Juan Wang

Multiorgan engraftment and differentiation of human cord blood CD34+ Lin- cells in goats assessed by gene expression profiling.

In utero transplantation of human hematopoietic stem/progenitor cells partially repairs injured liver in mice.

Overexpressed epidermal growth factor receptor (EGFR)-induced progestin insensitivity in human endometrial carcinoma cells by the EGFR/mitogen-activated protein kinase signaling pathway.

Development of Polysorbate 80/Phospholipid mixed micellar formation for docetaxel and assessment of its in vivo distribution in animal models.

Measurement of mercury in flue gas based on an aluminum matrix sorbent.

Conversion of elemental mercury with a novel membrane catalytic system at low temperature.

Mercury removals by existing pollutants control devices of four coal-fired power plants in China.

Adjusting the attB site in donor plasmid improves the efficiency of ΦC31 integrase system.

Prevention and treatment of allergic inflammation by an Fcγ-Der f2 fusion protein in a murine model of dust mite-induced asthma.

Epidermal growth factor receptor signaling pathway involved in progestin-resistance of human endometrial carcinoma: In a mouse model.

Bacterial flora and extraradicular biofilm associated with the apical segment of teeth with post-treatment apical periodontitis.

Optimized preparation of celastrol-loaded polymeric nanomicelles using rotatable central composite design and response surface methodology.

Proteomic identification of PKM2 and HSPA5 as potential biomarkers for predicting high-risk endometrial carcinoma.

Adrenocorticotropic hormone ameliorates acute kidney injury by steroidogenic-dependent and -independent mechanisms.

Imaging of extraradicular biofilm using combined scanning electron microscopy and stereomicroscopy.

Decreased plasma apolipoprotein A-IV levels in patients with acute coronary syndrome.

PITX2c loss-of-function mutations responsible for congenital atrial septal defects.

GATA4 loss-of-function mutations underlie familial tetralogy of fallot.

A CLE-WOX signalling module regulates root meristem maintenance and vascular tissue development in rice.

[Establishment of the methodology for quantifying lentiviral vector transcriptional read-through rate].

Laboratory aspirin resistance and the risk of major adverse cardiovascular events in patients with coronary heart disease on confirmed aspirin adherence.

Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.

PhiC31 integrase induces efficient site-specific recombination in the Capra hircus genome.

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.

Interleukin-4 and interleukin-13 pathway genetics affect disease susceptibility, serum immunoglobulin E levels, and gene expression in asthma.

Cutaneous Vasculitis, Interstitial Pneumonia with Crazy-Paving Appearance, and Positive pANCA in a Patient with Severe Crohn's Disease.

A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve.

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.

GATA5 loss-of-function mutation in familial dilated cardiomyopathy.

TBX20 loss-of-function mutation contributes to double outlet right ventricle.

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Mutagenic Effects of Perfluorooctanesulfonic Acid in gpt Delta Transgenic System Are Mediated by Hydrogen Peroxide.

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

Compressing with dominant hand improves quality of manual chest compressions for rescuers who performed suboptimal CPR in manikins.

Pulsatility index in combination with biomarkers or mean arterial pressure for the prediction of pre-eclampsia: Systematic literature review and meta-analysis.

JNK is required for maintaining the tumor-initiating cell-like properties of acquired chemoresistant human cancer cells.

Performance of cardiopulmonary resuscitation during prolonged basic life support in military medical university students: A manikin study.

A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot.

A Novel Portable Foldable Laparoscopic Trainer for Surgical Education.

Genomic analyses reveal FAM84B and the NOTCH pathway are associated with the progression of esophageal squamous cell carcinoma.

Mast Cell-Derived Exosomes Promote Th2 Cell Differentiation via OX40L-OX40 Ligation.

Emodin enhances cisplatin-induced cytotoxicity in human bladder cancer cells through ROS elevation and MRP1 downregulation.

The human nucleophosmin 1 mutation A inhibits myeloid differentiation of leukemia cells by modulating miR-10b.

CASZ1 loss-of-function mutation associated with congenital heart disease.

Magnetically separable maghemite/montmorillonite composite as an efficient heterogeneous Fenton-like catalyst for phenol degradation.

HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.

Ratios of biochemical markers in peritoneal fluid to those in venous blood for the diagnosis of ruptured tubal pregnancy: A prospective study.

Adipogenic niches for melanoma cell colonization and growth in bone marrow.

Association between ErbB4 single nucleotide polymorphisms and susceptibility to schizophrenia: A meta-analysis of case-control studies.

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.

Evaluation of the potential of kartogenin encapsulated poly(L-lactic acid-co-caprolactone)/collagen nanofibers for tracheal cartilage regeneration.

Oral administration of curcumin attenuates visceral hyperalgesia through inhibiting phosphorylation of TRPV1 in rat model of ulcerative colitis.

Mast cell exosomes can suppress allergic reactions by binding to IgE.

Levels, sources and probabilistic health risks of polycyclic aromatic hydrocarbons in the agricultural soils from sites neighboring suburban industries in Shanghai.

MEF2C loss-of-function mutation contributes to congenital heart defects.

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.

TBX1 loss-of-function mutation contributes to congenital conotruncal defects.

Hydrogen Inhalation is Superior to Mild Hypothermia for Improving Neurological Outcome and Survival in a Cardiac Arrest Model of Spontaneously Hypertensive Rat.

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

The histone demethylase Jmjd3 regulates zebrafish myeloid development by promoting spi1 expression.

GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.

Nucleus accumbens controls wakefulness by a subpopulation of neurons expressing dopamine D receptors.

Enhancer of zeste homolog 2 blockade by RNA interference is implicated with inhibited proliferation, invasion and promoted apoptosis in endometrial carcinoma.

Identification of key biomarkers and immune infiltration in systemic lupus erythematosus by integrated bioinformatics analysis.

Correction to: Identification of key biomarkers and immune infiltration in systemic lupus erythematosus by integrated bioinformatics analysis.

EIF2AK2 selectively regulates the gene transcription in immune response and histones associated with systemic lupus erythematosus.

5-Aminolevulinic acid induced photodynamic therapy (ALA-PDT) for erosive adenomatosis of the nipple: a case report.