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

Efficacy of an XPO1 inhibitor in combination with irinotecan in a preclinical colorectal cancer model

XPO1抑制剂联合伊立替康在临床前结直肠癌模型中的疗效

Lentz, Robert W; Dominguez, Adrian T A; Balmaceda, Nicole Baranda; Arcaroli, John J; Bagby, Stacey M; Binns, Cameron A; Smoots, Stephen G; Jackson, Marilyn M; Macbeth, Morgan; Holmstoen, Tessa; Banerjee, Tapahsama; Whitty, Phaedra A; Yi, S Stephen; Lieu, Christopher H; Messersmith, Wells A; Pitts, Todd M

eSIG-Net: Accurate prediction of single-mutation induced perturbations on protein interactions using a language model

eSIG-Net:利用语言模型精确预测单突变对蛋白质相互作用的影响

Pan, Xingxin; Shrawat, Aditya; Raghavan, Sidharth; Dong, Chuanpeng; Yang, Yuntao; Li, Zhao; Zheng, W Jim; Eckhardt, S Gail; Wu, Erxi; Bass, Juan I Fuxman; Jarosz, Daniel F; Chen, Sidi; McGrail, Daniel J; Sheynkman, Gloria M; Huang, Jason H; Sahni, Nidhi; Yi, S Stephen

Disparate leukemia mutations converge on nuclear phase-separated condensates.

不同的白血病突变最终都导致核内相分离凝聚体的形成。

Datar Gandhar K, Khabusheva Elmira, Anand Archish, Beale Joshua, Sadek Marwa, Chen Chun-Wei, Potolitsyna Evdokiia, Alcantara-Contessoto Nayara, Liu Guangyuan, De La Fuente Josephine, Dollinger Christina, Guzman Anna, Martell Alejandra, Wohlan Katharina, Maiti Abhishek, Short Nicholas J, Yi S Stephen, Andresen Vibeke, Gjertsen Bjørn Tore, Falini Brunangelo, Rau Rachel E, Brunetti Lorenzo, Sahni Nidhi, Goodell Margaret A, Riback Joshua A

Rapid iPSC inclusionopathy models shed light on formation, consequence, and molecular subtype of α-synuclein inclusions

快速诱导多能干细胞包涵体病模型揭示了α-突触核蛋白包涵体的形成、后果和分子亚型

Lam, Isabel; Ndayisaba, Alain; Lewis, Amanda J; Fu, YuHong; Sagredo, Giselle T; Kuzkina, Anastasia; Zaccagnini, Ludovica; Celikag, Meral; Sandoe, Jackson; Sanz, Ricardo L; Vahdatshoar, Aazam; Martin, Timothy D; Morshed, Nader; Ichihashi, Toru; Tripathi, Arati; Ramalingam, Nagendran; Oettgen-Suazo, Charlotte; Bartels, Theresa; Boussouf, Manel; Schäbinger, Max; Hallacli, Erinc; Jiang, Xin; Verma, Amrita; Tea, Challana; Wang, Zichen; Hakozaki, Hiroyuki; Yu, Xiao; Hyles, Kelly; Park, Chansaem; Wang, Xinyuan; Theunissen, Thorold W; Wang, Haoyi; Jaenisch, Rudolf; Lindquist, Susan; Stevens, Beth; Stefanova, Nadia; Wenning, Gregor; van de Berg, Wilma D J; Luk, Kelvin C; Sanchez-Pernaute, Rosario; Gómez-Esteban, Juan Carlos; Felsky, Daniel; Kiyota, Yasujiro; Sahni, Nidhi; Yi, S Stephen; Chung, Chee Yeun; Stahlberg, Henning; Ferrer, Isidro; Schöneberg, Johannes; Elledge, Stephen J; Dettmer, Ulf; Halliday, Glenda M; Bartels, Tim; Khurana, Vikram

Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach

先天性心脏侧向性缺陷的基因组罕见变异机制:双基因模型方法

Rai, Archana; Klonowski, Jonathan; Yuan, Bo; Coveler, Karen J; Dardas, Zain; Egab, Iman; Xu, Jiaoyang; Lupo, Philip J; Agopian, A J; Kostka, Dennis; Lo, Cecilia W; Yi, S Stephen; Gelb, Bruce D; Seidman, Christine E; Boerwinkle, Eric; Posey, Jennifer E; Gibbs, Richard A; Lupski, James R; Morris, Shaine A; Coban-Akdemir, Zeynep

Therapeutic potential of PRMT1 as a critical survival dependency target in multiple myeloma

PRMT1作为多发性骨髓瘤中关键生存依赖性靶点的治疗潜力

Hussain, Tabish; Awasthi, Sharad; Shahid, Farid; Yi, S Stephen; Sahni, Nidhi; Aldaz, C Marcelo

Nuclear Phase Separation Drives NPM1-mutant Acute Myeloid Leukemia.

核相分离驱动NPM1突变型急性髓系白血病

Datar Gandhar K, Khabusheva Elmira, Anand Archish, Beale Joshua, Sadek Marwa, Chen Chun-Wei, Potolitsyna Evdokiia, Alcantara-Contessoto Nayara, Liu Guangyuan, De La Fuente Josephine, Dollinger Christina, Guzman Anna, Martell Alejandra, Wohlan Katharina, Maiti Abhishek, Short Nicholas J, Yi S Stephen, Andresen Vibeke, Gjertsen Bjørn Tore, Falini Brunangelo, Rau Rachel E, Brunetti Lorenzo, Sahni Nidhi, Goodell Margaret A, Riback Joshua A

Pervasive mislocalization of pathogenic coding variants underlying human disorders.

人类疾病致病编码变异的普遍错误定位

Lacoste Jessica, Haghighi Marzieh, Haider Shahan, Reno Chloe, Lin Zhen-Yuan, Segal Dmitri, Qian Wesley Wei, Xiong Xueting, Teelucksingh Tanisha, Miglietta Esteban, Shafqat-Abbasi Hamdah, Ryder Pearl V, Senft Rebecca, Cimini Beth A, Murray Ryan R, Nyirakanani Chantal, Hao Tong, McClain Gregory G, Roth Frederick P, Calderwood Michael A, Hill David E, Vidal Marc, Yi S Stephen, Sahni Nidhi, Peng Jian, Gingras Anne-Claude, Singh Shantanu, Carpenter Anne E, Taipale Mikko

Population-level comparisons of gene regulatory networks modeled on high-throughput single-cell transcriptomics data

基于高通量单细胞转录组学数据构建的基因调控网络群体水平比较

Osorio, Daniel; Capasso, Anna; Eckhardt, S Gail; Giri, Uma; Somma, Alexander; Pitts, Todd M; Lieu, Christopher H; Messersmith, Wells A; Bagby, Stacey M; Singh, Harinder; Das, Jishnu; Sahni, Nidhi; Yi, S Stephen; Kuijjer, Marieke L

Uncovering cell-type-specific immunomodulatory variants and molecular phenotypes in COVID-19 using structurally resolved protein networks

利用结构解析的蛋白质网络揭示 COVID-19 中细胞类型特异性免疫调节变异和分子表型

Chhibbar, Prabal; Guha Roy, Priyamvada; Harioudh, Munesh K; McGrail, Daniel J; Yang, Donghui; Singh, Harinder; Hinterleitner, Reinhard; Gong, Yi-Nan; Yi, S Stephen; Sahni, Nidhi; Sarkar, Saumendra N; Das, Jishnu