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

The FGFR1 N546K mutation confers resistance to pemigatinib in MLN-ZMYM2::FGFR1

FGFR1 N546K 突变赋予 MLN-ZMYM2::FGFR1 对 pemigatinib 的耐药性

Shoumariyeh, Khalid; Haug, Stefan; Schwaab, Juliana; Pfeil, Julie K; Stappenbeck, Jannis; Schmitt-Graeff, Annette; Naumann, Nicole; Waltemode, Greta; Zeiser, Robert; Miething, Cornelius; Hofmann, Wolf-Karsten; Meggendorfer, Manja; Diederichs, Sven; Duyster, Justus; Reiter, Andreas

Neurodevelopmental Disorder and Cortical Myoclonus in ZMYM2 Deficiency

ZMYM2 缺陷引起的神经发育障碍和皮质肌阵挛

Pollini, Luca; Novelli, Maria; Travaglini, Lorena; Panvino, Fabiola; Leuzzi, Vincenzo; Pisani, Francesco; Galosi, Serena

Targeting the ZMYM2-ANXA9 Axis: Organoid Models Illuminate a Novel Pathway to Overcome Oxaliplatin Resistance in Colorectal Cancer

靶向ZMYM2-ANXA9轴:类器官模型揭示克服结直肠癌奥沙利铂耐药性的新途径

Zeng, Shi-Jie; He, Ke; Shi, Zhi

Identifying Drug Combination Strategies for ZMYM2: FGFR1 Fusion Positive Leukemia

确定 ZMYM2:FGFR1 融合阳性白血病的药物联合治疗策略

Huang, Ariane; Beer, Sofia R; Eide, Christopher A; Druker, Brian J; Tyner, Jeffrey W; Leonard, Jessica; Tognon, Cristina E

Myeloid/lymphoid neoplasm with ZMYM2::FGFR1 rearrangement: A complex trilineage phenotypic and clonal evolution with associated genomic alterations

伴有ZMYM2::FGFR1重排的髓系/淋巴系肿瘤:复杂的三系表型和克隆演变以及相关的基因组改变

Chen, Dong; Liu, Guang; Lewis, Michael R; Li, Xia; Ulrickson, Matthew; Nath, Rajneesh; Chen, Weina

DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regions

DNA 序列和染色质修饰因子共同作用,在印迹控制区域赋予表观遗传双稳态

Stefan Butz, Nina Schmolka, Ino D Karemaker, Rodrigo Villaseñor, Isabel Schwarz, Silvia Domcke, Esther C H Uijttewaal, Julian Jude, Florian Lienert, Arnaud R Krebs, Nathalie P de Wagenaar, Xue Bao, Johannes Zuber, Ulrich Elling, Dirk Schübeler, Tuncay Baubec

ZMYM2 restricts 53BP1 at DNA double-strand breaks to favor BRCA1 loading and homologous recombination

ZMYM2 在 DNA 双链断裂处限制 53BP1,以利于 BRCA1 加载和同源重组

Doohyung Lee, Katja Apelt, Seong-Ok Lee, Hsin-Ru Chan, Martijn S Luijsterburg, Justin W C Leung, Kyle M Miller

DUX-miR-344-ZMYM2-Mediated Activation of MERVL LTRs Induces a Totipotent 2C-like State

DUX-miR-344-ZMYM2介导的MERVL LTR激活诱导全能2C样状态

Fan Yang,Xin Huang,Ruge Zang,Jiayu Chen,Miguel Fidalgo,Carlos Sanchez-Priego,Jihong Yang,Alexander Caichen,Fanglin Ma,Todd Macfarlan,Huayan Wang,Shaorong Gao,Hongwei Zhou,Jianlong Wang

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

转录共抑制因子ZMYM2的突变导致综合征性泌尿道畸形

Dervla M Connaughton,Rufeng Dai,Danielle J Owen,Jonathan Marquez,Nina Mann,Adda L Graham-Paquin,Makiko Nakayama,Etienne Coyaud,Estelle M N Laurent,Jonathan R St-Germain,Lot Snijders Blok,Arianna Vino,Verena Klämbt,Konstantin Deutsch,Chen-Han Wilfred Wu,Caroline M Kolvenbach,Franziska Kause,Isabel Ottlewski,Ronen Schneider,Thomas M Kitzler,Amar J Majmundar,Florian Buerger,Ana C Onuchic-Whitford,Mao Youying,Amy Kolb,Daanya Salmanullah,Evan Chen,Amelie T van der Ven,Jia Rao,Hadas Ityel,Steve Seltzsam,Johanna M Rieke,Jing Chen,Asaf Vivante,Daw-Yang Hwang,Stefan Kohl,Gabriel C Dworschak,Tobias Hermle,Mariëlle Alders,Tobias Bartolomaeus,Stuart B Bauer,Michelle A Baum,Eva H Brilstra,Thomas D Challman,Jacob Zyskind,Carrie E Costin , Katrina M Dipple , Floor A Duijkers , Marcia Ferguson , David R Fitzpatrick , Roger Fick , Ian A Glass , Peter J Hulick , Antonie D Kline , Ilona Krey , Selvin Kumar , Weining Lu , Elysa J Marco , Ingrid M Wentzensen,Heather C Mefford , Konrad Platzer,Inna S Povolotskaya , Juliann M Savatt,Natalia V Shcherbakova , Prabha Senguttuvan , Audrey E Squire , Deborah R Stein,Isabelle Thiffault , Victoria Y Voinova , Michael J G Somers,Michael A Ferguson,Avram Z Traum,Ghaleb H Daouk,Ankana Daga,Nancy M Rodig,Paulien A Terhal,Ellen van Binsbergen,Loai A Eid , Velibor Tasic , Hila Milo Rasouly , Tze Y Lim , Dina F Ahram , Ali G Gharavi , Heiko M Reutter , Heidi L Rehm , Daniel G MacArthur , Monkol Lek , Kristen M Laricchia , Richard P Lifton , Hong Xu,Shrikant M Mane , Simone Sanna-Cherchi , Andrew D Sharrocks,Brian Raught,Simon E Fisher , Maxime Bouchard,Mustafa K Khokha,Shirlee Shril,Friedhelm Hildebrandt

The fibronectin type-III (FNIII) domain of ATF7IP contributes to efficient transcriptional silencing mediated by the SETDB1 complex

ATF7IP 的纤连蛋白 III 型 (FNIII) 结构域有助于 SETDB1 复合物介导的有效转录沉默

Takeshi Tsusaka, Kei Fukuda, Chikako Shimura, Masaki Kato, Yoichi Shinkai