W. Lai

发表

The L-shaped association between superoxide dismutase levels and blood pressure in older Chinese adults: community-based, cross-sectional study

Qifang Liu, Jin-zhu Hu, Ju-xiang Li, 2022, Journal of geriatric cardiology : JGC.

A novel KRT5 mutation, p.Lys199Asn, is associated with three subtypes of epidermolysis bullosa simplex phenotypes in a single Chinese family.

Yiming Wang, P. Yuan, Weiping Deng, 2011, Journal of dermatological science.

Ubiquitin-like protein FAT10 suppresses SIRT1-mediated autophagy to protect against ischemic myocardial injury.

J. Shao, K. Hong, Jinyan Xie, 2020, Journal of molecular and cellular cardiology.

Evaluation of a Potential Clinical Signif icant Drug-Drug I n t e r a c t i o n b e

Yang Shen, Aizhen Xiong, Xijing Chen, 2018 .

Evaluation of a Potential Clinical Significant Drug-Drug Interaction between Digoxin and Bupropion in Cynomolgus Monkeys

K. Hong, Yang Shen, Xijing Chen, 2018, Pharmaceutical Research.

A recurrent p. A353V mutation in DKC1 responsible for different phenotypes of dyskeratosis congenita in a Chinese family.

H. M. Chen, W. Lai, Sh X Dai, 2011, Journal of dermatological science.

Chaperone‐mediated autophagy attenuates H2O2‐induced cardiomyocyte apoptosis by targeting poly (ADP‐ribose) polymerase 1 (PARP1) for lysosomal degradation

Yang Liu, Yang Shen, R. Wan, 2022, Cell biology international.

The safety of morphine in patients with acute heart failure: A systematic review and meta‐analysis

K. Hong, Yang Shen, Xiao Liu, 2021, Clinical cardiology.

A novel p.Gly1700Asp mutation in COL7A1 responsible for dominant dystrophic epidermolysis bullosa: more severe phenotype in female members of a Chinese family.

Xiaoping Zhou, Bin Hu, Yiming Wang, 2008, Journal of dermatological science.

Genotype-based clinical manifestation and treatment of Chinese long QT syndrome patients with KCNQ1 mutations – R380S and W305L

K. Hong, Jinyan Xie, Y. Liu, 2015, Cardiology in the Young.