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

Pioneering new enhancers by GATA3: role of facilitating transcription factors and chromatin remodeling.

GATA3 开创了新的增强子:促进转录因子和染色质重塑的作用

Orlando Krystal A, Grimm Sara A, Wade Paul A

A novel mutant allele of Mta3 in the mouse: genetic analysis of roles in immunity and androgen biology

小鼠Mta3基因的一种新型突变等位基因:免疫和雄激素生物学作用的遗传分析

Chrysovergis, Kaliopi; Headley, Kathryn; Harper, Kathryn M; Moy, Sheryl S; Grimm, Sara A; Jefferson, Wendy N; Sifre, Maria I; Mahapatra, Debabrata; Rodriguez, Yesenia; Williams, Carmen J; Wade, Paul A

Structural and Dynamic Changes of Nucleosome upon GATA3 Binding

GATA3结合后核小体的结构和动态变化

Ishida, Hisashi; Matsumoto, Atsushi; Tanaka, Hiroki; Okuda, Aya; Morishima, Ken; Wade, Paul A; Kurumizaka, Hitoshi; Sugiyama, Masaaki; Kono, Hidetoshi

Multiple tissue-specific epigenetic alterations regulate persistent gene expression changes following developmental DES exposure in mouse reproductive tissues

小鼠生殖组织中,发育期暴露于己烯雌酚后,多种组织特异性表观遗传改变调控着持续存在的基因表达变化。

Jefferson, Tanner B; Wang, Tianyuan; Jefferson, Wendy N; Li, Yin; Hamilton, Katherine J; Wade, Paul A; Williams, Carmen J; Korach, Kenneth S

Beadchip technology to detect DNA methylation in mouse faithfully recapitulates whole-genome bisulfite sequencing

利用Beadchip技术检测小鼠DNA甲基化,能够忠实地重现全基因组亚硫酸氢盐测序的结果。

Martin, Elizabeth M; Grimm, Sara A; Xu, Zongli; Taylor, Jack A; Wade, Paul A

NLRX1 Deficiency Alters the Gut Microbiome and Is Further Exacerbated by Adherence to a Gluten-Free Diet

NLRX1 缺乏会改变肠道菌群,而坚持无麸质饮食会进一步加剧这种改变。

Morrison, Holly A; Liu, Yang; Eden, Kristin; Nagai-Singer, Margaret A; Wade, Paul A; Allen, Irving C

The estrogen receptor/GATA3/FOXA1 transcriptional network: lessons learned from breast cancer

雌激素受体/GATA3/FOXA1转录网络:从乳腺癌中汲取的经验教训

Martin, Elizabeth M; Orlando, Krystal A; Yokobori, Kosuke; Wade, Paul A

Direct readout of heterochromatic H3K9me3 regulates DNMT1-mediated maintenance DNA methylation

异染色质H3K9me3的直接读取调控DNMT1介导的DNA甲基化维持

Ren, Wendan; Fan, Huitao; Grimm, Sara A; Guo, Yiran; Kim, Jae Jin; Yin, Jiekai; Li, Linhui; Petell, Christopher J; Tan, Xiao-Feng; Zhang, Zhi-Min; Coan, John P; Gao, Linfeng; Cai, Ling; Detrick, Brittany; Çetin, Burak; Cui, Qiang; Strahl, Brian D; Gozani, Or; Wang, Yinsheng; Miller, Kyle M; O'Leary, Seán E; Wade, Paul A; Patel, Dinshaw J; Wang, Gang Greg; Song, Jikui

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

CHD4相关综合征:临床表现、基因型-表型相关性及分子基础的全面研究

Weiss, Karin; Lazar, Hayley P; Kurolap, Alina; Martinez, Ariel F; Paperna, Tamar; Cohen, Lior; Smeland, Marie F; Whalen, Sandra; Heide, Solveig; Keren, Boris; Terhal, Pauline; Irving, Melita; Takaku, Motoki; Roberts, John D; Petrovich, Robert M; Schrier Vergano, Samantha A; Kenney, Amy; Hove, Hanne; DeChene, Elizabeth; Quinonez, Shane C; Colin, Estelle; Ziegler, Alban; Rumple, Melissa; Jain, Mahim; Monteil, Danielle; Roeder, Elizabeth R; Nugent, Kimberly; van Haeringen, Arie; Gambello, Michael; Santani, Avni; Medne, Līvija; Krock, Bryan; Skraban, Cara M; Zackai, Elaine H; Dubbs, Holly A; Smol, Thomas; Ghoumid, Jamal; Parker, Michael J; Wright, Michael; Turnpenny, Peter; Clayton-Smith, Jill; Metcalfe, Kay; Kurumizaka, Hitoshi; Gelb, Bruce D; Baris Feldman, Hagit; Campeau, Philippe M; Muenke, Maximilian; Wade, Paul A; Lachlan, Katherine

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

作者更正:CHD3解旋酶结构域突变会导致一种神经发育综合征,伴有巨头畸形和言语语言障碍。

Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H; Nowak, Catherine B; Douglas, Jessica; Swoboda, Kathryn J; Steeves, Marcie A; Sahai, Inderneel; Stumpel, Connie T R M; Stegmann, Alexander P A; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T; Cohen, Ana S A; Agbahovbe, Ruky; Innes, A Micheil; Au, P Y Billie; Rankin, Julia; Anderson, Ilse J; Skinner, Steven A; Louie, Raymond J; Warren, Hannah E; Afenjar, Alexandra; Keren, Boris; Nava, Caroline; Buratti, Julien; Isapof, Arnaud; Rodriguez, Diana; Lewandowski, Raymond; Propst, Jennifer; van Essen, Ton; Choi, Murim; Lee, Sangmoon; Chae, Jong H; Price, Susan; Schnur, Rhonda E; Douglas, Ganka; Wentzensen, Ingrid M; Zweier, Christiane; Reis, André; Bialer, Martin G; Moore, Christine; Koopmans, Marije; Brilstra, Eva H; Monroe, Glen R; van Gassen, Koen L I; van Binsbergen, Ellen; Newbury-Ecob, Ruth; Bownass, Lucy; Bader, Ingrid; Mayr, Johannes A; Wortmann, Saskia B; Jakielski, Kathy J; Strand, Edythe A; Kloth, Katja; Bierhals, Tatjana; Roberts, John D; Petrovich, Robert M; Machida, Shinichi; Kurumizaka, Hitoshi; Lelieveld, Stefan; Pfundt, Rolph; Jansen, Sandra; Deriziotis, Pelagia; Faivre, Laurence; Thevenon, Julien; Assoum, Mirna; Shriberg, Lawrence; Kleefstra, Tjitske; Brunner, Han G; Wade, Paul A; Fisher, Simon E; Campeau, Philippe M