Juan Wang

Juan Wang

Department of Rheumatology, Shanghai Jiao Tong University

Affiliated withShanghai Jiao Tong UniversityThird Military Medical University

Research Area

Cancer Research

Biography

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JoVE Journal Publications

ArticleTotal : 2
Year
Dual Effects of Melanoma Cell-derived Factors on Bone Marrow Adipocytes Differentiation
Publication title
2018
2021

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
2006
2010
2011
2011
2012
2011
2012
2012
2012
2012
2012
2013
2013
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
2013
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
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
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
2014
2014
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
2015
2015
2015
2015
2015
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
2016
2016
2016
2016
2016
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
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
2017
2017
2017
2017
Mast cell exosomes can suppress allergic reactions by binding to IgE.

The Journal of allergy and clinical immunology| PubMed ID: 28916187

2018
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
2018
GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

The American journal of cardiology| PubMed ID: 29325903

2018
2018
2018
2018
2018
2021
2021
2021
2021