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SYN3 is a member of the synapsin gene family. De plus, nous expédions Synapsin III Protéines (5) et Synapsin III Kits (1) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 34 products:
Rat (Rattus) Polyclonal SYN3 Primary Antibody pour ICC, IHC - ABIN1742209
Piccini, Perlini, Cancedda, Benfenati, Giovedì: Phosphorylation by PKA and Cdk5 Mediates the Early Effects of Synapsin III in Neuronal Morphological Maturation. dans The Journal of neuroscience : the official journal of the Society for Neuroscience 2015
This study demonstrated that synapsin 3 regulating GABA Release from Hippocampal Interneurons.
These findings support a reciprocal modulatory interaction of alpha-syn and synapsin III in the regulation of dopamine neuron synaptic function.
The results of this study show SynIII plays a central role in early stages of neuronal development involving phosphorylation-dependent neuronal survival, polarization, and neuritic growth
This study demonostrated that Epileptic synapsin triple knockout mice exhibit progressive long-term aberrant plasticity in the entorhinal cortex.
Behavioral and neurophysiological features of Syn3 knockout mice are characterized by observation of the development and progress of seizures from postnatal day 20 to 180.
Analysis of cultured neurons from wild-type and Syn I,II,III-deficient triple knock-out (TKO) mice shows that synaptic vesicles are severely dispersed in the absence of Syns.
Mice lacking synapsin III show abnormalities in explicit memory and conditioned fear
The functions of synapsins were examined by characterizing the phenotype of mice in which all three synapsin genes were knocked out.
Collectively, our results demonstrate a novel role for synapsin III in regulating the proliferation of neural progenitor cells in the adult hippocampal dentate gyrus.
These findings contribute to previous work showing dysregulation of Synapsins, particularly SYN2, in mood disorders and improve our understanding of the regulatory mechanisms that precipitate these changes likely leading to the BD or MDD phenotype.
Syn-3 may mimic Syn-1A in the ability to bind and modulate Cavs, but preferring Cav2.3 to perhaps participate in triggering fusion of newcomer insulin SGs during second-phase GSIS.
The variations of MnSOD (rs4880) and SYN III (rs3788470, rs3827336, rs5998557) were not major risk factors for PD among Chinese, at least in our study populations
A significant difference was determined between attention deficit hyperactivity disorder and synapsin III gene -631 C>G polymorphism compared to the control group.
A protein encoded by this locus was found to be differentially expressed in postmortem brains from patients with atypical frontotemporal lobar degeneration.
This protein has been found differentially expressed in thalami from patients with schizophrenia.
Evidence is not in favor of a large effect of synapsin III gene in the pathogenesis of schizophrenia.
A missense polymorphism, S470N, was identified in the synapsin III gene and appeared more frequently in individuals with schizophrenia. The site affected by the polymorphism, Ser470, was determined to be a substrate for mitogen-activated protein kinase.
Supports a role for synapsin III in a subset of African American patients with schizophrenia.
A trend towards significance was detected when the synapsin III -196A allele distribution was analyzed in Caucasian patients with schizophrenia and a cohort of subjects from the Czech Republic with bipolar disorder.
No evidence that the synapsin III locus as a major susceptibility locus contributing to attention deficit hyperactivity disorder.
the C/C genotype in rs133946 and the G/G genotype in rs133945 could be protecting factors against multiple sclerosis in the Basque population.
The variation in SYN III methylation studied is 1) not related to schizophrenia in the population sample or a monozygotic twin pair discordant for schizophrenia and 2) not related to the mRNA level of SYN IIIa in different human brain regions
Both the association studies and expression studies didn't support a major role for SYN3 in the susceptibility of schizophrenia in Irish and Chinese populations.
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms.
, synapsin 3a
, synapsin III isoform IIIa
, synapsin 3
, synapsin IIIa
, cN28H9.2 (synapsin III)