Suchergebnisse - "Dai, Rufeng"

PubPharm (35)

1

GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract

enthalten in: Human genomics | 2024

von Du, X. | Wang, C. | Liu, J. | +15

2

GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract

enthalten in: Human genomics | 2024

von Du, X. | Wang, C. | Liu, J. | +15

3

The emerging role of clinical genetics in pediatric patients with chronic kidney disease

enthalten in: Pediatric nephrology (Berlin, Germany) | 2024

von Dai, R. | Wang, C. | Shen, Q. | +1

4

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

enthalten in: Journal of the American Society of Nephrology : JASN | 2023

von Klämbt, V. | Buerger, F. | Wang, C. | +30

5

Angiopoietin-like protein 3 : a novel potential biomarker for nephrotic syndrome in children

enthalten in: Frontiers in pediatrics | 2023

von Wen, F. | Liu, J. | Dai, R. | +9

6

Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney

enthalten in: Nephron | 2023

von Schierbaum, L. | Schneider, S. | Buerger, F. | +12

7

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

enthalten in: European urology open science | 2022

von Wu, C. | Lim, T. | Wang, C. | +33

8

Anti-ANGPTL3-FLD monoclonal antibody treatment ameliorates podocyte lesions through attenuating mitochondrial damage

enthalten in: Cell death & disease | 2022

von Lv, Q. | Han, X. | Ni, J. | +10

9

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

enthalten in: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 2022

von Zheng, B. | Seltzsam, S. | Wang, C. | +14

10

Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models

enthalten in: American journal of medical genetics. Part A | 2022

von Wang, C. | Seltzsam, S. | Zheng, B. | +25