
DHX58 Gene - GeneCards | DHX58 Protein | DHX58 Antibody
2024年12月24日 · DHX58 (DExH-Box Helicase 58) is a Protein Coding gene. Diseases associated with DHX58 include Measles and Rabies. Among its related pathways are Innate …
LGP2 - Wikipedia
Probable ATP-dependent RNA helicase DHX58 also known as RIG-I-like receptor 3 (RLR-3) or RIG-I-like receptor LGP2 (RLR) is a RIG-I-like receptor dsRNA helicase enzyme that in …
DHX58 DExH-box helicase 58 [ (human)] - National Center for ...
2025年2月8日 · DHX58 expression positively correlate with osteogenic process. DHX58 overexpression enhances osteogenesis via the Wnt/beta-Catenin pathway. characterize the …
DExH-box 解旋酶 58(DHX58)基因 | MCE - MCE-生物活性分子 …
Enables double-stranded RNA binding activity; single-stranded RNA binding activity; and zinc ion binding activity. Involved in negative regulation of defense response and negative regulation of …
DHX58 DExH-box helicase 58 [ Homo sapiens (human) ]
2025年2月8日 · Enables several functions, including ATP hydrolysis activity; RNA binding activity; and zinc ion binding activity. Involved in negative regulation of type I interferon production and …
Host genetic susceptibility to viral infections: the role of type I ...
WNV-infected, Dhx58-deficient mice showed increased mortality but similar kinetics of IFNβ production and tissue viral loads compared with WT mice. In the brain they displayed …
Dhx58 DExH-box helicase 58 [ (house mouse)] - National Center …
2025年2月8日 · DHX58 expression positively correlate with osteogenic process. DHX58 overexpression enhances osteogenesis via the Wnt/beta-Catenin pathway. These findings …
Interferon-α stimulates DExH-box helicase 58 to prevent ... - PubMed
2024年4月15日 · This study provides mechanistic evidence that IFN-α stimulates DHX58 to promote the translation of m 6 A-modified Gpx4 mRNA, suggesting the potential clinical …
RNA 解旋酶 DDX5 通过调节 DHX58 和 NFκB 转录本上的 N6-甲基 …
RNA 解旋酶 DDX5 通过调节 DHX58 和 NFκB 转录本上的 N6-甲基腺苷水平来抑制抗病毒先天免疫,从而促进病毒感染。 PLoS Pathogens ( IF 5.5) Pub Date : 2021-04-28, DOI: …
DHX58人源基因|DHX58基因突变_致病性_靶点-RDDC官网
Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis. Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound …