Congenital heart defects (CHDs) refer to abnormalities in the heart function that arise at the
fetal stages. It is the most common birth defect that affects 0.8% of all liveborn infants. There …

At present, epigenetic markers have been extensively studied in various fields and have a
high value in forensic medicine due to their unique mode of inheritance, which does not …

Women undergoing infertility treatment are routinely subjected to one or more tests of
ovarian reserve. Therefore, an adequate assessment of the ovarian reserve is necessary for …

A six-fold increase in congenital heart defects (CHD) exists among monochorionic (MC)
twins compared to singleton or dichorionic twin pregnancies. Though MC twins share an …

Background Turner syndrome (TS) is a chromosomal disorder, in which a female is partially
or entirely missing one of the two X chromosomes, with a prevalence of 1: 2500 live female …

Bone morphogenetic protein receptor type-1B (BMPR1B) is one of the major gene for sheep
prolificacy. However, few studies investigated its regulatory region. In this study, we reported …

Congenital heart defects (CHDs) are the most common birth defect in human with an
incidence of almost 1% of all live births. Most cases have a multifactorial origin with both …

Aim: MicroRNAs (miRNAs) have been shown to play an important role in the progression of
heart failure (HF). The aim of our study was to analyze miRNAs in the blood of patients with …

Anthracyclines are widely used in the treatment of many solid cancers, but their efficacy is
limited by cardiotoxicity. As the number of pediatric cancer survivors continues to rise, there …

Little is known about abundance level changes of circulating microRNAs (miRNAs) and
messenger RNAs (mRNA) in patients with Ebstein's anomaly (EA). Here, we performed an …