E-LIB Suche - Ergebnisse für: Dai, Rufeng

1

GEN1 as a risk factor for human congenital anomalies of the..:

Du, Xuanjin ; Wang, Chunyan ; Liu, Jialu...
Human Genomics. 18 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

Angiopoietin-like protein 3: a novel potential biomarker fo..:

Wen, Fujie ; Liu, Junchao ; Dai, Rufeng...
Frontiers in Pediatrics. 11 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

3

Copy Number Variation Analysis Facilitates Identification o..:

Wu, Chen-Han Wilfred ; Lim, Tze Y. ; Wang, Chunyan...
European Urology Open Science. 44 (2022) - p. 106-112 , 2022

Link: https://doi.org/10.1016/..

4

Whole exome sequencing identifies potential candidate genes..:

Wang, Chunyan ; Seltzsam, Steve ; Zheng, Bixia...
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1355-1367 , 2022

Link: https://doi.org/10.1002/..

5

Anti-ANGPTL3-FLD monoclonal antibody treatment ameliorates ..:

Lv, Qianying ; Han, Xinli ; Ni, Jiajia...
Cell Death & Disease. 13 (2022) 10 - p. , 2022

Link: https://doi.org/10.1038/..

6

Reverse phenotyping facilitates disease allele calling in e..:

Seltzsam, Steve ; Wang, Chunyan ; Zheng, Bixia...
Genetics in Medicine. 24 (2022) 2 - p. 307-318 , 2022

Link: https://doi.org/10.1016/..

7

RecessiveNOS1APvariants impair actin remodeling and cause g..:

Majmundar, Amar J. ; Buerger, Florian ; Forbes, Thomas A....
Science Advances. 7 (2021) 1 - p. , 2021

Link: https://doi.org/10.1126/..

8

Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as cand..:

Zheng, Bixia ; Seltzsam, Steve ; Wang, Chunyan...
Nephrology Dialysis Transplantation. 37 (2021) 10 - p. 1833-1843 , 2021

Link: https://doi.org/10.1093/..

9

PPARα agonist exerts protective effects in podocyte injury ..:

Han, Xinli ; Lv, Qianying ; Liu, Haimei...
Experimental Cell Research. 407 (2021) 2 - p. 112753 , 2021

Link: https://doi.org/10.1016/..

10

A truncating NRIP1 variant in an Arabic family with congeni..:

Zheng, Bixia ; Wang, Chunyan ; Seltzsam, Steve...
American Journal of Medical Genetics Part A. 188 (2021) 1 - p. 310-313 , 2021

Link: https://doi.org/10.1002/..

11

Exome survey of individuals affected by VATER/VACTERL with ..:

Kolvenbach, Caroline M. ; van der Ven, Amelie T. ; Kause, Franziska...
American Journal of Medical Genetics Part A. 185 (2021) 12 - p. 3784-3792 , 2021

Link: https://doi.org/10.1002/..

12

Phenotype expansion of heterozygous FOXC1 pathogenic varian..:

Wu, Chen-Han Wilfred ; Mann, Nina ; Nakayama, Makiko...
Genetics in Medicine. 22 (2020) 10 - p. 1673-1681 , 2020

Link: https://doi.org/10.1038/..

13

COL4A1 mutations as a potential novel cause of autosomal do..:

Kitzler, Thomas M. ; Schneider, Ronen ; Kohl, Stefan...
Human Genetics. 138 (2019) 10 - p. 1105-1115 , 2019

Link: https://doi.org/10.1007/..

14

Angiopoietin-like-3 knockout protects against glomeruloscle..:

Dai, Rufeng ; Liu, Haimei ; Han, Xinli...
BMC Nephrology. 20 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

15

Anti-proteinuria effect of antibody against ANGPTL3 coil-co..:

Han, Xinli ; Dai, Rufeng ; Zhai, Yihui...
Biochemical and Biophysical Research Communications. 516 (2019) 3 - p. 812-818 , 2019

Link: https://doi.org/10.1016/..