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

Prdm9 and meiotic cohesin proteins cooperatively promote DNA double-strand break formation in mammalian spermatocytes

Prdm9 和减数分裂黏连蛋白协同促进哺乳动物精母细胞中 DNA 双链断裂的形成

Bhattacharyya, Tanmoy; Walker, Michael; Powers, Natalie R; Brunton, Catherine; Fine, Alexander D; Petkov, Petko M; Handel, Mary Ann

Differential effects of two catalytic mutations on full-length PRDM9 and its isolated PR/SET domain reveal a case of pseudomodularity.

两种催化突变对全长 PRDM9 及其分离的 PR/SET 结构域的不同影响揭示了假模块性的案例

Powers Natalie R, Billings Timothy, Paigen Kenneth, Petkov Petko M

Tissue-Specific Trans Regulation of the Mouse Epigenome

小鼠表观基因组的组织特异性转录调控

Baker, Christopher L; Walker, Michael; Arat, Seda; Ananda, Guruprasad; Petkova, Pavlina; Powers, Natalie R; Tian, Hui; Spruce, Catrina; Ji, Bo; Rausch, Dylan; Choi, Kwangbom; Petkov, Petko M; Carter, Gregory W; Paigen, Kenneth

Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages

DCDC2 READ1调控元件的全球分布及其与跨语言音素变异的关系

DeMille, Mellissa M C; Tang, Kevin; Mehta, Chintan M; Geissler, Christopher; Malins, Jeffrey G; Powers, Natalie R; Bowen, Beatrice M; Adams, Andrew K; Truong, Dongnhu T; Frijters, Jan C; Gruen, Jeffrey R

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

DCDC2基因中ETV6结合位点的多态性等位基因会增加阅读和语言障碍的风险。

Baple, Emma L; Maroofian, Reza; Chioza, Barry A; Izadi, Maryam; Cross, Harold E; Al-Turki, Saeed; Barwick, Katy; Skrzypiec, Anna; Pawlak, Robert; Wagner, Karin; Coblentz, Roselyn; Zainy, Tala; Patton, Michael A; Mansour, Sahar; Rich, Phillip; Qualmann, Britta; Hurles, Matt E; Kessels, Michael M; Crosby, Andrew H; Tuz, Karina; Bachmann-Gagescu, Ruxandra; O’Day, Diana R; Hua, Kiet; Isabella, Christine R; Phelps, Ian G; Stolarski, Allan E; O’Roak, Brian J; Dempsey, Jennifer C; Lourenco, Charles; Alswaid, Abdulrahman; Bönnemann, Carsten G; Medne, Livija; Nampoothiri, Sheela; Stark, Zornitza; Leventer, Richard J; Topçu, Meral; Cansu, Ali; Jagadeesh, Sujatha; Done, Stephen; Ishak, Gisele E; Glass, Ian A; Shendure, Jay; Neuhauss, Stephan CF; Haldeman-Englert, Chad R; Doherty, Dan; Ferland, Russell J; Garber, Kathryn B; Ratzel, Sarah; Cullinan, Sara B; Powers, Natalie R; Eicher, John D; Butter, Falk; Kong, Yong; Miller, Laura L; Ring, Susan M; Mann, Matthias; Gruen, Jeffrey R

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

染色体 6p22 上的 DYX2 基因座与阅读障碍、语言障碍和智商的关系

Eicher, John D; Powers, Natalie R; Miller, Laura L; Mueller, Kathryn L; Mascheretti, Sara; Marino, Cecilia; Willcutt, Erik G; DeFries, John C; Olson, Richard K; Smith, Shelley D; Pennington, Bruce F; Tomblin, J Bruce; Ring, Susan M; Gruen, Jeffrey R

Genetic influences of resting state fMRI activity in language-related brain regions in healthy controls and schizophrenia patients: a pilot study

健康对照组和精神分裂症患者语言相关脑区静息态功能磁共振成像活动的遗传影响:一项初步研究

Jamadar, Sharna; Powers, Natalie R; Meda, Shashwath A; Calhoun, Vince D; Gelernter, Joel; Gruen, Jeffrey R; Pearlson, Godfrey D