Search Results - "Ma, Duan"
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A Lancet Commission on 70 years of women's reproductive, maternal, newborn, child, and adolescent health in China
Published in The Lancet (British edition) (26-06-2021)“…According to this strategic framework, we have put forward a series of five broad recommendations, covering reproductive health, maternal and newborn health,…”
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Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients
Published in PloS one (16-01-2013)“…Velocardiofacial syndrome (VCFS) is a disease in human with an expansive phenotypic spectrum and diverse genetic mechanisms mainly associated with copy number…”
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3
Fasting inhibits aerobic glycolysis and proliferation in colorectal cancer via the Fdft1-mediated AKT/mTOR/HIF1α pathway suppression
Published in Nature communications (20-04-2020)“…Evidence suggests that fasting exerts extensive antitumor effects in various cancers, including colorectal cancer (CRC). However, the mechanism behind this…”
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4
Recent advances in the epigenetics of bone metabolism
Published in Journal of bone and mineral metabolism (01-11-2021)“…Osteoporosis is a common form of metabolic bone disease that is costly to treat and is primarily diagnosed on the basis of bone mineral density. As the…”
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m6A Modification: A Double-Edged Sword in Tumor Development
Published in Frontiers in oncology (26-07-2021)“…Modification of m6A, as the most abundant mRNA modification, plays diverse roles in various biological processes in eukaryotes. Emerging evidence has revealed…”
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Downregulation of MEG3 and upregulation of EZH2 cooperatively promote neuroblastoma progression
Published in Journal of cellular and molecular medicine (01-04-2022)“…Neuroblastoma (NB), an embryonic tumour originating from sympathetic crest cells, is the most common extracranial solid tumour type in children with poor…”
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The induction of microRNA targeting IRS-1 is involved in the development of insulin resistance under conditions of mitochondrial dysfunction in hepatocytes
Published in PloS one (25-03-2011)“…Mitochondrial dysfunction induces insulin resistance in myocytes via a reduction of insulin receptor substrate-1 (IRS-1) expression. However, the effect of…”
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Modulation of Unregulated Inflammation‐Associated Coagulopathy in Sepsis Using Multifunctional Nanosheets
Published in Advanced functional materials (01-09-2024)“…Excessive inflammation‐associated unregulated coagulation leads to disseminated intravascular coagulation (DIC) and mortality in patients with sepsis…”
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Identification of an autophagy-related gene signature predicting overall survival for hepatocellular carcinoma
Published in Bioscience reports (29-01-2021)“…The poor prognosis of hepatocellular carcinoma (HCC) calls for the development of accurate prognostic models. The growing number of studies indicating a…”
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10
Trophoblast Exosomal UCA1 Induces Endothelial Injury through the PFN1-RhoA/ROCK Pathway in Preeclampsia: A Human-Specific Adaptive Pathogenic Mechanism
Published in Oxidative medicine and cellular longevity (15-09-2022)“…Preeclampsia is regarded as an evolution-related disease that has only been observed in humans and our closest relatives, and the important factor contributing…”
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DNA methylation status of TBX20 in patients with tetralogy of Fallot
Published in BMC medical genomics (28-05-2019)“…TBX20 plays an important role in heart development; however, its epigenetic regulation in the pathogenesis of tetralogy of Fallot (TOF) remains unclear. The…”
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DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome
Published in Scientific reports (30-04-2019)“…Congenital heart diseases (CHDs) are the most common types of birth defects, affecting approximately 1% of live births and remaining the leading cause of…”
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Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
Published in Journal of cellular and molecular medicine (01-06-2020)“…Tetralogy of Fallot (TOF) is the most common complex congenital heart disease (CHD) with uncertain cause. Although long non‐coding RNAs (lncRNAs) have been…”
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ARID1B/SUB1‐activated lncRNA HOXA‐AS2 drives the malignant behaviour of hepatoblastoma through regulation of HOXA3
Published in Journal of cellular and molecular medicine (01-04-2021)“…It has been becoming increasingly evident that long non‐coding RNAs (lncRNAs) play important roles in various human cancers. However, the biological processes…”
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Morphine promotes tumorigenesis and cetuximab resistance via EGFR signaling activation in human colorectal cancer
Published in Journal of cellular physiology (01-06-2021)“…Morphine, a mu‐opioid receptor (MOR) agonist, has been extensively used to treat advanced cancer pain. In particular, in patients with cancer metastasis, both…”
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Comprehensive expression profiling of microRNAs in laryngeal squamous cell carcinoma
Published in Head & neck (01-05-2013)“…Background MicroRNAs (miRNAs) are noncoding RNAs involved in posttranscriptional regulation of gene expression in cancer and provide new perspectives on the…”
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Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy
Published in Journal of medical genetics (01-02-2022)“…Nephronophthisis-related ciliopathies (NPHP-RC) account for the majority of cases of monogenetically caused end-stage renal disease (ESRD) in children…”
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The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish
Published in PLoS genetics (15-08-2018)“…SMYD4 belongs to a family of lysine methyltransferases. We analyzed the role of smyd4 in zebrafish development by generating a smyd4 mutant zebrafish line…”
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SLC34A2 simultaneously promotes papillary thyroid carcinoma growth and invasion through distinct mechanisms
Published in Oncogene (26-03-2020)“…Thyroid cancer is the fastest growing cancer among all solid tumors in recent decades. Papillary thyroid carcinoma (PTC) is the most predominant type of…”
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Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss
Published in Clinical genetics (01-10-2019)“…Hereditary non‐syndromic hearing loss is the most common inherited sensory defect in humans. More than 40 genes have been identified as causative genes for…”
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