Search Results - "Wang, Leitong"
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Homocysteine downregulates cardiac homeobox transcription factor NKX2.5 via IGFBP5
Published in American journal of physiology. Heart and circulatory physiology (01-12-2020)“…Homocysteine (Hcy) is an independent risk factor of congenital heart disease (CHD), but its exact underlying mechanism is unclear. In this study, we collected…”
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cMyBP-C was decreased via KLHL3-mediated proteasomal degradation in congenital heart diseases
Published in Experimental cell research (01-06-2017)“…Cardiac myosin binding protein C (cMyBP-C) is a cardiac structural and regulatory protein; mutations of cMyBP-C are frequently associated with hypertrophic…”
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Role of Nkx2.5 in H₂O₂-induced Nsd1 suppression
Published in Cell stress & chaperones (01-07-2019)“…Nuclear receptor–binding SET domain–containing protein 1 (Nsd1) acts as a histone lysine methyltransferase, and its role in oxidative stress–related abnormal…”
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Influence of Long Non-Coding RNAs on Human Oocyte Development
Published in Pharmacogenomics and personalized medicine (31-07-2024)“…Recent research findings have highlighted the pivotal roles played by lncRNAs in both normal human development and disease pathogenesis. LncRNAs are expressed…”
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miR-137 downregulates c-kit expression in acute myeloid leukemia
Published in Leukemia research (01-06-2017)“…Highlights • miR-137 targets the 3′-UTR of c-kit.. • miR-137 suppresses the expression and activities of c-kit in AML cell. • Expression of miR-137 inversely…”
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Role of Nkx2.5 in H 2 O 2 -induced Nsd1 suppression
Published in Cell stress & chaperones (01-07-2019)“…Nuclear receptor-binding SET domain-containing protein 1 (Nsd1) acts as a histone lysine methyltransferase, and its role in oxidative stress-related abnormal…”
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Decreased Amino Acid Concentrations are Involved in Congenital Heart Disease
Published in Annals of nutrition and metabolism (01-01-2019)“…Congenital heart disease (CHD) is the most common malformation in China. In this study, we determined whether amino acids (AAs) in the amniotic fluid (AF) of…”
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Differences in IGF axis-related proteins in amniotic fluid of trisomy 21 and trisomy 18 using a multiple reaction monitoring approach
Published in Prenatal diagnosis (01-12-2014)“…ABSTRACT Objective Trisomy 21 and trisomy 18 are the two most common chromosomal anomalies in live births. To find new biomarkers for aneuploidies and…”
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