Suchergebnisse - "Wang, Pengyun"

PubPharm (36)

1

Gene polymorphism in IL17A and gene-gene interaction in the IL23R/IL17A axis are associated with susceptibility to coronary artery disease

enthalten in: Cytokine | 2023

von Zhang, H. | Nie, S. | Chen, Q. | +6

2

Hepatocyte Ninjurin2 promotes hepatic stellate cell activation and liver fibrosis through the IGF1R/EGR1/PDGF-BB signaling pathway

enthalten in: Metabolism: clinical and experimental | 2023

von Wang, Y. | Wang, P. | Yu, Y. | +13

3

Association of ApoE gene polymorphisms with serum lipid levels and the risk of type 2 diabetes mellitus in the Chinese Han population of central China

enthalten in: PeerJ | 2023

von Zeng, Y. | Wen, S. | Huan, L. | +3

4

NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling

enthalten in: Obesity (Silver Spring, Md.) | 2023

von Peng, H. | Yu, Y. | Wang, P. | +12

5

Functional rare variant in a C/EBPbeta binding site in NINJ2 gene increases the risk of coronary artery disease

enthalten in: Aging | 2021

von Wang, P. | Wang, Y. | Peng, H. | +11

6

Human Leukocyte Antigen Profile Predicts Severity of Autoimmune Liver Disease in Children of European Ancestry

enthalten in: Hepatology (Baltimore, Md.) | 2021

von Ma, Y. | Su, H. | Yuksel, M. | +16

7

SNP rs2243828 in MPO associated with myeloperoxidase level and atrial fibrillation risk in Chinese Han population

enthalten in: Journal of cellular and molecular medicine | 2020

von Wang, P. | Cheng, M. | Wang, P. | +9

8

Subjective well-being is associated with the functional connectivity network of the dorsal anterior insula

enthalten in: Neuropsychologia | 2020

von Li, R. | Zhu, X. | Zheng, Z. | +2

9

Study of reference intervals for free triiodothyronine, free thyroxine, and thyroid-stimulating hormone in an elderly Chinese Han population

enthalten in: PloS one | 2020

von Xiong, J. | Liu, S. | Hu, K. | +3

ErratumIn: PLoS One. 2021 Jun 10;16(6):e0253359. - PMID 34111234

10

Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillation

enthalten in: Annals of human genetics | 2019

von Xiong, H. | Yang, Q. | Zhang, X. | +28