日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

STAG1: Bridging the Gap Between Cohesin Complex and Epigenetic Machinery

STAG1:连接黏连蛋白复合物和表观遗传机制的桥梁

Huang, Siqi; Truong, Thy; Wang, Chao; Xie, Xiaofeng; Lin, H-J Lavender; Kelly, Ryan T; Palazzotti, Tiziano; Marchetti, Giulia Bruna; Alfano, Rosa Maria; Bestetti, Ilaria; Finelli, Palma; Milani, Donatella

NIPBL and STAG1 enable loop extrusion by providing differential DNA-cohesin affinity

NIPBL 和 STAG1 通过提供不同的 DNA-黏连蛋白亲和力来促进环挤出。

van Wee, Raman; Asor, Roi; Li, Yiwen; Drechsel, David; Popova, Mariia; Litos, Gabriele; Davidson, Iain F; Peters, Jan-Michael; Kukura, Philipp

STAG1 Disease, Central Precocious Puberty, and Bone Fragility-A Case Report

STAG1 疾病、中枢性性早熟和骨脆性——病例报告

Șerban, Rebecca-Cristiana; Mituț-Velișcu, Andreea-Mădălina; Costache, Andrei; Cima, Luminița-Nicoleta; Niculescu, Carmen; Moroșanu, Aritina; Riza, Anca-Lelia; Streață, Ioana

A novel frameshift STAG1 variant exhibiting haploinsufficiency due to the nonsense-mediated mRNA decay: a case report and literature review

一种新型移码STAG1变异体因无义介导的mRNA降解而表现出单倍体功能不全:病例报告及文献综述

Jiang, Cuicui; Wu, Ke; Zhou, Ying

Neurological Disease Syndrome Caused by a STAG1 Gene Variant: A Case Report and Literature Review

由STAG1基因变异引起的神经系统疾病综合征:病例报告及文献综述

Zhang, Qi; Ren, Ying; Su, Song; Hu, Wandong; Zhang, Hongwei; Zhang, Tong

A Novel De Novo STAG1 Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity

同卵双胞胎神经发育障碍中一种新的STAG1新生变异:临床异质性的新见解

Cipriano, Lorenzo; Russo, Roberta; Andolfo, Immacolata; Manno, Mariangela; Piscopo, Raffaele; Iolascon, Achille; Piscopo, Carmelo

A novel STAG1 variant associated with congenital clubfoot and microphthalmia: A case report

一种与先天性马蹄内翻足和小眼畸形相关的新型STAG1变异:病例报告

Bregvadze, Kakha; Sukhiashvili, Anastasia; Lartsuliani, Megi; Melikidze, Elene; Tkemaladze, Tinatin

Circular RNA circStag1 promotes bone regeneration by interacting with HuR

环状RNA circStag1通过与HuR相互作用促进骨再生

Gaoyang Chen #,Canling Long #,Shang Wang,Zhenmin Wang,Xin Chen,Wanze Tang,Xiaoqin He,Zhiteng Bao,Baoyu Tan,Jin Zhao,Yongheng Xie,Zhizhong Li,Dazhi Yang,Guozhi Xiao,Songlin Peng

Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies

STAG1突变在儿童血液系统恶性肿瘤遗传易感性中的潜在作用

Saitta, Claudia; Rebellato, Stefano; Bettini, Laura Rachele; Giudici, Giovanni; Panini, Nicolò; Erba, Eugenio; Massa, Valentina; Auer, Franziska; Friedrich, Ulrike; Hauer, Julia; Biondi, Andrea; Fazio, Grazia; Cazzaniga, Giovanni

Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome

Cornelia de Lange 综合征中 NIPBL/Scc2 的破坏会引起黏连蛋白全基因组的重新分布,并对转录组产生影响

Patricia Garcia #, Rita Fernandez-Hernandez #, Ana Cuadrado, Ignacio Coca, Antonio Gomez, Maria Maqueda, Ana Latorre-Pellicer, Beatriz Puisac, Feliciano J Ramos, Juan Sandoval, Manel Esteller, Jose Luis Mosquera, Jairo Rodriguez, J Pié, Ana Losada, Ethel Queralt