Suchergebnisse - "RFWD3"

PubPharm (29)

1

SMARCAL1 ubiquitylation controls its association with RPA-coated ssDNA and promotes replication fork stability

enthalten in: PLoS biology | 2024

von Yates, M. | Marois, I. | St-Hilaire, E. | +12

2

Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W : Detailed Clinical Report of the Second Case in the Literature

enthalten in: Molecular syndromology | 2023

von Kocagil, S. | Şafak, �. | Saraç, E. | +3

3

Investigation of (Epi)genetic causes in syndromic short children born small for gestational age

enthalten in: European journal of medical genetics | 2023

von Tüysüz, B. | Kasap, B. | Uludağ Alkaya, D. | +7

4

RFWD3 acts as a tumor promotor in the development and progression of bladder cancer

enthalten in: Histology and histopathology | 2023

von Jiang, P. | Xu, Z. | Wu, S. | +3

5

RFWD3 promotes ZRANB3 recruitment to regulate the remodeling of stalled replication forks

enthalten in: The Journal of cell biology | 2023

von Moore, C. | Yalcindag, S. | Czeladko, H. | +8

6

Landscape of pathogenic mutations in premature ovarian insufficiency

enthalten in: Nature medicine | 2023

von Ke, H. | Tang, S. | Guo, T. | +16

CommentIn: Nat Med. 2023 Feb;29(2):315-316. - PMID 36792852

7

RING finger and WD repeat domain 3 regulates proliferation and metastasis through the Wnt/β-catenin signalling pathways in hepatocellular carcinoma

enthalten in: World journal of gastroenterology | 2022

von Liang, R. | Zhang, X. | Zhao, J. | +7

8

Systematic analysis on expression quantitative trait loci identifies a novel regulatory variant in ring finger and WD repeat domain 3 associated with prognosis of pancreatic cancer

enthalten in: Chinese medical journal | 2022

von Zhu, Y. | Peng, X. | Wang, X. | +13

9

Targeted Degradation of 53BP1 Using Ubiquitin Variant Induced Proximity

enthalten in: Biomolecules | 2022

von Aminu, B. | Fux, J. | Mallette, E. | +2

10

A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects

enthalten in: Human mutation | 2021

von George, M. | Solanki, A. | Chavan, N. | +17