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

Intrinsic muscle stem cell dysfunction underlies functional deficits in models of type 1 diabetes

内在肌肉干细胞功能障碍是1型糖尿病模型中功能缺陷的根本原因。

Chung, Jin D; Trieu, Jennifer; Parker, Benjamin L; Nguyen, John H; Chee, Annabel; Chan, Audrey S; Jayasimhan, Abhirup; Deliyanti, Devy; Houweling, Peter J; Voges, Holly K; Sourris, Karly C; Mills, Richard J; Coughlan, Melinda T; Wilkinson-Berka, Jennifer L; Porrello, Enzo R; Lynch, Gordon S

An FDA-approved drug structurally and phenotypically corrects the K210del mutation in genetic cardiomyopathy models.

FDA 批准的一种药物在结构和表型上纠正了遗传性心肌病模型中的 K210del 突变

Wang Ping, Ahmed Mahmoud Salama, Nguyen Ngoc Uyen Nhi, Menendez-Montes Ivan, Hsu Ching-Cheng, Farag Ayman B, Thet Suwannee, Lam Nicholas T, Wansapura Janaka P, Crossley Eric, Ma Ning, Zhao Shane Rui, Zhang Tiejun, Morimoto Sachio, Singh Rohit, Elhelaly Waleed, Tassin Tara C, Cardoso Alisson C, Williams Noelle S, Pointer Hayley L, Elliott David A, McNamara James W, Watt Kevin I, Porrello Enzo R, Sadayappan Sakthivel, Sadek Hesham A

Automated integration of multi-slice spatial transcriptomics data in 2D and 3D using VR-Omics

利用VR-Omics实现二维和三维多层空间转录组学数据的自动整合

Bienroth, Denis; Charitakis, Natalie; Wong, Dillon; Zhang, Yunhan C; Jaeger-Honz, Sabrina; Ding, Jialin; Watt, Kevin I; Stolper, Julian; Chambers-Smith, Hazel; MacGregor, Duncan; Christiansen, Bronwyn; Vivien, Celine; Piers, Adam T; Waylen, Lisa N; Hoffmann, Lucas B; Tang, Jessica; La, Hue M; Du, Mei R M; Mohenska, Monika; Polo, Jose M; Grimmond, Sean; Scott, Ethan; Rossello, Fernando J; Porrello, Enzo R; Klein, Karsten; Nim, Hieu T; Elliott, David A; Schreiber, Falk; Ramialison, Mirana

Maturation of human cardiac organoids enables complex disease modeling and drug discovery

人类心脏类器官的成熟使得复杂疾病建模和药物发现成为可能。

Pocock, Mark W; Reid, Janice D; Robinson, Harley R; Charitakis, Natalie; Krycer, James R; Foster, Simon R; Fitzsimmons, Rebecca L; Lor, Mary; Devilée, Lynn A C; Batho, Christopher A P; Tuano, Natasha; Howden, Sara E; Vlahos, Katerina; Watt, Kevin I; Piers, Adam T; Bibby, Kaitlyn; McNamara, James W; Sutton, Rebecca; Iaprintsev, Valerii; Mathew, Jacob; Voges, Holly K; Fortuna, Patrick R J; Bass-Stringer, Sebastian; Vivien, Celine; Rae, James; Parton, Robert G; Firulli, Anthony B; Lisowski, Leszek; Huckstep, Hannah; Humphrey, Sean J; Lal, