Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
BIN1 encodes several isoforms of a nucleocytoplasmic adaptor protein, one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor. De plus, nous expédions BIN1 Anticorps (116) et BIN1 Kits (14) et beaucoup plus de produits pour cette protéine.
Showing 9 out of 14 products:
Meta-analysis validated the association of late onset Alzheimer disease with BIN1 (rs744373) variants.
The findings reveal the ability of Bin1 to modify actin dynamics and provide a possible mechanistic connection between Bin1 and tau-induced pathobiological changes of the actin cytoskeleton.
the association between the rs744373 polymorphism of BIN1 protein and late-onset Alzheimer's disease in East Asian, American, and European populations (Meta-Analysis)
Italian family with centronuclear myopathy, carrying a novel pathogenic mutation of BIN1 gene in heterozygous state, consistent with autosomal dominant inheritance.
bridging integrator 1 Gene rs7561528 polymorphism contributes to Alzheimer's disease susceptibility in East Asian and Caucasian populations
Findings indicated that BIN1 restoration in NSCLC could reverse PD-L1 (Montrer CD274 Protéines)-mediated immune escape by inactivating the c-MYC (Montrer MYC Protéines) and EGFR (Montrer EGFR Protéines)/mitogen-activated protein kinase (Montrer MAPK1 Protéines) pathways.
propose that efforts to define how genetic variants in BIN1 elevate the risk for Alzheimer's disease would behoove to consider BIN1 function in the context of its main expression in mature oligodendrocytes
The results emphasize an additional level of complexity in the regulation of the interaction between BIN1 and Tau dependent on the BIN1 isoforms.
Data (including data from studies using transgenic mice) suggest that the process leading to microparticle release from cardiac myocytes involves recruitment of CHMP4B (Montrer CHMP4A Protéines) protein to the forming microparticle membrane which also contains cBIN1; plasma cBIN1 is reduced in patients with heart failure as compared to control subjects. (CHMP4B (Montrer CHMP4A Protéines) = charged multivesicular body protein 4B (Montrer CHMP4B Protéines); cBIN1 = cardiac bridging integrator 1)
Low Bin1 expression is associated with esophageal squamous cell carcinoma.
Data (including data from studies using transgenic mice) suggest that the process leading to microparticle release from cardiac myocytes involves recruitment of CHMP4B (Montrer CHMP4B Protéines) protein to the forming microparticle membrane which also contains cBIN1; plasma cBIN1 is reduced in patients with heart failure as compared to control subjects. (CHMP4B (Montrer CHMP4B Protéines) = charged multivesicular body protein 4B (Montrer CHMP4B Protéines); cBIN1 = cardiac bridging integrator 1)
Bin1 and CD2AP (Montrer Cd2ap Protéines) keep APP (Montrer APP Protéines) and BACE1 (Montrer BACE Protéines) apart in early endosomes by distinct mechanisms in axon and dendrites. Individuals carrying variants of either factor would slowly accumulate Abeta (Montrer APP Protéines) in neurons increasing the risk for late-onset AD.
the depletion of BIN1 increases cellular BACE1 (Montrer BACE Protéines) levels through impaired endosomal trafficking and reduces BACE1 (Montrer BACE Protéines) lysosomal degradation, resulting in increased Ab production. Our findings provide a mechanistic role of BIN1 in the pathogenesis of Alzheimer disease (AD), as a novel genetic regulator of BACE1 (Montrer BACE Protéines) levels and Ab production
Data demonstrate that EHBP1L1 links Rab8 (Montrer RAB8A Protéines) and the Bin1-dynamin (Montrer DNM1 Protéines) complex, which generates membrane curvature and excises the vesicle at the endocytic recycling compartment for apical transport.
Findings show how cardiac deficiency in Bin1 function causes age- and stress-associated heart failure suggesting that Bin1 is a positive modifier of cardiac contractility that helps sustain adult heart function under stress conditions.
Reorganization of BIN1-induced microdomains recruits phosphorylated ryanodine receptors into dyads, increasing calcium signaling.
Bin1 mAb reduced colitis morbidity in mice while unprotected mice were characterized by severe lesions throughout the mucosa, rupture of lymphoid follicle, high-level neutrophil and lymphocyte infiltration into the mucosal areas, loss of surface crypts.
The release of BIN1 from hypo-poly(ADP-ribosyl)ated E2F1 (Montrer E2F1 Protéines) is a mechanism by which serum starvation promotes E2F1 (Montrer E2F1 Protéines)-induced apoptosis.
BIN1 interacts with MTM1 (Montrer MTM1 Protéines) in skeletal muscle.
Cardiac BIN1 folds T-tubule membrane, controlling ion flux and limiting arrhythmia.
Report remodeling of the t-t nano-architecture in the post-MI heart that extends to the remote region and dysregulation of junctophilin-2 (Montrer JPH2 Protéines) and bridging integrator 1.
This gene encodes several isoforms of a nucleocytoplasmic adaptor protein, one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor. Isoforms that are expressed in the central nervous system may be involved in synaptic vesicle endocytosis and may interact with dynamin, synaptojanin, endophilin, and clathrin. Isoforms that are expressed in muscle and ubiquitously expressed isoforms localize to the cytoplasm and nucleus and activate a caspase-independent apoptotic process. Studies in mouse suggest that this gene plays an important role in cardiac muscle development. Alternate splicing of the gene results in ten transcript variants encoding different isoforms. Aberrant splice variants expressed in tumor cell lines have also been described.
bridging integrator 1
, myc box-dependent-interacting protein 1-like
, amphiphysin II
, amphiphysin-like protein
, box dependant MYC interacting protein 1
, box-dependent myc-interacting protein 1
, myc box-dependent-interacting protein 1
, SH3 domain-containing protein 9
, amphiphysin 2
, myc box dependent interacting protein 1
, amphiphysin IIamph2