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

STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.

STAG2 缺失会增强 EWS-FLI1 驱动的微卫星增强子活性,从而促进尤文氏肉瘤的侵袭性。

Eyunni Sanjana, Chu Shih-Chun, Guan Mary L, Louw Michaela, Young Eleanor, Carson Sandra E, Gong Jianhui, Cieslik Marcin, Chinnaiyan Arul M, Parolia Abhijit

Reduced STAG2 expression in myelodysplastic neoplasms and acute myeloid leukemia myelodysplasia-related: a potential biomarker associated with aneuploidy and disease progression

骨髓增生异常肿瘤和急性髓系白血病中STAG2表达降低:一种与非整倍体和疾病进展相关的潜在生物标志物

Ferreira da Silva, Beatriz; Carrossini Bastos, Nina; Fonseca Alvarenga, Tatiana; Piergiorge, Rafael Mina; Goulart Moreira, Verônica; Bueno, Ana Paula; Bedran Milito, Cristiane; Santos-Rebouças, Cíntia Barros; De Souza Fernandez, Teresa

Tumor-suppressive activities of SA1/STAG2 and effects of PARP impairment during brain development.

SA1/STAG2 的抑癌活性以及 PARP 功能障碍对大脑发育的影响。

Totaro Simona, Lettieri Antonella, Castiglioni Silvia, Lavezzari Francesco, Gervasini Cristina, Massa Valentina, Vaccari Thomas

Novel variants in STAG2 and PKD1 associate with multiple congenital malformations and autosomal dominant polycystic kidney disease in a Chinese family: A case report and literature review.

中国某家族中 STAG2 和 PKD1 的新变异与多种先天性畸形和常染色体显性多囊肾病相关:病例报告和文献综述。

Yang Qi, Zhang Qiang, Yi Sheng, Zhou Xunzhao, Ruan Yiyan, Zhang Shujie, Yi Shang, Zhang Qinle, Qin Zailng, Luo Jingsi

A CRISPR-Based Humanized Model Reveals Cooperative Role of STAG2 Loss in Familial GATA2-Deficient MDS Progression

基于 CRISPR 的人源化模型揭示了 STAG2 缺失在家族性 GATA2 缺陷型 MDS 进展中的协同作用

Freed, Grace; Quijada-Álamo, Miguel; Lee, Linda; Podar, Nikita; Autar, Subrina; Carcamo, Saul; Fiore, Persephone; Wang, Ke; Martinez, Isabella G; Zhang, Mimi; Saniei, Shayan; Chao, Clifford; Mekerishvili, Levan; Diaz, Zayna; Ma, Sai; Hasson, Dan; Wagenblast, Elvin

Somatic mutations in STAG2 are associated with separated megakaryocyte nuclear lobes in myelodysplastic syndromes

STAG2基因的体细胞突变与骨髓增生异常综合征中巨核细胞核叶分离有关。

Wong, Waihay J; Zon, Rebecca L; Gibson, Christopher J; Ho, Caleb; Pozdnyakova, Olga; Neuberg, Donna; Battinelli, Elisabeth M; Luskin, Marlise R; Tothova, Zuzana; Morgan, Elizabeth A; Ebert, Benjamin L

STAG2-truncating variants reveal a mosaic STAG2 inactivation pattern and compensatory mechanisms involving cohesin complex remodeling.

STAG2 截短变体揭示了 STAG2 的嵌合失活模式和涉及黏连蛋白复合物重塑的补偿机制。

Moronta Gines Macarena, Wessels Marja W, Casa Valentina, van Staveren Thomas, Hof Amber, Chung Wendy K, Willems Marjolaine, Sandestig Anna, Huening Irina, Turnpenny Peter, Lefebvre Mathilde, Parenti Ilaria, Kaiser Frank J, Demmers Jeroen, van Ijcken Wilfred F J, Wendt Kerstin S

Panretinal Congenital Hypertrophy of the RPE in an 8-Year-Old Girl with an X-Linked STAG2 Mutation

一名8岁女孩患有X连锁STAG2基因突变,表现为全视网膜先天性RPE肥大

Kong, Maximilian D; Sylla, Mohamed M; Oh, Jin Kyun; Dedania, Vaidehi S; Soucy, Megan; Demirkol, Aykut; Brodie, Scott E; Maumenee, Irene H; Tsang, Stephen H

A Novel STAG2 Frameshift Variant in Mullegama-Klein-Martinez Syndrome with Complex Conotruncal Heart Defect

伴有复杂圆锥动脉干心脏缺陷的 Mullegama-Klein-Martinez 综合征中发现一种新的 STAG2 移码变异

Wang, Hua

STAG2 regulates polycomb and differentiation in urothelial precursors and bladder cancer

STAG2调控尿路上皮前体细胞和膀胱癌中的多梳蛋白和分化

Park, Youngrok; Xu, Wanying; Yang, Tianyi; Hill, Victoria; He, Xiaoyuan; Sadzewicz, Lisa; Tallon, Luke; Kim, Jung-Sik; Jin, Fulai; Waldman, Todd