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

HMGB2-RAD21 Axis Promotes Fibro/Adipogenic Progenitor Proliferation and Regulates Fat Infiltration.

HMGB2-RAD21轴促进纤维/脂肪生成祖细胞增殖并调节脂肪浸润。

Tong Xian, Liang Ziyun, Duo Tianqi, Pan Liping, Zhu Qi, Liang Jiete, Luo Xianyao, Feng Qingcai, Xu Rong, Liu Yihao, Chen Xu, Chen Luxi, Liu Xiaohong, Chen Yaosheng, Mo Delin

Meiotic cohesin RAD21L shapes 3D genome structure and transcription in the male germline

减数分裂黏连蛋白RAD21L塑造雄性生殖细胞系的三维基因组结构和转录

Marín-Gual, Laia; Vara, Covadonga; Sainz-Urruela, Raquel; Cuartero, Yasmina; Álvarez-González, Lucía; Felipe-Medina, Natalia; Garcia, Francisca; Llano, Elena; Marti-Renom, Marc A; Pendás, Alberto M; Ruiz-Herrera, Aurora

CTCF/RAD21 organize the ground state of chromatin-nuclear speckle association

CTCF/RAD21 调控染色质-核斑点关联的基态

Ruofan Yu ,Shelby Roseman ,Allison P Siegenfeld ,Zachary Gardner ,Son C Nguyen ,Khoa A Tran ,Eric F Joyce ,Rajan Jain ,Brian B Liau ,Ian D Krantz ,Katherine A Alexander ,Shelley L Berger

Mature chromatin packing domains persist after RAD21 depletion in 3D

RAD21 缺失后,成熟的染色质包装域在 3D 中仍然存在

Wing Shun Li, Lucas M Carter, Luay Matthew Almassalha, Ruyi Gong, Emily M Pujadas-Liwag, Tiffany Kuo, Kyle L MacQuarrie, Marcelo Carignano, Cody Dunton, Vinayak Dravid, Masato T Kanemaki, Igal Szleifer, Vadim Backman

Co-Occurrence of RAD21 and TNFAIP3 Mutations in Cornelia de Lange Syndrome with Pustular Psoriasis: Potential Molecular Interactions

科内莉亚·德·兰格综合征合并脓疱型银屑病中 RAD21 和 TNFAIP3 突变的共存:潜在的分子相互作用

Orozco, Beatriz E; Orozco, Cindy V; Meléndez, Esperanza; Mangones, María F; Valderrama, José; Lobato, Adalberto; Garavito-Galofre, Pilar; Vélez, Jorge I; Vidal, Oscar M

Mechanism of METTL14-mediated RAD21 mRNA epigenetic transcriptome modification in inhibiting thyroid cancer development

METTL14介导的RAD21 mRNA表观遗传转录组修饰抑制甲状腺癌发生的机制

Yinzhe Ge,Chen Qin,Mang Xiao

A Cornelia de Lange syndrome NIPBL 5'-UTR mutation reduces cell proliferation in an in vitro model by downregulating RAD21 and β-catenin.

Cornelia de Lange 综合征 NIPBL 5'-UTR 突变通过下调 RAD21 和 β-catenin 来降低体外模型中的细胞增殖。

Chen Qingqing, Chen Yonghua, Zou Chaochun, Wang Chunlin

RAD21L1 Is Sufficient and Effective for Reprogramming Human Sertoli Cells to Phenotypic Spermatogonial Stem Cells Through DNA Methylation and Essential for Male Fertility

RAD21L1 足以且有效地通过 DNA 甲基化将人类睾丸支持细胞重编程为表型精原干细胞,并且对男性生育能力至关重要。

He, Caimei; Cui, Yinghong; Chen, Wei; Li, Chunyun; He, Zuping

RAD21 promotes oncogenesis and lethal progression of prostate cancer

RAD21促进前列腺癌的发生和致命进展

Su, Xiaofeng A; Stopsack, Konrad H; Schmidt, Daniel R; Ma, Duanduan; Li, Zhe; Scheet, Paul A; Penney, Kathryn L; Lotan, Tamara L; Abida, Wassim; DeArment, Elise G; Lu, Kate; Janas, Thomas; Hu, Sofia; Vander Heiden, Matthew G; Loda, Massimo; Boselli, Monica; Amon, Angelika; Mucci, Lorelei A

Author Correction: NIPBL-mediated RAD21 facilitates tumorigenicity by the PI3K pathway in non-small-cell lung cancer

作者更正:NIPBL介导的RAD21通过PI3K通路促进非小细胞肺癌的肿瘤发生

Xu, Xiaoling; Wang, Ding; Xu, Weizhen; Li, Huihui; Chen, Ning; Li, Na; Yao, Qifeng; Chen, Wei; Zhong, Jianxiang; Mao, Weimin