Suchergebnisse - "Wang, Pengyun"

PubPharm (9)

1

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

2

UBC9 regulates cardiac sodium channel Nav1.5 ubiquitination, degradation and sodium current density

enthalten in: Journal of molecular and cellular cardiology | 2019

von Tang, B. | Hu, Y. | Wang, Z. | +8

3

Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation

enthalten in: Scientific reports | 2018

von Wang, P. | Qin, W. | Wang, P. | +25

4

Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population

enthalten in: PloS one | 2015

von Wang, P. | Xu, C. | Wang, C. | +12

5

Reduced late positivity in younger adults, but not older adults, during short-term repetition

enthalten in: Brain research | 2015

von Zhou, T. | Li, J. | Broster, L. | +2

6

Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery disease

enthalten in: Circulation. Cardiovascular genetics | 2014

von Xu, C. | Yang, Q. | Xiong, H. | +36

CommentIn: Circ Cardiovasc Genet. 2014 Dec;7(6):738-40. - PMID 25516622

7

Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

enthalten in: Human genetics | 2011

von Li, C. | Wang, F. | Yang, Y. | +22

8

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population

enthalten in: Biochemical and biophysical research communications | 2010

von Wang, P. | Yang, Q. | Wu, X. | +17

9

Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family

enthalten in: BMC medical genetics | 2008

von Zhang, S. | Yin, K. | Ren, X. | +7

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