Juan Wang

Department of Obstetrics and Gynecology, Huazhong University of Science and Technology

Affiliated withHuazhong University of Science and Technology

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2026

Other Publications

Article	Year
Multiorgan engraftment and differentiation of human cord blood CD34+ Lin- cells in goats assessed by gene expression profiling. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 16682618	2006
In utero transplantation of human hematopoietic stem/progenitor cells partially repairs injured liver in mice. International journal of molecular medicine\| PubMed ID: 16964416	2006
Overexpressed epidermal growth factor receptor (EGFR)-induced progestin insensitivity in human endometrial carcinoma cells by the EGFR/mitogen-activated protein kinase signaling pathway. Cancer\| PubMed ID: 20564127	2010
Development of Polysorbate 80/Phospholipid mixed micellar formation for docetaxel and assessment of its in vivo distribution in animal models. Nanoscale research letters\| PubMed ID: 21711889	2011
Measurement of mercury in flue gas based on an aluminum matrix sorbent. TheScientificWorldJournal\| PubMed ID: 22235178	2011
Conversion of elemental mercury with a novel membrane catalytic system at low temperature. Journal of hazardous materials\| PubMed ID: 22341492	2012
Mercury removals by existing pollutants control devices of four coal-fired power plants in China. Journal of environmental sciences (China)\| PubMed ID: 22432308	2011
Adjusting the attB site in donor plasmid improves the efficiency of ΦC31 integrase system. DNA and cell biology\| PubMed ID: 22489575	2012
Prevention and treatment of allergic inflammation by an Fcγ-Der f2 fusion protein in a murine model of dust mite-induced asthma. Immunologic research\| PubMed ID: 22539132	2012
Epidermal growth factor receptor signaling pathway involved in progestin-resistance of human endometrial carcinoma: In a mouse model. The journal of obstetrics and gynaecology research\| PubMed ID: 22612393	2012
Bacterial flora and extraradicular biofilm associated with the apical segment of teeth with post-treatment apical periodontitis. Journal of endodontics\| PubMed ID: 22703660	2012
Optimized preparation of celastrol-loaded polymeric nanomicelles using rotatable central composite design and response surface methodology. Journal of biomedical nanotechnology\| PubMed ID: 22764419	2012
Proteomic identification of PKM2 and HSPA5 as potential biomarkers for predicting high-risk endometrial carcinoma. The journal of obstetrics and gynaecology research\| PubMed ID: 22889453	2013
Adrenocorticotropic hormone ameliorates acute kidney injury by steroidogenic-dependent and -independent mechanisms. Kidney international\| PubMed ID: 23325074	2013
Imaging of extraradicular biofilm using combined scanning electron microscopy and stereomicroscopy. Microscopy research and technique\| PubMed ID: 23857917	2013
Decreased plasma apolipoprotein A-IV levels in patients with acute coronary syndrome. Clinical and investigative medicine. Medecine clinique et experimentale\| PubMed ID: 23906492	2013
PITX2c loss-of-function mutations responsible for congenital atrial septal defects. International journal of medical sciences\| PubMed ID: 23983605	2013
GATA4 loss-of-function mutations underlie familial tetralogy of fallot. Human mutation\| PubMed ID: 24000169	2013
A CLE-WOX signalling module regulates root meristem maintenance and vascular tissue development in rice. Journal of experimental botany\| PubMed ID: 24043854	2013
[Establishment of the methodology for quantifying lentiviral vector transcriptional read-through rate]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology\| PubMed ID: 24195367	2013
Laboratory aspirin resistance and the risk of major adverse cardiovascular events in patients with coronary heart disease on confirmed aspirin adherence. Journal of atherosclerosis and thrombosis\| PubMed ID: 24201035	2014
Novel PITX2c loss-of-function mutations associated with complex congenital heart disease. International journal of molecular medicine\| PubMed ID: 24604414	2014
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve. International journal of molecular medicine\| PubMed ID: 24638895	2014
PhiC31 integrase induces efficient site-specific recombination in the Capra hircus genome. DNA and cell biology\| PubMed ID: 24754538	2014
Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation. International journal of medical sciences\| PubMed ID: 24782644	2014
Interleukin-4 and interleukin-13 pathway genetics affect disease susceptibility, serum immunoglobulin E levels, and gene expression in asthma. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology\| PubMed ID: 24980391	2014
Cutaneous Vasculitis, Interstitial Pneumonia with Crazy-Paving Appearance, and Positive pANCA in a Patient with Severe Crohn's Disease. Case reports in gastrointestinal medicine\| PubMed ID: 25371834	2014
A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve. The American journal of cardiology\| PubMed ID: 25438918	2014
A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias. International journal of molecular medicine\| PubMed ID: 25503402	2015
GATA5 loss-of-function mutation in familial dilated cardiomyopathy. International journal of molecular medicine\| PubMed ID: 25543888	2015
TBX20 loss-of-function mutation contributes to double outlet right ventricle. International journal of molecular medicine\| PubMed ID: 25625280	2015
TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy. Biochemical and biophysical research communications\| PubMed ID: 25725155	2015
Mutagenic Effects of Perfluorooctanesulfonic Acid in gpt Delta Transgenic System Are Mediated by Hydrogen Peroxide. Environmental science & technology\| PubMed ID: 25875360	2015
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome. PloS one\| PubMed ID: 25893250	2015
