.,1996

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