Suchergebnisse - (Person:"Zhang, Min")

PubPharm (8)

1

Fibrillin-1 gene mutations in a Chinese cohort with congenital ectopia lentis : spectrum and genotype-phenotype analysis

enthalten in: The British journal of ophthalmology | 2022

von Chen, Z. | Chen, T. | Zhang, M. | +5

2

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

enthalten in: Clinical chemistry and laboratory medicine | 2021

von Qiao, Q. | Zhao, C. | Yang, C. | +7

3

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy

enthalten in: Genes | 2021

von Li, N. | Xu, Y. | Shi, H. | +6

4

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

enthalten in: Clinical chemistry and laboratory medicine | 2018

von Yuan, F. | Qiu, Z. | Wang, X. | +12

5

TBX1 loss-of-function mutation contributes to congenital conotruncal defects

enthalten in: Experimental and therapeutic medicine | 2018

von Zhang, M. | Li, F. | Liu, X. | +9

6

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

enthalten in: Clinical chemistry and laboratory medicine | 2017

von Qiu, X. | Qu, X. | Li, R. | +12

7

Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes

enthalten in: Circulation. Cardiovascular genetics | 2014

von Tao, Y. | Zhang, M. | Li, L. | +5

8

Gene network and proteomic analyses of cardiac responses to pathological and physiological stress

enthalten in: Circulation. Cardiovascular genetics | 2013

von Drozdov, I. | Didangelos, A. | Yin, X. | +8

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