| scholarly article | Q13442814 |
| P50 | author | Stephen W. Scherer | Q7610775 |
| P2093 | author name string | Peter N Ray | |
| John B Vincent | |||
| Felipe A Cisternas | |||
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| Role of synaptotagmin, a Ca2+ and inositol polyphosphate binding protein, in neurotransmitter release and neurite outgrowth | Q33652647 | ||
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| The road taken: past and future foundations of membrane traffic | Q33824729 | ||
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| CAPS (Mammalian UNC-31) Protein Localizes to Membranes Involved in Dense-Core Vesicle Exocytosis | Q39758529 | ||
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| Synaptotagmins: C2-domain proteins that regulate membrane traffic | Q41118335 | ||
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| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | protein family | Q417841 |
| Dystrophin, muscular dystrophy | Q14864296 | ||
| Ca2+-dependent activator protein for secretion 2 | Q21499016 | ||
| Ca2+-dependent secretion activator | Q21983618 | ||
| P304 | page(s) | 279-91 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family | |
| P478 | volume | 81 |
| Q28207770 | A family of Ca2+-dependent activator proteins for secretion: comparative analysis of structure, expression, localization, and function |
| Q28274390 | A heterogeneity-based genome search meta-analysis for autism-spectrum disorders |
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| Q33281834 | Alternative splicing variations in mouse CAPS2: differential expression and functional properties of splicing variants |
| Q35728813 | Analysis of striatal transcriptome in mice overexpressing human wild-type alpha-synuclein supports synaptic dysfunction and suggests mechanisms of neuroprotection for striatal neurons |
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| Q31165335 | Axonal localization of Ca2+-dependent activator protein for secretion 2 is critical for subcellular locality of brain-derived neurotrophic factor and neurotrophin-3 release affecting proper development of postnatal mouse cerebellum. |
| Q33892169 | Bio-collections in autism research |
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| Q28570841 | Ca2+-dependent activator proteins of secretion promote vesicular monoamine uptake |
| Q30497843 | Calcium-dependent activator protein for secretion 2 (CAPS2) promotes BDNF secretion and is critical for the development of GABAergic interneuron network |
| Q37399985 | Developmentally regulated Ca2+-dependent activator protein for secretion 2 (CAPS2) is involved in BDNF secretion and is associated with autism susceptibility. |
| Q46967226 | Differential distributions of the Ca2+ -dependent activator protein for secretion family proteins (CAPS2 and CAPS1) in the mouse brain |
| Q33895169 | Effects of IKAP/hELP1 Deficiency on Gene Expression in Differentiating Neuroblastoma Cells: Implications for Familial Dysautonomia |
| Q51685341 | Exploiting microRNA and mRNA profiles generated in vitro from carcinogen-exposed primary mouse hepatocytes for predicting in vivo genotoxicity and carcinogenicity |
| Q36745020 | Functional screen identifies regulators of murine hematopoietic stem cell repopulation |
| Q38843519 | Genetic Characterization of Dog Personality Traits. |
| Q50306738 | Genetics of autism |
| Q34677358 | Identification of Two Distinct Carcinoma-Associated Fibroblast Subtypes with Differential Tumor-Promoting Abilities in Oral Squamous Cell Carcinoma |
| Q58070547 | Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population |
| Q48250865 | Impaired cerebellar development and function in mice lacking CAPS2, a protein involved in neurotrophin release. |
| Q34372289 | Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients. |
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| Q37434709 | Mouse models of mutations and variations in autism spectrum disorder-associated genes: mice expressing Caps2/Cadps2 copy number and alternative splicing variants |
| Q36485097 | Reduced axonal localization of a Caps2 splice variant impairs axonal release of BDNF and causes autistic-like behavior in mice. |
| Q93139348 | SNPs associated with body weight and backfat thickness in two pig breeds identified by a genome-wide association study |
| Q84231464 | Submicroscopic deletion in 7q31 encompassing CADPS2 and TSPAN12 in a child with autism spectrum disorder and PHPV |
| Q48319540 | The genomic landscape of two Burkitt lymphoma cases and derived cell lines: comparison between primary and relapse samples. |
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| Q48340015 | Tissue distribution of Ca2+-dependent activator protein for secretion family members CAPS1 and CAPS2 in mice |
| Q47068719 | UNC-31 (CAPS) is required for dense-core vesicle but not synaptic vesicle exocytosis in Caenorhabditis elegans. |
| Q24616471 | Voxelwise genome-wide association study (vGWAS) |
| Q35064189 | Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis |
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