X Wang

ORCID: 0009-0008-2620-9036
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About
Contact & Profiles
Research Areas
  • Education and Learning Interventions
  • Pediatric Hepatobiliary Diseases and Treatments
  • Genomics and Rare Diseases
  • Advanced MRI Techniques and Applications
  • Education and Critical Thinking Development
  • Ethics in Business and Education
  • Asthma and respiratory diseases
  • Psychosocial Factors Impacting Youth
  • Cardiac Imaging and Diagnostics
  • Medical Imaging Techniques and Applications
  • Bladder and Urothelial Cancer Treatments
  • Metabolism and Genetic Disorders
  • IL-33, ST2, and ILC Pathways
  • Values and Moral Education
  • Healthcare Education and Workforce Issues

UCSI University
2024

Shanghai Children's Hospital
2018-2023

Shanghai Jiao Tong University
2023

Asthma is a complex and heterogeneous disease. We found gene-gene interactions between IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, FCER1B rs569108 in asthmatic Chinese Han children. This 4-locus set constituted an optimal statistical interaction model. examined associations the 4-gene model (IL13, IL4, FCER1B, ADRB2) Predictive Index (API) atopy children.Four single-nucleotide polymorphisms 4 genes were genotyped 385 preschool children with wheezing symptoms using matrix-assisted laser...

10.18176/jiaci.0272 article EN Journal of Investigational Allergology and Clinical Immunology 2018-05-15

Introduction: This study was to develop A Scale of Professional Ethical Dilemma for Teachers and verified the reliability validity questionnaire, provide an objective effective measurement tool evaluation professional ethics dilemma teachers. It may empirical research teachers' ethical dilemmas scientifically assess level dilemmas.Methods: used literature review teachers interview select contents did pilot test expert judgment form experimental version scale.Results: developed a scale...

10.56294/sctconf2024.1252 article EN cc-by Salud Ciencia y Tecnología - Serie de Conferencias 2024-10-16

患儿 女,18月龄,因“新型冠状病毒核酸筛查异常2 d”入上海交通大学医学院附属仁济医院(南部院区)定点医院隔离病房。患儿表现为特殊面容,发育迟缓,且因先天性胆道闭锁及腭裂先后行肝移植手术及腭裂修复术,为进一步明确病因,故行全外显子基因检测提示KMT2D基因杂合变异,变异位点为exon39:c.11965C>T(p.Q3989X),结合患儿临床表现和基因结果确诊为歌舞伎综合征。.

10.3760/cma.j.cn112140-20220704-00613 article ZH-CN PubMed 2023-02-02

10.52152/kuey.v30i2.743 article EN Educational Administration Theory and Practice journal 2023-12-25
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