Compressing with dominant hand improves quality of manual chest compressions for rescuers who performed suboptimal CPR in manikins. The American journal of emergency medicine\| PubMed ID: 25937378	2015
Pulsatility index in combination with biomarkers or mean arterial pressure for the prediction of pre-eclampsia: Systematic literature review and meta-analysis. Annals of medicine\| PubMed ID: 26153822	2015
JNK is required for maintaining the tumor-initiating cell-like properties of acquired chemoresistant human cancer cells. Acta pharmacologica Sinica\| PubMed ID: 26235742	2015
Performance of cardiopulmonary resuscitation during prolonged basic life support in military medical university students: A manikin study. World journal of emergency medicine\| PubMed ID: 26401177	2015
A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot. International journal of molecular medicine\| PubMed ID: 26676105	2016
A Novel Portable Foldable Laparoscopic Trainer for Surgical Education. Journal of surgical education\| PubMed ID: 26700974	2016
Genomic analyses reveal FAM84B and the NOTCH pathway are associated with the progression of esophageal squamous cell carcinoma. GigaScience\| PubMed ID: 26759717	2016
Mast Cell-Derived Exosomes Promote Th2 Cell Differentiation via OX40L-OX40 Ligation. Journal of immunology research\| PubMed ID: 27066504	2016
Emodin enhances cisplatin-induced cytotoxicity in human bladder cancer cells through ROS elevation and MRP1 downregulation. BMC cancer\| PubMed ID: 27485374	2016
The human nucleophosmin 1 mutation A inhibits myeloid differentiation of leukemia cells by modulating miR-10b. Oncotarget\| PubMed ID: 27669739	2016
CASZ1 loss-of-function mutation associated with congenital heart disease. Gene\| PubMed ID: 27693370	2016
Magnetically separable maghemite/montmorillonite composite as an efficient heterogeneous Fenton-like catalyst for phenol degradation. Environmental science and pollution research international\| PubMed ID: 27798800	2017
HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot. Pediatric cardiology\| PubMed ID: 27942761	2017
HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle. International journal of molecular medicine\| PubMed ID: 28112363	2017
Ratios of biochemical markers in peritoneal fluid to those in venous blood for the diagnosis of ruptured tubal pregnancy: A prospective study. European journal of obstetrics, gynecology, and reproductive biology\| PubMed ID: 28157643	2017
Adipogenic niches for melanoma cell colonization and growth in bone marrow. Laboratory investigation; a journal of technical methods and pathology\| PubMed ID: 28218738	2017
Association between ErbB4 single nucleotide polymorphisms and susceptibility to schizophrenia: A meta-analysis of case-control studies. Medicine\| PubMed ID: 28225484	2017
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. International journal of medical sciences\| PubMed ID: 28553164	2017
Evaluation of the potential of kartogenin encapsulated poly(L-lactic acid-co-caprolactone)/collagen nanofibers for tracheal cartilage regeneration. Journal of biomaterials applications\| PubMed ID: 28658997	2017
Oral administration of curcumin attenuates visceral hyperalgesia through inhibiting phosphorylation of TRPV1 in rat model of ulcerative colitis. Molecular pain\| PubMed ID: 28812431	2017
Mast cell exosomes can suppress allergic reactions by binding to IgE. The Journal of allergy and clinical immunology\| PubMed ID: 28916187	2018
Levels, sources and probabilistic health risks of polycyclic aromatic hydrocarbons in the agricultural soils from sites neighboring suburban industries in Shanghai. The Science of the total environment\| PubMed ID: 29074242	2018
MEF2C loss-of-function mutation contributes to congenital heart defects. International journal of medical sciences\| PubMed ID: 29104469	2017
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect. European journal of medical genetics\| PubMed ID: 29222010	2018
TBX1 loss-of-function mutation contributes to congenital conotruncal defects. Experimental and therapeutic medicine\| PubMed ID: 29250159	2018
Hydrogen Inhalation is Superior to Mild Hypothermia for Improving Neurological Outcome and Survival in a Cardiac Arrest Model of Spontaneously Hypertensive Rat. Shock (Augusta, Ga.)\| PubMed ID: 29280927	2018
GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve. The American journal of cardiology\| PubMed ID: 29325903	2018
The histone demethylase Jmjd3 regulates zebrafish myeloid development by promoting spi1 expression. Biochimica et biophysica acta\| PubMed ID: 29378332	2018
GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve. Gene\| PubMed ID: 29653232	2018
Nucleus accumbens controls wakefulness by a subpopulation of neurons expressing dopamine D receptors. Nature communications\| PubMed ID: 29679009	2018
Enhancer of zeste homolog 2 blockade by RNA interference is implicated with inhibited proliferation, invasion and promoted apoptosis in endometrial carcinoma. Oncology letters\| PubMed ID: 29805666	2018
Identification of key biomarkers and immune infiltration in systemic lupus erythematosus by integrated bioinformatics analysis. Journal of translational medicine\| PubMed ID: 33468161	2021
Correction to: Identification of key biomarkers and immune infiltration in systemic lupus erythematosus by integrated bioinformatics analysis. Journal of translational medicine\| PubMed ID: 33573651	2021
EIF2AK2 selectively regulates the gene transcription in immune response and histones associated with systemic lupus erythematosus. Molecular immunology\| PubMed ID: 33588244	2021
5-Aminolevulinic acid induced photodynamic therapy (ALA-PDT) for erosive adenomatosis of the nipple: a case report. Photodiagnosis and photodynamic therapy\| PubMed ID: 34107318	2021