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

Defining the Protein Phosphatase 2A (PP2A) Subcomplexes That Regulate FoxO Transcription Factor Localization.

确定调控 FoxO 转录因子定位的蛋白磷酸酶 2A (PP2A) 亚复合物

Luperchio Adeline M, Salamango Daniel J

Phenotypic findings associated with variation in elastin

与弹性蛋白变异相关的表型发现

Justice, Anne; Kelly, Melissa A; Bellus, Gary; Green, Joshua D; Zaidi, Raza; Kerrins, Taylor; Josyula, Navya; Luperchio, Teresa R; Kozel, Beth A; Williams, Marc S

Neuron-specific chromatin disruption at CpG islands and aging-related regions in Kabuki syndrome mice

歌舞伎综合征小鼠中 CpG 岛和衰老相关区域的神经元特异性染色质破坏

Boukas, Leandros; Luperchio, Teresa Romeo; Razi, Afrooz; Hansen, Kasper D; Bjornsson, Hans T

Inhibition of ATM-directed antiviral responses by HIV-1 Vif

HIV-1 Vif 对 ATM 介导的抗病毒反应的抑制

Hoi Tong Wong, Adeline M Luperchio, Sean Riley, Daniel J Salamango

Peripheral blood DNA methylation and neuroanatomical responses to HDACi treatment that rescues neurological deficits in a Kabuki syndrome mouse model

外周血 DNA 甲基化和 HDACi 治疗对歌舞伎综合征小鼠模型中神经功能缺损的神经解剖学反应

Sarah Jessica Goodman #, Teresa Romeo Luperchio #, Jacob Ellegood, Eric Chater-Diehl, Jason P Lerch, Hans Tomas Bjornsson, Rosanna Weksberg4

KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans

KMT2D 缺乏会导致小鼠和人类出现神经性听力损失

Allison J Kalinousky, Teresa R Luperchio, Katrina M Schrode, Jacqueline R Harris, Li Zhang, Valerie B DeLeon, Jill A Fahrner, Amanda M Lauer, Hans T Bjornsson

Senescent stroma induces nuclear deformations in cancer cells via the inhibition of RhoA/ROCK/myosin II-based cytoskeletal tension

衰老基质通过抑制 RhoA/ROCK/肌球蛋白 II 的细胞骨架张力诱导癌细胞核变形

Ivie Aifuwa, Byoung Choul Kim, Pratik Kamat, Bartholomew Starich, Anshika Agrawal, Derin Tanrioven, Teresa R Luperchio, Angela M Jimenez Valencia, Tania Perestrelo, Karen Reddy, Taekjip Ha, Jude M Philip

Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation

利用表观遗传机制的孟德尔遗传病来系统地绘制功能性表观遗传变异图谱

Teresa Romeo Luperchio # ,Leandros Boukas # ,Li Zhang ,Genay Pilarowski ,Jenny Jiang ,Allison Kalinousky ,Kasper D Hansen ,Hans T Bjornsson

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

TET3 缺乏会导致人类全血中出现全基因组 DNA 高甲基化表观遗传特征。

Levy, Michael A; Beck, David B; Metcalfe, Kay; Douzgou, Sofia; Sithambaram, Sivagamy; Cottrell, Trudie; Ansar, Muhammad; Kerkhof, Jennifer; Mignot, Cyril; Nougues, Marie-Christine; Keren, Boris; Moore, Hannah W; Oegema, Renske; Giltay, Jacques C; Simon, Marleen; van Jaarsveld, Richard H; Bos, Jessica; van Haelst, Mieke; Motazacker, M Mahdi; Boon, Elles M J; Santen, Gijs W E; Ruivenkamp, Claudia A L; Alders, Marielle; Luperchio, Teresa Romeo; Boukas, Leandros; Ramsey, Keri; Narayanan, Vinodh; Schaefer, G Bradley; Bonasio, Roberto; Doheny, Kimberly F; Stevenson, Roger E; Banka, Siddharth; Sadikovic, Bekim; Fahrner, Jill A

Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

作者更正:TET3 缺乏会导致人类全血中出现全基因组 DNA 高甲基化表观遗传特征。

Levy, Michael A; Beck, David B; Metcalfe, Kay; Douzgou, Sofia; Sithambaram, Sivagamy; Cottrell, Trudie; Ansar, Muhammad; Kerkhof, Jennifer; Mignot, Cyril; Nougues, Marie-Christine; Keren, Boris; Moore, Hannah W; Oegema, Renske; Giltay, Jacques C; Simon, Marleen; van Jaarsveld, Richard H; Bos, Jessica; van Haelst, Mieke; Motazacker, M Mahdi; Boon, Elles M J; Santen, Gijs W E; Ruivenkamp, Claudia A L; Alders, Marielle; Luperchio, Teresa Romeo; Boukas, Leandros; Ramsey, Keri; Narayanan, Vinodh; Schaefer, G Bradley; Bonasio, Roberto; Doheny, Kimberly F; Stevenson, Roger E; Banka, Siddharth; Sadikovic, Bekim; Fahrner, Jill A