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A Signaling Mechanism Coupling Netrin-1/Deleted in Colorectal Cancer Chemoattraction to SNARE-Mediated Exocytosis in Axonal Growth Cones
Tiziana Cotrufo et al.
JOURNAL OF NEUROSCIENCE (2011)
Synaptophysin Is Required for Synaptobrevin Retrieval during Synaptic Vesicle Endocytosis
Sarah L. Gordon et al.
JOURNAL OF NEUROSCIENCE (2011)
The role of Synaptobrevin1/VAMP1 in Ca2+-triggered neurotransmitter release at the mouse neuromuscular junction
Yun Liu et al.
JOURNAL OF PHYSIOLOGY-LONDON (2011)
SNAP-23 and syntaxin-3 are required for chemokine release by mature human mast cells
Simon P. C. Frank et al.
MOLECULAR IMMUNOLOGY (2011)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret et al.
NATURE (2011)
A Single Amino Acid Mutation in SNAP-25 Induces Anxiety-Related Behavior in Mouse
Masakazu Kataoka et al.
PLOS ONE (2011)
Lack of the endosomal SNAREs vti1a and vti1b led to significant impairments in neuronal development
Ajaya J. Kunwar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Replication study of Japanese cohorts supports the role of STX1A in autism susceptibility
Kazuhiko Nakamura et al.
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY (2011)
Syntaxin7 Is Required for Lytic Granule Release from Cytotoxic T Lymphocytes
Varsha Pattu et al.
TRAFFIC (2011)
Syntaxin 11 Binds Vti1b and Regulates Late Endosome to Lysosome Fusion in Macrophages
Carolin Offenhaeuser et al.
TRAFFIC (2011)
The Role of VAMP7/TI-VAMP in Cell Polarity and Lysosomal Exocytosis in vivo
Mahito Sato et al.
TRAFFIC (2011)
Association Study of SNAP25 and Schizophrenia in Irish Family and Case-Control Samples
A. H. Fanous et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2010)
Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2
Marie Meeths et al.
BLOOD (2010)
The Longin SNARE VAMP7/TI-VAMP Adopts a Closed Conformation
Sandro Vivona et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Rapid neurite outgrowth in neurosecretory cells and neurons is sustained by the exocytosis of a cytoplasmic organelle, the enlargeosome
Gabriella Racchetti et al.
JOURNAL OF CELL SCIENCE (2010)
Syntaxin 16: Unraveling Cellular Physiology Through a Ubiquitous SNARE Molecule
Yanan Chen et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2010)
STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5
Valentina Cetica et al.
JOURNAL OF MEDICAL GENETICS (2010)
Munc18-1 as a key regulator of neurosecretion
Gayoung A. Han et al.
JOURNAL OF NEUROCHEMISTRY (2010)
A SNAP25 promoter variant is associated with early-onset bipolar disorder and a high expression level in brain
B. Etain et al.
MOLECULAR PSYCHIATRY (2010)
Loss of SNAP29 Impairs Endocytic Recycling and Cell Motility
Debora Rapaport et al.
PLOS ONE (2010)
Intelligence in Williams Syndrome Is Related to STX1A, Which Encodes a Component of the Presynaptic SNARE Complex
Michael C. Gao et al.
PLOS ONE (2010)
Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules
Genevieve de Saint Basile et al.
NATURE REVIEWS IMMUNOLOGY (2010)
Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11
Udo zur Stadt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
GOSR2 Lys67Arg Is Associated With Hypertension in Whites
Tamra E. Meyer et al.
AMERICAN JOURNAL OF HYPERTENSION (2009)
Evidence That Putative ADHD Low Risk Alleles at SNAP25 May Increase the Risk of Schizophrenia
L. S. Carroll et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
De Novo STXBP1 Mutations in Mental Retardation and Nonsyndromic Epilepsy
Fadi F. Hamdan et al.
ANNALS OF NEUROLOGY (2009)
A role for endobrevin/VAMP8 in CTL lytic granule exocytosis
Li Shen Loo et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2009)
Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk
Peter L. Oliver et al.
HUMAN MOLECULAR GENETICS (2009)
Expression and subcellular localization of syntaxin 11 in human neutrophils
Li-xin Xie et al.
INFLAMMATION RESEARCH (2009)
Munc18-1 binding to the neuronal SNARE complex controls synaptic vesicle priming
Ferenc Deak et al.
JOURNAL OF CELL BIOLOGY (2009)
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
Marjorie Cote et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Membrane Fusion: Grappling with SNARE and SM Proteins
Thomas C. Sudhof et al.
SCIENCE (2009)
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
Nicholas T. Gorden et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle
Jonna Tallila et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Syntaxin 1A is required for normal in utero development
John E. McRory et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)
Syntaxin-11 is expressed in primary human monocytes/macrophages and acts as a negative regulator of macrophage engulfment of apoptotic cells and IgG-opsonized target cells
Shouting Zhang et al.
BRITISH JOURNAL OF HAEMATOLOGY (2008)
Vesicle associated membrane protein (VAMP)-7 and VAMP-8, but not VAMP-2 or VAMP-3, are required for activation-induced degranulation of mature human mast cells
Leif E. Sander et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2008)
Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts
M. F. Gosso et al.
GENES BRAIN AND BEHAVIOR (2008)
Genetic and expression analyses reveal elevated expression of syntaxin 1A (STX1A) in high functioning autism
Kazuhiko Nakamura et al.
