While the factors that regulate the onset and progression of idiopathic pulmonary fibrosis
(IPF) are incompletely understood, recent investigations have revealed that endoplasmic …

Idiopathic pulmonary fibrosis (IPF) is a life-threatening condition, with a median survival of<
3 yrs. The pathophysiology is not fully understood, but chronic injury of alveolar epithelial …

BACKGROUND AND OBJECTIVE: Neonatal respiratory distress syndrome (RDS) due to
pulmonary surfactant deficiency is heritable, but common variants do not fully explain …

Epithelial cell dysfunction is now recognized as an important mechanism in the
pathogenesis of interstitial lung diseases. Surfactant Protein C (SP-C), an alveolar type II cell …

The term “children's interstitial lung disease”(chILD) refers to a heterogeneous group of rare
and diffuse lung diseases associated with significant morbidity and mortality. These …

Цель исследования. Оценка генетической изменчивости вируса гриппа A НIN1"
пандемический"(ВГА НIN1" пан") в условиях эпидемии и обнаружение набора …

This chapter details the clinical presentation, pathophysiology, diagnosis, and management
of pulmonary alveolar proteinosis and lymphangioleiomyomatosis (LAM). It also highlights …

Tyrosine kinases (TKs) are key regulators of signal transduction pathways that modulate
essential biological processes, such as cellular differentiation, metabolism and proliferation …

Aim. To assess genetic variability of A H1N1 pan influenza virus (IV) in the course of the
epidemic and to detect a set of human nucleotide polymorphisms responsible for a severe …

A 65 years old farmer was admitted in Medicine ward with the complaints of progressive
exertional breathlessness, non-productive cough and recurrent episodes of fever. The …