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

Author Correction: Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21

作者更正:HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因

Ranade, Sanjeev S; Li, Feiya; Whalen, Sean; Pelonero, Angelo; Ye, Lin; Huang, Yu; Brand, Abigail; Nishino, Tomohiro; Mital, Rahul; Boileau, Ryan M; Koback, Frances; Padmanabhan, Arun; Yu, Victoria; Cimarosti, Bastien; Presas-Ramos, Diana; Merriman, Alexander F; Wallace, Langley Grace; Nguyen, Annie; Poulis, Nikolaos; Costa, Mauro W; Gifford, Casey A; Pollard, Katherine S; Srivastava, Deepak

Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21.

HMGN1介导的心肌重编程是21三体综合征心脏缺陷的根本原因。

Ranade Sanjeev S, Li Feiya, Whalen Sean, Pelonero Angelo, Ye Lin, Huang Yu, Brand Abigail, Nishino Tomohiro, Mital Rahul, Boileau Ryan M, Koback Frances, Padmanabhan Arun, Yu Victoria, Cimarosti Bastien, Presas-Ramos Diana, Merriman Alexander F, Wallace Langley Grace, Nguyen Annie, Poulis Nikolaos, Costa Mauro W, Gifford Casey A, Pollard Katherine S, Srivastava Deepak

Insights Into Recovery From Acute Fulminant Myocarditis Following Successful Treatment With Ruxolitinib by Comprehensive Single-Cell Profiling

通过全面的单细胞分析深入了解鲁索替尼成功治疗后急性暴发性心肌炎的恢复情况

Qin, Juan; Aras, Mandar A; Song, Evelyn J; Connolly, Andrew J; Zhou, Lylybell; O'Brien, Connor; Salem, Joe-Elie; Padmanabhan, Arun; Moslehi, Javid J

Transcriptomic Profiling of Human Myocardium at Sudden Death to Define Vulnerable Substrate for Lethal Arrhythmias

对猝死者心肌进行转录组分析,以确定致命性心律失常的易感基质

Caudal, Arianne; Liu, Yu; Pang, Paul D; Maison, David P; Nakasuka, Kosuke; Feng, Jean; Schwarzer-Sperber, H S; Schwarzer, Roland; Moffatt, Ellen; Henrich, Timothy J; Padmanabhan, Arun; Connolly, Andrew J; Wu, Joseph C; Tseng, Zian H

Eed controls craniofacial osteoblast differentiation and mesenchymal proliferation from the neural crest.

Eed 控制颅面成骨细胞分化和神经嵴间充质增殖。

Casey-Clyde Tim, Liu S John, Pelonero Angelo, Serrano Juan Antonio Camara, Teng Camilla, Jang Yoon-Gu, Vasudevan Harish N, Padmanabhan Arun, Bush Jeffrey Ohmann, Raleigh David R

Targeting RUNX1 in Macrophages Facilitates Cardiac Recovery

靶向巨噬细胞中的RUNX1可促进心脏恢复

Amrute, Junedh M; Zhu, Ada; Pai, Yun-Ling; Hector-Greene, Melissa; An, Yuqian; Kim, Kenji Rowell; Sheth, Maya U; Padmanabhan, Arun; Lee, Clara Youngna; Yamawaki, Tracy; Sicklinger, Florian; Hartman, Niklas; Bredemeyer, Andrea; Lee, Chang Jie Mick; Xu, Vee; Bell, Lauren; Harmon, Tyler; Shin, Haewon; Parvathaneni, Alekhya; Liu, Lei; Dutta, Amal K; Pruitt, Danielle; Barreda, Jose; Chen, Jing; Shroff, Urvi Nikhil; Nadadur, Rangarajan; Nigro, Jess; Weinheimer, Carla; Kovacs, Atilla; Cui, Jixin; Wang, Chen; Li, Chi-Ming; Kreisel, Daniel; Liu, Yongjian; Foo, Roger S-Y; Schneider, Rebekka K; Engreitz, Jesse M; Mann, Douglas L; Rulifson, Ingrid; Jackson, Simon; Ason, Brandon; Kramann, Rafael; Drakos, Stavros G; Leuschner, Florian; Alexanian, Michael; Lavine, Kory J

ALPK3 heterozygous truncating variants cause late-onset hypertrophic cardiomyopathy with frequent apical involvement and apical aneurysm

ALPK3杂合截断变异体导致迟发性肥厚型心肌病,常伴有心尖受累和心尖动脉瘤。

Busse, Leora; Huth, Emily A; Abraham, Maria Roselle; Abraham, Theodore; Padmanabhan, Arun; Wojciak, Julianne; Wright, Gabrielle; Aatre, Rajani; Campagna, Rachel; Jackson, Erika; Kreykes, Sarah; Lane, Kimberly; Sawyer, Lindsey; Stevens, Chelsea; Thomas, Matthew; VanDyke, Rebecca; Vedantham, Vasanth; Higgs, Emily J

Automated Assessment of Right Atrial Pressure From Ultrasound Videos Using Machine Learning

利用机器学习技术从超声视频中自动评估右心房压力

Yurk, Dominic; Barrios, Joshua P; Labrecque Langlais, Elodie; Avram, Robert; Aras, Mandar A; Abu-Mostafa, Yaser; Padmanabhan, Arun; Tison, Geoffrey H

Single-nucleus RNA/ATAC-seq in early-stage HCM models predicts SWI/SNF-activation in mutant-myocytes, and allele-specific differences in fibroblasts.

早期 HCM 模型中的单核 RNA/ATAC-seq 预测突变肌细胞中的 SWI/SNF 激活,以及成纤维细胞中的等位基因特异性差异

Thottakara Tilo, Padmanabhan Arun, Tanriverdi Talha, Thambidurai Tharika, Diaz-Rg Jose A, Amonkar Sanika R, Olgin Jeffrey E, Long Carlin S, Roselle Abraham M

Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heart.

利用人类胎儿心脏调控图谱,研究先天性心脏缺陷风险变异的分子趋同性

Ma X Rosa, Conley Stephanie D, Kosicki Michael, Bredikhin Danila, Cui Ran, Tran Steven, Sheth Maya U, Qiu Wei-Lin, Chen Sijie, Kundu Soumya, Kang Helen Y, Amgalan Dulguun, Munger Chad J, Duan Lauren, Dang Katherine, Rubio Oriane Matthys, Kany Shinwan, Zamirpour Siavash, DePaolo John, Padmanabhan Arun, Olgin Jeffrey, Damrauer Scott, Andersson Robin, Gu Mingxia, Priest James R, Quertermous Thomas, Qiu Xiaojie, Rabinovitch Marlene, Visel Axel, Pennacchio Len, Kundaje Anshul, Glass Ian A, Gifford Casey A, Pirruccello James P, Goodyer William R, Engreitz Jesse M