Yongchen Yang

ORCID: 0000-0001-7063-6707
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About
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Research Areas
  • Acute Myeloid Leukemia Research
  • RNA and protein synthesis mechanisms
  • Cardiomyopathy and Myosin Studies
  • Muscle Physiology and Disorders
  • Helicobacter pylori-related gastroenterology studies
  • RNA modifications and cancer
  • Cancer-related molecular mechanisms research
  • Neurogenetic and Muscular Disorders Research
  • Microscopic Colitis
  • Chronic Myeloid Leukemia Treatments
  • Gastric Cancer Management and Outcomes
  • Clostridium difficile and Clostridium perfringens research
  • Acute Lymphoblastic Leukemia research
  • Metastasis and carcinoma case studies
  • Biomarkers in Disease Mechanisms
  • Gastrointestinal motility and disorders
  • Hematological disorders and diagnostics
  • Immune Response and Inflammation

Shanghai Children's Hospital
2014-2023

Shanghai Jiao Tong University
2023

Fudan University
2007-2018

Institute of Forensic Science
2018

Shanghai Public Security Bureau
2018

Lanzhou University
2008

First Hospital of Lanzhou University
2008

Abstract Both Duchenne muscular dystrophy (DMD; OMIM no. 310200) and spinal atrophy (SMA; 253300/253550/253400/271150) are genetic disorders characterized by progressive muscle degeneration weakness. Genetic copy number aberrations in the pathogenetic genes DMD SMN1 lead to alterations functional proteins, resulting SMA, respectively. Multiplex ligation-dependent probe amplification (MLPA) has become a standard method for detection of common (CNAs), including deletions, both which associated...

10.1007/s12035-023-03572-9 article EN cc-by Molecular Neurobiology 2023-08-19

Background.Pseudomembranous enteritis (PME) is an acute inflammatory bowel disease affecting pediatric population.The aim of this study was to discuss the characteristics, diagnosis, and management PME, potential possibility fecal microbiota transplantation (FMT) application in PME.Methods.The clinical manifestations, laboratory testing, treatment one case with severe PME were reviewed, analyzed, summarized.Meanwhile, associated literatures FMT reviewed article.

10.1093/ofid/ofu052.1202 article EN cc-by-nc-nd Open Forum Infectious Diseases 2014-01-01

To analyse and detect CSF1PO D18S51 loci by next generation sequencing (NGS) technology for the study on their sequence polymorphism.The peripheral blood samples were collected from 165 unrelated individuals of Chinese Han population. DNA obtained QIAamp Mini kit. The library was constructed Ion Plus Fragment Library. analysis performed Torrent PGM™ Platform. newfound alleles verified Sanger sequencing. Data analysed Suite™ v5.0.2 Integrative Genomics Viewer genotype identification frequency...

10.12116/j.issn.1004-5619.2018.05.017 article EN PubMed 2018-10-01
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