Add to ORKGGene identification in 1.6-Mb region of the Down syndrome region on chromosome 2
A repeat complex in the mitochondrial control region of Adelie penguins from Antarctic
New Cdc2 Tyr 4 phosphorylation by dsRNA-activated protein kinase triggers Cdc2 polyubiquitination an...
In silico reversal of repeat-induced point mutation (RIP) identifies the origins of repeat families...
Evidence for involvement of a tumor suppressor gene on 1p in malignant peripheral nerve sheath tumor
A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susce...
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificatio
Genes in two MHC class I regions control recognition of a single rat NK cell allodeterminan
Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotenc...
Identification and validation of reference genes for gene expression studies in water buffal
Distinct gene expression profiles in subsets of chronic lymphocytic leukemia expressing stereotyped ...
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell lin
Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees
Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient...
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorde
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutati...
A repeat complex in the mitochondrial control region of Adelie penguins from Antarctic
New Cdc2 Tyr 4 phosphorylation by dsRNA-activated protein kinase triggers Cdc2 polyubiquitination an...
In silico reversal of repeat-induced point mutation (RIP) identifies the origins of repeat families...
Evidence for involvement of a tumor suppressor gene on 1p in malignant peripheral nerve sheath tumor
A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susce...
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificatio
Genes in two MHC class I regions control recognition of a single rat NK cell allodeterminan
Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotenc...
Identification and validation of reference genes for gene expression studies in water buffal
Distinct gene expression profiles in subsets of chronic lymphocytic leukemia expressing stereotyped ...
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell lin
Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees
Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient...
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorde
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutati...
A repeat complex in the mitochondrial control region of Adelie penguins from Antarctic
New Cdc2 Tyr 4 phosphorylation by dsRNA-activated protein kinase triggers Cdc2 polyubiquitination an...
In silico reversal of repeat-induced point mutation (RIP) identifies the origins of repeat families...