Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ye Zheng"'
Autor:
Bin Li, Wen-Xuan Sun, Wan-Ying Zhang, Ye Zheng, Lu Qiao, Yue-Ming Hu, Wei-Qiang Li, Di Liu, Bing Leng, Jia-Ren Liu, Xiao-Feng Jiang, Yan Zhang
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Rationale: Severe asthma is a heterogeneous disease with multiple molecular mechanisms. Gene expression studies of asthmatic bronchial epithelial cells have provided biological insights and underscored possible pathological mechanisms; however, the m
Publikováno v:
Molecular Medicine Reports
The present study aimed to investigate the expression of microRNA (miR)-133a in patients with or without acute myocardial infarction (AMI) following radical surgery for gastric cancer, and to explore its underlying mechanisms. Blood samples were coll
Autor:
Qiongshi Lu, Kunling Huang, Sushmita Roy, Junha Shin, Daifeng Wang, Yuchang Wu, Zheng Ni, Jing You, Sunduz Keles, Yupei Lin, Ye Zheng, Alireza Fotuhi Siahpirani, Jiawen Chen
Publikováno v:
PLoS Genetics, Vol 17, Iss 2, p e1009309 (2021)
PLoS Genetics
PLoS Genetics
Recent advances in consortium-scale genome-wide association studies (GWAS) have highlighted the involvement of common genetic variants in autism spectrum disorder (ASD), but our understanding of their etiologic roles, especially the interplay with ra
Autor:
R. Gada, Gary L. Keeney, Raul Urrutia, Zaid M. Tabbaa, Angela Mathison, Adrienne Grzenda, John K. Schoolmeester, Gaurang S. Daftary, Ye Zheng, Gwen Lomberk
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e60165 (2013)
PLoS ONE
PLoS ONE
Endometriosis affects approximately 10% of young, reproductive-aged women. Disease associated pelvic pain; infertility and sexual dysfunction have a significant adverse clinical, social and financial impact. As precise disease etiology has remained e
Autor:
Cong Tian, Fengchan Han, Ye Zheng, Heping Yu, Bin Yang, Cynthia F. Bartels, Peter C. Scacheri, Deborah K. Schelling, Qing Yin Zheng, James E. Arnold
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e34944 (2012)
PLoS ONE
PLoS ONE
Otitis media is a middle ear disease common in children under three years old. Otitis media can occur in normal individuals with no other symptoms or syndromes, but it is often seen in individuals clinically diagnosed with genetic diseases such as CH
Autor:
Bin Yang, Rami Azem, Cong Tian, Ge Jin, Qing Yin Zheng, Feng chan Han, Ye Zheng, Heping Yu, Zhi guang Zhang, James E. Arnold
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 7, p e22622 (2011)
PLoS ONE, Vol 6, Iss 7, p e22622 (2011)
Craniofacial defects that occur through gene mutation during development increase vulnerability to eustachian tube dysfunction. These defects can lead to an increased incidence of otitis media. We examined the effects of a mutation in the Sh3pxd2b ge