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Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Additionally we are shipping Histone Deacetylase 7 Antibodies (171) and Histone Deacetylase 7 Proteins (13) and many more products for this protein.
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This study demonstrated a simple and straightforward method of quantifying proneural/mesenchymal markers in glioblastoma. Of note, HDAC7 expression might be a novel therapeutic target in glioblastoma treatment.
HDAC9 (show HDAC9 ELISA Kits) promotes tumor formation of glioblastoma via TAZ (show TAZ ELISA Kits)-mediated EGFR (show EGFR ELISA Kits) pathway activation.
Data suggest, in chronic hepatitis C virus infection, HDAC9 (histone deacetylase 9 (show HDAC9 ELISA Kits)) induction in liver regulates hepatic gluconeogenesis and systemic insulin (show INS ELISA Kits) resistance via deacetylation of FoxO1 (show FOXO1 ELISA Kits) (Forkhead box O 1) and HDAC3 (histone deacetylase 3 (show HDAC3 ELISA Kits)).
results indicate that HDAC9 variant rs2107595 may be not associated with IS risk in southern Han Chinese
Data show that miR (show MLXIP ELISA Kits)-376a and HDAC9 (show HDAC9 ELISA Kits) expression are inversely correlated in hepatocellular carcinoma and suggest that HDAC9 (show HDAC9 ELISA Kits)-mediated epigenetic modification may contribute to the down-regulation of the miR (show MLXIP ELISA Kits)-376 cluster in hepatocellular carcinoma.
identify a new target of ROCK signaling via myosin phosphatase subunit (MYPT1 (show PPP1R12A ELISA Kits)) and histone deacetylase (show HDAC1 ELISA Kits) (HDAC7) at the nuclear level
Gene expression studies in peripheral blood mononuclear cells revealed increased mRNA levels of HDAC9 (show HDAC9 ELISA Kits). Analysis of human atherosclerotic plaques revealed no association between rs2107595 and specific plaque characteristics.
Study identifies the miR (show MLXIP ELISA Kits)-34a-HDAC1 (show HDAC1 ELISA Kits)/HDAC7-HSP70 (show HSP70 ELISA Kits) K246 axis as a novel molecular signature predictive of therapy resistance.
The transcriptional function of HCS (show HLCS ELISA Kits) was shown by in vitro pull down and in vivo co-immunoprecipitation assays to depend on its interaction with the histone deacetylases HDAC1 (show HDAC1 ELISA Kits), HDAC2 (show HDAC2 ELISA Kits) and HDAC7
The hydroxamic acid pan-HDAC (show HDAC3 ELISA Kits) inhibitor TSA (show PRDX2 ELISA Kits) synergistically inhibit the viability.
This study demonstrated that hdac7 decrease in skeletal muscle in muscle atrophy.
HDAC7 in osteoclasts is an important molecular regulator of MITF (show MITF ELISA Kits) activity and bone homeostasis.
Hdac7 degradation enhances beta-catenin (show CTNNB1 ELISA Kits) transcriptional activity in growth plate chondrocytes.
In hepatic stellate cells, CYLD (show CYLD ELISA Kits) removed HDAC7 from the hepatocyte growth factor (show HGF ELISA Kits) promoter and induced HGF (show HGF ELISA Kits) expression.
Histone deacetylase 7 promotes Toll-like receptor 4 (show TLR4 ELISA Kits)-dependent proinflammatory gene expression in macrophages.
HDAC7 overexpression suppresses, whereas HDAC7 deletion enhances, osteoclastogenesis
Nuclear export of histone deacetylase 7 during thymic selection is required for immune self-tolerance
Splicing of histone deacetylase 7 modulates smooth muscle cell proliferation and neointima formation through nuclear beta-catenin (show CTNNB1 ELISA Kits) translocation.
Data suggest that HDAC7 nuclear export governs a self-sustaining autoexcitatory loop.
Data indicate that CTLs had high expression of the histone deacetylase (show HDAC1 ELISA Kits) HDAC7 but continually phosphorylated and exported this transcriptional repressor from the nucleus.
Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene has sequence homology to members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic domain. It represses MEF2 activity through recruitment of multicomponent corepressor complexes that include CtBP and HDACs. This encoded protein may play a role in hematopoiesis. Multiple alternatively spliced transcripts have been described for this gene but the full-length nature of some of them has not been determined.
histone deacetylase 7
, histone deacetylase 7A
, MEF-2 interacting transcription repressor (MITR) protein
, histone deacetylase 4/5-related protein
, histone deacetylase 7B