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Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Additionally we are shipping Histone Deacetylase 9 Antibodies (117) and Histone Deacetylase 9 Proteins (9) and many more products for this protein.
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HDAC9 promotes angiogenesis and transcriptionally represses the endothelial cell miR-17-92 cluster.
Polymorphisms of HDAC9 is associated with Ischemic Stroke.
The results imply that HDAC9 is involved in the transcriptional regulation of human odontoblasts in vivo.
HDAC9 was commonly expressed in retinoblastoma tissues and HDAC9 was overexpressed in prognostically poor retinoblastoma patients.
HDAC9 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) 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 expression are inversely correlated in hepatocellular carcinoma and suggest that HDAC9-mediated epigenetic modification may contribute to the down-regulation of the miR (show MLXIP ELISA Kits)-376 cluster in hepatocellular carcinoma.
Gene expression studies in p (show APOE ELISA Kits)eripheral blood mononuclea (show APOE ELISA Kits)r cells revealed increased mRNA levels of HDAC9. Analysis of human atherosclerotic plaques revealed no association between rs2107595 and specific plaque characteristics.
The hydroxamic acid pan-HDAC (show HDAC3 ELISA Kits) inhibitor TSA (show PRDX2 ELISA Kits) synergistically inhibit the viability.
The results elucidate the genetic etiology of lung adenocarcinoma by demonstrating that SNP rs10248565 in the HDAC9 gene may be a potential biomarker of cancer susceptibility.
Xenograft study in nude mice showed that downregulation of HDAC9 inhibited tumor growth and development in vivo.
Dach2 (show DACH2 ELISA Kits) and Hdac9 mediate the effects of muscle activity on muscle reinnervation; Myog (show MYOG ELISA Kits) and Gdf5 (show GDF5 ELISA Kits) appear to stimulate muscle reinnervation through parallel pathways
HDAC9 is a novel, important and physiologically relevant modulator of bone remodeling and skeletal homeostasis.
Class IIa HDAC9 interact with Class IIb HDAC6 to modulate cell movement and survival in GnRH neurons
Compared with HDAC9(+/+)ApoE (show APOE ELISA Kits)(-/-) mice, HDAC9(-/-)ApoE (show APOE ELISA Kits)(-/-) mice exhibited markedly reduced lesion sizes throughout atherosclerotic aortas and significantly less advanced lesions.
HDAC9 deletion decreased atherosclerosis in LDLr (show LDLR ELISA Kits)(-/-) mice with minimal effect on plasma lipids. Macrophage HDAC9 upregulation is atherogenic via suppression of cholesterol efflux and generation of alternatively activated macrophages in atherosclerosis.
Genetic ablation of HDAC9 improves adipogenic differentiation and systemic metabolic state during a high-fat diet, resulting in diminished weight gain, improved glucose tolerance and insulin (show INS ELISA Kits) sensitivity, and reduced hepatosteatosis.
Dephosphorylation at a conserved SP motif governs cAMP sensitivity and nuclear localization of class IIa histone deacetylases HDAC4 (show HDAC5 ELISA Kits), 5 and 9
HDAC9 is responsible for repressing ChAT gene expression in NG108-15 neuronal cells and thus plays an important role in cholinergic differentiation.
HDA9 prevents precocious flowering under SD conditions by curbing the hyperactivation of AGL19, an upstream activator of FT, through resetting the local chromatin environment.
HDA9 negatively influences germination and is involved in the suppression of seedling traits in dry seeds, probably by transcriptional repression via histone deacetylation.
The data indicate thatHDA9 represses flowering by repressing AGL19 gene expressionindependently of CONSTANS or FLC pathways.
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 9
, histone deacetylase 9-B
, MEF-2 interacting transcription repressor (MITR) protein
, histone deacetylase 4/5-related protein
, histone deacetylase 7B
, MEF2-interacting transcription repressor MITR
, histone deacetylase-related protein
, histone deacetylase 9, MITR protein