Related references
Note: Only part of the references are listed.Novel splice variants of the amyotrophic lateral sclerosis-associated gene VAPB expressed in human tissues
T. Nachreiner et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)
A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum
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FASEB JOURNAL (2010)
Structural Requirements for VAP-B Oligomerization and Their Implication in Amyotrophic Lateral Sclerosis-associated VAP-B(P56S) Neurotoxicity
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Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis
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JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Electrostatic Interaction between Oxysterol-binding Protein and VAMP-associated Protein A Revealed by NMR and Mutagenesis Studies
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JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
AAV-mediated expression of wild-type and ALS-linked mutant VAPB selectively triggers death of motoneurons through a Ca2+-dependent ER-associated pathway
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JOURNAL OF NEUROCHEMISTRY (2010)
ALS-linked P56S-VAPB, an aggregated loss-of-function mutant of VAPB, predisposes motor neurons to ER stress-related death by inducing aggregation of co-expressed wild-type VAPB
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JOURNAL OF NEUROCHEMISTRY (2009)
Comparative proteomic analyses of the nuclear envelope and pore complex suggests a wide range of heretofore unexpected functions
Dzmitry G. Batrakou et al.
JOURNAL OF PROTEOMICS (2009)
The Amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors
Hiroshi Tsuda et al.
CELL (2008)
Reduced translocation of nascent prion protein during ER stress contributes to neurodegeneration
Neena S. Rane et al.
DEVELOPMENTAL CELL (2008)
VAPB interacts with and modulates the activity of ATF6
Christos Gkogkas et al.
HUMAN MOLECULAR GENETICS (2008)
FFAT rescues VAPA-mediated inhibition of ER-to-Golgi transport and VAPB-mediated ER aggregation
Derek C. Prosser et al.
JOURNAL OF CELL SCIENCE (2008)
Coordinated lipid transfer between the endoplasmic reticulum and the Golgi complex requires the VAP proteins and is essential for Golgi-mediated transport
Diego Peretti et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
A Drosophila Model of ALS: Human ALS-Associated Mutation in VAP33A Suggests a Dominant Negative Mechanism
Anuradha Ratnaparkhi et al.
PLOS ONE (2008)
hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction
Andrea Chai et al.
HUMAN MOLECULAR GENETICS (2008)
Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates
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JOURNAL OF NEUROSCIENCE (2007)
Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8)
Kohsuke Kanekura et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Efficient trafficking of ceramide from the endoplasmic reticulum to the Golgi apparatus requires a VAMP-associated protein-interacting FFAT motif of CERT
Miyuki Kawano et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Eph and NMDA receptors control Ca2+/calmodulin-dependent protein kinase II activation during C-elegans oocyte meiotic maturation
C Corrigan et al.
DEVELOPMENT (2005)
The pathobiology of amyotrophic lateral sclerosis: A proteinopathy?
MJ Strong et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2005)
Structural basis of FFAT motif-mediated ER targeting
SE Kaiser et al.
STRUCTURE (2005)
A highly conserved binding site in vesicle-associated membrane protein-associated protein (VAP) for the FFAT motif of lipid-binding proteins
CJR Loewen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Differential regulation of endoplasmic reticulum structure through VAP-Nir protein interaction
R Amarilio et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Gene recruitment of the activated INO1 locus to the nuclear membrane
JH Brickner et al.
PLOS BIOLOGY (2004)
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
AL Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Formation of stacked ER cisternae by low affinity protein interactions
EL Snapp et al.
JOURNAL OF CELL BIOLOGY (2003)
Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor
G Michaux et al.
BLOOD (2003)
Role of the yeast VAP homolog, Scs2p, in INO1 expression and phospholipid metabolism
S Kagiwada et al.
JOURNAL OF BIOCHEMISTRY (2003)
Vesicle-associated membrane protein-associated protein-A (VAP-A) interacts with the oxysterol-binding protein to modify export from the endoplasmic reticulum
JP Wyles et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Drosophila VAP-33A directs bouton formation at neuromuscular junctions in a dosage-dependent manner
G Pennetta et al.
NEURON (2002)
VAP-A binds promiscuously to both v- and tSNAREs
ML Weir et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
A sperm cytoskeletal protein that signals oocyte meiotic maturation and ovulation
MA Miller et al.
SCIENCE (2001)
Mouse VAP33 is associated with the endoplasmic reticulum and microtubules
PA Skehel et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)