Location of DHX30 and GNB5 variants, dinucleotide variants culled from... | Download Scientific Diagram
Anti-DHX30 antibody (ab85687) | Abcam
Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
Nutlin-Induced Apoptosis Is Specified by a Translation Program Regulated by PCBP2 and DHX30 - ScienceDirect
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DHX30 Antibody (NBP1-26604): Novus Biologicals
Cureus | A Novel De Novo Mutation of the DHX30 Gene in a Patient With Neurodevelopmental Disorder, Severe Motor Impairment, and Absent Language (NEDMIAL) | Article
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DHX30 Gene - GeneCards | DHX30 Protein | DHX30 Antibody
DHX30 Champions | DHX30 Fund
Home | DHX30 Fund
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
The RNA helicase DHX30 coordinates cytoplasmic translation and mitochondrial function contributing to cancer cell survival | bioRxiv
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
DHX30 (NM_138615) Human Tagged ORF Clone – RC204467 | OriGene
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
DHX30 Polyclonal Antibody (PA5-57067)
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder - ScienceDirect
Devastating Diagnosis: Children with rare mutation meet for first time in Fort Lauderdale – WSVN 7News | Miami News, Weather, Sports | Fort Lauderdale
N-terminal 152 amino-acid residue-long domain of DHX30 (DHX30N), which... | Download Scientific Diagram
Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
DHX30 Antibodies & ELISA Kits, DHX30 Proteins
DHX30 antibody (28814-1-AP) | Proteintech
A Japanese adult and two girls with NEDMIAL caused by de novo missense variants in DHX30 | Human Genome Variation
