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heat shock protein that binds alpha-filamin [RGD, Feb 2006].. De plus, nous expédions HSPB7 Anticorps (64) et HSPB7 Protéines (12) et beaucoup plus de produits pour cette protéine.
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Mouse (Murine) HSPB7 Kit ELISA pour Sandwich ELISA - ABIN816314
Rüdebusch, Benkner, Poesch, Dörr, Völker, Grube, Hammer, Felix: Dynamic adaptation of myocardial proteome during heart failure development. dans PLoS ONE 2018
Loss of Hspb7 in zebrafish or human cardiomyocytes stimulated autophagic pathways and expression of the sister gene encoding Hspb5 (Montrer CRYAB Kits ELISA). Inhibiting autophagy caused FilaminC aggregation in HSPB7 mutant human cardiomyocytes and developmental cardiomyopathy in hspb7 mutant zebrafish embryos.
our findings characterize HSPB7 as an intercalated disc protein and suggest it has an essential role in maintaining intercalated disc integrity and conduction function in the adult heart.
Patients with central sleep apnea and congestive heart failure had higher T allele frequencies in the HSPB7 gene.
HSPB7 loci is associated in the pathophysiologuy of ischemic heart failure.
Results imply that HSBP7 is likely to be a tumor suppressor gene regulated by p53 (Montrer TP53 Kits ELISA) and its downregulation by hypermethylation may play a critical role in renal carcinogenesis.
HSPB7 is a potential early biomarker after MI and serves as an independent risk factor of ACS in patients with acute chest pain.
Overexpression of HSPB1 (Montrer HSPB1 Kits ELISA), as well as HSPB6 (Montrer HSPB6 Kits ELISA), HSPB7 and HSPB8 (Montrer HSPB8 Kits ELISA) independently protect against tachycardia remodeling by attenuation of the RhoA GTPase pathway at different levels.
Data show a significant association between a SNP in HSPB7 gene (rs1739843, minor allele frequency 39%) and idiopathic DCM.
The rs1738943 shows that although this SNP is located within HSPB7, it resides in a block of high LD that spans HSPB7 and a nearby gene, CLCNKA, which encodes a voltage-sensitive chloride channel (Montrer CLCA1 Kits ELISA) expressed mainly in the kidney.
Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease.
The authors found that deleting HSPB7 resulted in uncontrolled elongation of actin filaments and the formation of atypical actin filament bundles in cardiomyocytes.
these data indicate that MEF2 (Montrer MEF2C Kits ELISA) and AP-1 (Montrer JUN Kits ELISA) confer antagonistic regulation of Hspb7 gene expression in skeletal muscle, with implications for autophagy and muscle atrophy.
this paper shows that skeletal-muscle-specific ablation of the HspB7 causes postnatal death owing to a respiration defect, with progressive myopathy phenotypes in the diaphragm
HSPB7 is a potential early biomarker after MI and serves as an independent risk factor of ACS (Montrer Acsl1 Kits ELISA) in patients with acute chest pain.
These results imply that HspB2 (Montrer HSPB2 Kits ELISA) and HspB7 might be up-regulated by ethanol during the short-term differentiation of neural stem cells.
heat shock protein that binds alpha-filamin
cardiovascular heat shock protein
, heat shock 27kDa protein family, member 7 (cardiovascular)
, heat shock 27kD protein family, member 7 (cardiovascular)
, heat shock protein beta-7
, heat shock protein 25 kDa 2 (cardiovascular)
, protein p19/6.8
, heat shock 27kD protein family member 7