Human neutrophils are highly specialised for their primary function, ie phagocytosis and
destruction of microorganisms. Leukocyte recruitment to sites of inflammation and infection …

DMD gene pathogenic variations cause a spectrum of phenotypes, ranging from severe
Duchenne muscular dystrophy, the Becker milder cases, the intermediate or very mild …

The Popeye domain–containing 1 (POPDC1) gene encodes a plasma membrane–localized
cAMP-binding protein that is abundantly expressed in striated muscle. In animal models …

Brugada syndrome (BrS) is an inherited cardiac channelopathy first diagnosed in 1992 but
still considered a challenging disease in terms of diagnosis, arrhythmia risk prediction …

Dystrophinopathies are inherited diseases caused by mutations in the dystrophin (DMD)
gene for which testing is mandatory for genetic diagnosis, reproductive choices and …

SERine Protein INhibitor-A1 (SERPINA1) is an inducible blood cell gene coding for alpha1-
antitrypsin (AAT), a plasma protease inhibitor whose circulating levels are raised during …

Abstract Background Although Duchenne and Becker muscular dystrophies, X-linked
recessive myopathies, predominantly affect males, a clinically significant proportion of …

Aberrant methylation at the H19 paternal imprinted gene has been identified in different
cohorts of infertile males. The causes of H19 methylation errors are poorly understood. In …

Purpose: The purpose of this investigation was to characterize Merkel cell carcinomas
(MCC) arisen in patients affected by autoimmune diseases and treated with biologic drugs …

To evaluate the gene expression changes involved in neoplastic progression of cervical
intraepithelial neoplasia. Using microarray analysis, large‐scale gene expression profile …