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EIF4H encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. Additionally we are shipping EIF4H Antibodies (65) and EIF4H Proteins (11) and many more products for this protein.
Results demonstrate that eukaryotic translation initiation factor 4H (eIF4H) plays a crucial role in translational control.
Eukaryotic Initiation Factor (show EIF4G1 ELISA Kits) 4H Is under Transcriptional Control of p65/NF-kappaB (show NFkBP65 ELISA Kits).
Studies indicate that eIF4A (show EIF4A1 ELISA Kits) (DDX2), together with its accessory proteins eIF4B (show EIF4B ELISA Kits) and eIF4H, is thought to act as a helicase that unwinds secondary structures in the mRNA 5' UTR (show UTS2R ELISA Kits).
results suggest that eIF4H isoform 1 plays an important role in carcinogenesis through the activation of oncogenic signaling and could be a promising molecular target for cancer therapy
data indicate that eIF4B (show EIF4B ELISA Kits) and 4H stimulate the nuclease (show DCLRE1C ELISA Kits) activity of herpes simplex virus vhs, and they provide evidence that additional mammalian factors are required for targeting to the encephalomyocarditis virus IRES
eIF4H binding is required for herpes simplex virus virion host shutoff-induced degradation of many mRNAs, perhaps by targeting Vhs to mRNAs and to preferred sites within mRNAs.
The interaction of eIF4AI with two accessory factors, eIF4B (show EIF4B ELISA Kits) and eIF4H, was studied.
Study reports the topology of the eIF4A (show EIF4A1 ELISA Kits)/4G/4H helicase complex, which is built from multiple experimentally observed domain-domain contacts.
Data show that reduced levels of eIF4B (show EIF4B ELISA Kits), eIF4H, or polyA-binding protein, also trigger SG formation.
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
Williams-Beuren syndrome chromosome region 1
, eukaryotic translation initiation factor 4H
, Eukaryotic translation initiation factor 4H
, Williams-Beuren syndrome chromosome region 1 homolog
, williams-Beuren syndrome chromosomal region 1 protein homolog