15q15

Recent genome-wide association studies (GWASs) have identified common genetic variants at 5p15.33, 6p21-6p22 and 15q25.1… (More)

Deletions and/or loss of heterozygosity (LOH) on chromosome 15 (15q15 and 15q21) have been found in several human tumors… (More)

D evelopmental dyslexia (dyslexia) is a heritable condition typically diagnosed in the first school years, characterised by an… (More)

Infection with immunosuppressive lentiviruses is associated with increased cancer risk,but most studies have implicated indirect… (More)

We isolated and characterized the gene encoding human transglutaminase (TG)(X) (TGM5) and mapped it to the 15q15.2 region of… (More)

The nature of subtypes in schizophrenia and the meaning of heterogeneity in schizophrenia have been considered a principal… (More)

Hydrogen peroxide is the final electron acceptor for the biosynthesis of thyroid hormone catalyzed by thyroperoxidase at the… (More)

Previous genetic and physical studies of LGMD2A, an autosomal recessive form of limb-girdle muscular dystrophy, have led to the… (More)

Oncogenic activation of the MCF.2 cell line-derived transforming sequence gene (MCF2) occurs through substitution of part of its… (More)

Protein 4.2 (P4.2), one of the major components of the red-blood-cell membrane, is located on the interior surface, where it… (More)