Wilson's disease (WD) is an autosomal recessive disease caused by a mutation of the ATP7B
gene, resulting in abnormal copper metabolism. The major clinical features of WD include …

Turner syndrome (TS), also known as Congenital ovarian hypoplasia syndrome, occurs
when the X chromosome is partially or completely missing in females. Its main clinical …

Methylmalonic acidemia (MMA) is a lethal, severe heterogeneous disorder of methylmalonate
and cobalamin (cbl; vitamin B12) metabolism with poor prognosis. Two main forms of the …

… Yazhou Cui and Jinxiang Han were responsible for the study design and writing of the
manuscript. Yazhou Cui and Jing Luan were responsible for most of the experiments and the data …

The purpose of this study was to investigate the distribution of CD34-positive fibroblasts and
α-smooth muscle actin (α-SMA)-reactive myofibroblasts in the stroma of benign and …

Background Currently, early diagnosis of diabetic nephropathy (DN) remains a major
challenge. Thus, more investigations into new DN‐related biomarkers are needed. Methods We …

Many regulators have been identified to participate in the cross-talk between muscle and
bone, however, most previous studies focus on secreting proteins. In this study, we …

Objective. A proteomic approach was applied to discover novel rheumatoid arthritis (RA)-specific
proteins by comparing the expression profiles of synovial membranes from patients …

Amyotrophic Lateral Sclerosis (ALS) is a muscle-bone degenerative disease, which lacks a
specific index for diagnosis. In our previous studies, we found that exosomes mediated the …

Epidemiological information of hereditary spherocytosis in China is slight. This systematic
review summarizes the number of cases of hereditary spherocytosis reported in China Biology …