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY (2008)
The regulated exocytosis of enlargeosomes is mediated by a SNARE machinery that includes VAMP4
Emanuele Cocucci et al.
JOURNAL OF CELL SCIENCE (2008)
Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype
Marilee A. Martens et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2008)
Munc18a Scaffolds SNARE Assembly to Promote Membrane Fusion
Travis L. Rodkey et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy
Hirotomo Saitsu et al.
NATURE GENETICS (2008)
An Ancient Duplication of Exon 5 in the Snap25 Gene Is Required for Complex Neuronal Development/Function
Jenny U. Johansson et al.
PLOS GENETICS (2008)
Search for genetic variants of the SYNTAXIN 1A (STX1A) gene:: the -352 A>T variant in the STX1A promoter associates with impaired glucose metabolism in an Italian obese population
S. Romeo et al.
INTERNATIONAL JOURNAL OF OBESITY (2008)
Cutting edge: Syntaxin 11 regulates lymphocyte-mediated secretion and cytotoxicity
Laura N. Arneson et al.
JOURNAL OF IMMUNOLOGY (2007)
Lack of Gnas epigenetic changes and pseudohypoparathyroidism type Ib in mice with targeted disruption of syntaxin-16
Leopold F. Frohlich et al.
ENDOCRINOLOGY (2007)
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse
Alexander F. Jeans et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutant
Arne M. Nystuen et al.
NEUROGENETICS (2007)
The SNAP-25 gene is associated with cognitive ability:: evidence from a family-based study in two independent Dutch cohorts
M. F. Gosso et al.
MOLECULAR PSYCHIATRY (2006)
Analysis of knock-out mice to determine the role of HPC-1/syntaxin 1A in expressing synaptic plasticity
Tomonori Fujiwara et al.
JOURNAL OF NEUROSCIENCE (2006)
Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis:: association with disease-free remissions and haematopoietic malignancies -: art. no. e14
E Rudd et al.
JOURNAL OF MEDICAL GENETICS (2006)
SNAREs - engines for membrane fusion
Reinhard Jahn et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2006)
The v-SNARE Vti1a regulates insulin-stimulated glucose transport and Acrp30 secretion in 3T3-L1 adipocytes
A Bose et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma
E Sprecher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS
A Linglart et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
U zur Stadt et al.
HUMAN MOLECULAR GENETICS (2005)
Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB
J Liu et al.
HUMAN MOLECULAR GENETICS (2005)
Activation-induced polarized recycling targets T cell antigen receptors to the immunological synapse: Involvement of SNARE complexes
V Das et al.
IMMUNITY (2004)
Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD
J Mill et al.
MOLECULAR PSYCHIATRY (2004)
Longins and their longin domains: regulated SNAREs and multifunctional SNARE regulators
V Rossi et al.
TRENDS IN BIOCHEMICAL SCIENCES (2004)
Ultrastructural characterization of endoplasmic reticulum - Golgi transport containers (EGTC)
H Horstmann et al.
JOURNAL OF CELL SCIENCE (2002)
Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients
YQ Wu et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder
J Mill et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform
F Mallard et al.
JOURNAL OF CELL BIOLOGY (2002)
Genetic ablation of the t-SNARE SNAP-25 distinguishes mechanisms of neuroexocytosis
P Washbourne et al.
NATURE NEUROSCIENCE (2002)
SNARE function analyzed in synaptobrevin/VAMP knockout mice
S Schoch et al.
SCIENCE (2001)
Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients
K Tsunoda et al.
DIABETOLOGIA (2001)
Munc18-1 promotes large dense-core vesicle docking
T Voets et al.
NEURON (2001)
SNAP-29 is a promiscuous syntaxin-binding SNARE
AC Hohenstein et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
A novel SNARE N-terminal domain revealed by the crystal structure of Sec22b
LC Gonzalez et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Polymorphism in SNAP29 gene promoter region associated with schizophrenia
T Saito et al.
MOLECULAR PSYCHIATRY (2001)
Subunit structure of a mammalian ER/Golgi SNARE complex
DL Xu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Syntaxin 11 is an atypical SNARE abundant in the immune system
R Prekeris et al.
EUROPEAN JOURNAL OF CELL BIOLOGY (2000)
Testing the 3Q:1R rule:: Mutational analysis of the ionic zero layer in the yeast exocytic SNARE complex reveals no requirement for arginine
L Katz et al.
MOLECULAR BIOLOGY OF THE CELL (2000)
The R-SNARE endobrevin/VAMP-8 mediates homotypic fusion of early endosomes and late endosomes
W Antonin et al.
MOLECULAR BIOLOGY OF THE CELL (2000)
Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder
CL Barr et al.
MOLECULAR PSYCHIATRY (2000)
Munc18-2, a functional partner of syntaxin 3, controls apical membrane trafficking in epithelial cells
K Riento et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Synaptic assembly of the brain in the absence of neurotransmitter secretion
M Verhage et al.
SCIENCE (2000)
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