RATIONALE: Idiopathic pulmonary fibrosis (IPF) is a highly heterogeneous and lethal pathological process with limited therapcutic options, which is the most
p38 mitogen-activated protein kinase (MAPK) activity has been reported to either promote or suppress cell death, which depends on cell type and stimulus.
Objective: Mutations in gone ZBTB24 lead to autosomal-recessive immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome in some patie
Background: Group 2 innate lymphoid cells (ILC2s) are considered to be the most significant mediators during the orchestration of immune responses in asthma
Rationale: Severe combined immunodeficiency (SCID), a rare PID, is poorly characterized in China.We retrospectively reviewed patients with SCID refered to o