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Mutant p53 protein (zeige TP53 Proteine) (Mutp53) binds and sequesters RNA helicases p72/82 from microprocessor causing an attenuation of microRNAs (miRNAs) maturation.
DDX17 contributes to acquired gefitinib resistance through exportin (zeige XPO1 Proteine)/importin-dependent cytoplasmic shuttling and activation of beta-catenin (zeige CTNNB1 Proteine) in non-small lung cancer cells.
The miRNA biogenesis factors, DDX17 and KHSRP (zeige KHSRP Proteine), regulate the protein level of Ago2 (zeige EIF2C2 Proteine) in human cells.
DDX17 is a Sox2 (zeige SOX2 Proteine)-binding protein in estrogen receptor (zeige ESR1 Proteine)-positive breast cancer; in reporter responsive (RR) cells but not reporter unresponsive (RU) cells, DDX17 enhances the tumorigenic and stem-like features of Sox2 (zeige SOX2 Proteine) by promoting its binding to its target genes
Overexpression of p72 decreased Beclin1 (zeige BECN1 Proteine) expression partially by increasing miR (zeige MLXIP Proteine)-34-5p and miR (zeige MLXIP Proteine)-5195-3p expression in glioma cells.
Systematic Determination of Human Cyclin Dependent Kinase (zeige CDK1 Proteine) (CDK)-9 (zeige CDK9 Proteine) Interactome Identifies Novel Functions in RNA Splicing Mediated by the DDX5 (zeige DDX5 Proteine) and DDX17 RNA Helicases
Downregulation of DDX5 (zeige DDX5 Proteine) and DDX17 protein expression during myogenesis and epithelial-to-mesenchymal transdifferentiation contributes to the switching of splicing programs during these processes.
Depletion of DDX17 but not the related helicase DDX5 (zeige DDX5 Proteine) increased Rift Valley fever virus replication in human cells.
DDX17 promotes the production of HIV-1 infectious particles by modulating HIV-1 RNA metabolism.
Data indicate that transcriptional coregulator ddx5 (zeige DDX5 Proteine)/ddx17 RNA helicases can simultaneously regulate the transcriptional activity and alternative splicing of NFAT5 (zeige NFAT5 Proteine) transcription factor.
Data show that p72/DDX17 specifically interacts with the miR (zeige MLXIP Proteine)-132 loop sequence and influences the relative ratio of the mature mice miR (zeige MLXIP Proteine)-212/132 miRNAs.
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and splicesosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an ATPase activated by a variety of RNA species, but not by dsDNA. This protein, and that encoded by DDX5 gene, are more closely related to each other than to any other member of the DEAD box family. This gene can encode multiple isoforms due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) start codon.
DEAD (Asp-Glu-Ala-Asp) box polypeptide 17
, DEAD box polypeptide 17
, DEAD box protein p72
, DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 17 (72kD)
, RNA-dependent helicase p72
, probable ATP-dependent RNA helicase DDX17
, DEAD (Asp-Glu-Ala-Asp) box polypeptide 46
, DEAD box protein 17