相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Myoferlin is critical for endocytosis in endothelial cells
Pascal N. Bernatchez et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2009)
Caveolae as organizers of pharmacologically relevant signal transduction molecules
Hemal H. Patel et al.
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY (2008)
Cardiac-Specific Overexpression of Caveolin-3 Induces Endogenous Cardiac Protection by Mimicking Ischemic Preconditioning
Yasuo M. Tsutsumi et al.
CIRCULATION (2008)
Repair of injured plasma membrane by rapid Ca2+-dependent endocytosis
Vincent Idone et al.
JOURNAL OF CELL BIOLOGY (2008)
Caveolinopathy - New mutations and additional symptoms
Ahmed Aboumousa et al.
NEUROMUSCULAR DISORDERS (2008)
Caveolin regulates endocytosis of the muscle repair protein, dysferlin
Delia J. Hernandez-Deviez et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Ca2+ and synaptotagmin VII-dependent delivery of lysosomal membrane to nascent phagosomes
Cecilia Czibener et al.
JOURNAL OF CELL BIOLOGY (2006)
Normal myoblast fusion requires myoferlin
KR Doherty et al.
DEVELOPMENT (2005)
Impaired membrane resealing and autoimmune myositis in synaptotagmin VII-deficient mice
S Chakrabarti et al.
JOURNAL OF CELL BIOLOGY (2003)
Membrane proximal lysosomes are the major vesicles responsible for calcium-dependent exocytosis in nonsecretory cells
JK Jaiswal et al.
JOURNAL OF CELL BIOLOGY (2002)
Caveolin-3 knock-out mice develop a progressive cardiomyopathy and show hyperactivation of the p42/44 MAPK cascade
SE Woodman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains
DB Davis et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Dynamin family of mechanoenzymes
D Danino et al.
CURRENT OPINION IN CELL BIOLOGY (2001)
Plasma membrane repair is mediated by Ca2+-regulated exocytosis of lysosomes
A Reddy et al.
CELL (2001)
Caveolin-3 deficiency causes muscle degeneration in mice
Y Hagiwara et al.
HUMAN MOLECULAR GENETICS (2000)
Myoferlin, a candidate gene and potential modifier of muscular dystrophy
DB Davis et al.
HUMAN MOLECULAR GENETICS (2000)