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Results 1 - 10 of 31 > >>
EC Number
Disease
PubMed ID
Title of Publication
Category
Confidence Level
Heart Defects, Congenital
Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.
unassigned
0
Carcinoma, Hepatocellular
Clinical implications of arrest-defective protein 1 expression in hepatocellular carcinoma: a novel predictor of microvascular invasion.
unassigned
0
Atherosclerosis
miRNA-27b modulates endothelial cell angiogenesis by directly targeting Naa15 in atherogenesis.
unassigned
0
Adenocarcinoma
Combined Phenotype of 4 Markers Improves Prognostic Value of Patients With Colon Cancer.
unassigned
0
Neoplasms
Phosphorylation of ARD1 by IKKbeta contributes to its destabilization and degradation.
unassigned
0
Intellectual Disability
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability.
unassigned
0
Intellectual Disability
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.
unassigned
0
Heart Defects, Congenital
Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.
therapeutic application
1
Carcinoma, Hepatocellular
Clinical implications of arrest-defective protein 1 expression in hepatocellular carcinoma: a novel predictor of microvascular invasion.
causal interaction
1
Carcinogenesis
hNaa10p contributes to tumorigenesis by facilitating DNMT1-mediated tumor suppressor gene silencing.
causal interaction
1
Results 1 - 10 of 31 > >>