DHX30 Polyclonal Antibody (A302-218A)
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
Home | DHX30 Fund
Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders | Genome Medicine | Full Text
DHX30 Antibody (NBP1-26604): Novus Biologicals
Devastating Diagnosis: Children with rare mutation meet for first time in Fort Lauderdale – WSVN 7News | Miami News, Weather, Sports | Fort Lauderdale
DHX30 antibody (28814-1-AP) | Proteintech
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
DHX30 (NM_138615) Human Tagged ORF Clone – RC204467 | OriGene
A Japanese adult and two girls with NEDMIAL caused by de novo missense variants in DHX30 | Human Genome Variation
Cancers | Free Full-Text | DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates | Scientific Reports
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DHX30 Antibodies & ELISA Kits, DHX30 Proteins
Cureus | A Novel De Novo Mutation of the DHX30 Gene in a Patient With Neurodevelopmental Disorder, Severe Motor Impairment, and Absent Language (NEDMIAL) | Article
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
The DHX30 binding site on the NS1 protein is comprised of amino... | Download Scientific Diagram
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
Anti-DHX30 antibody (ab85687) | Abcam
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 - ScienceDirect
