Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
Cureus | A Novel De Novo Mutation of the DHX30 Gene in a Patient With Neurodevelopmental Disorder, Severe Motor Impairment, and Absent Language (NEDMIAL) | Article
Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
Home | DHX30 Fund
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
Home | DHX30 Fund
DHX30 Champions | DHX30 Fund
The RNA helicase DHX30 coordinates cytoplasmic translation and mitochondrial function contributing to cancer cell survival | bioRxiv
Researchers determine how the p53 protein can lead cancer cells to their death
The DHX30 binding site on the NS1 protein is comprised of amino... | Download Scientific Diagram
Figure S6. Role of DHX30 in mitochondrial function, related to Figures... | Download Scientific Diagram
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
The RNA helicase DHX30 coordinates cytoplasmic translation and mitochondrial function contributing to cancer cell survival | bioRxiv
DHX30 Antibodies & ELISA Kits, DHX30 Proteins
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
DHX30 antibody (28814-1-AP) | Proteintech
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
DHX30 Polyclonal Antibody (A302-218A)
