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

Elucidating the structure and function of the nucleus-The NIH Common Fund 4D Nucleome program

阐明细胞核的结构和功能——美国国立卫生研究院共同基金4D核组计划

Roy, Ananda L; Conroy, Richard S; Taylor, Veronica G; Mietz, Judy; Fingerman, Ian M; Pazin, Michael J; Smith, Phillip; Hutter, Carolyn M; Singer, Dinah S; Wilder, Elizabeth L

EPIGENOMICS OF AGING IN VERTEBRATES

脊椎动物衰老的表观基因组学

Sayers, Eric W; Barrett, Tanya; Benson, Dennis A; Bolton, Evan; Bryant, Stephen H; Canese, Kathi; Chetvernin, Vyacheslav; Church, Deanna M; DiCuccio, Michael; Federhen, Scott; Feolo, Michael; Fingerman, Ian M; Geer, Lewis Y; Helmberg, Wolfgang; Kapustin, Yuri; Landsman, David; Lipman, David J; Lu, Zhiyong; Madden, Thomas L; Madej, Tom; Maglott, Donna R; Marchler-Bauer, Aron; Miller, Vadim; Mizrachi, Ilene; Ostell, James; Panchenko, Anna; Phan, Lon; Pruitt, Kim D; Schuler, Gregory D; Sequeira, Edwin; Sherry, Stephen T; Shumway, Martin; Sirotkin, Karl; Slotta, Douglas; Souvorov, Alexandre; Starchenko, Grigory; Tatusova, Tatiana A; Wagner, Lukas; Wang, Yanli; Wilbur, W John; Yaschenko, Eugene; Ye, Jian; Benayoun, B; Pollina, E A; Brunet, A

NCBI Epigenomics: what's new for 2013

NCBI 表观基因组学:2013 年的新进展

Fingerman, Ian M; Zhang, Xuan; Ratzat, Walter; Husain, Nora; Cohen, Robert F; Schuler, Gregory D

NCBI Epigenomics: a new public resource for exploring epigenomic data sets

NCBI 表观基因组学:一个用于探索表观基因组数据集的全新公共资源

Fingerman, Ian M; McDaniel, Lee; Zhang, Xuan; Ratzat, Walter; Hassan, Tarek; Jiang, Zhifang; Cohen, Robert F; Schuler, Gregory D

Histone H3 K36 methylation is mediated by a trans-histone methylation pathway involving an interaction between Set2 and histone H4

组蛋白H3 K36甲基化是由涉及Set2和组蛋白H4相互作用的跨组蛋白甲基化途径介导的。

Du, Hai-Ning; Fingerman, Ian M; Briggs, Scott D

A charge-based interaction between histone H4 and Dot1 is required for H3K79 methylation and telomere silencing: identification of a new trans-histone pathway.

组蛋白 H4 和 Dot1 之间的电荷相互作用是 H3K79 甲基化和端粒沉默所必需的:一种新的跨组蛋白途径的发现

Fingerman Ian M, Li Hui-Chun, Briggs Scott D

Proteome-wide analysis in Saccharomyces cerevisiae identifies several PHD fingers as novel direct and selective binding modules of histone H3 methylated at either lysine 4 or lysine 36

在酿酒酵母中进行的全蛋白质组分析发现,几个PHD指状结构域是组蛋白H3在赖氨酸4或赖氨酸36位点甲基化的新型直接选择性结合模块。

Shi, Xiaobing; Kachirskaia, Ioulia; Walter, Kay L; Kuo, Jen-Hao A; Lake, Aimee; Davrazou, Foteini; Chan, Steve M; Martin, David G E; Fingerman, Ian M; Briggs, Scott D; Howe, LeAnn; Utz, Paul J; Kutateladze, Tatiana G; Lugovskoy, Alexey A; Bedford, Mark T; Gozani, Or

Global loss of Set1-mediated H3 Lys4 trimethylation is associated with silencing defects in Saccharomyces cerevisiae

酿酒酵母中Set1介导的H3 Lys4三甲基化的整体缺失与基因沉默缺陷相关

Fingerman, Ian M; Wu, Chia-Ling; Wilson, Bradley D; Briggs, Scott D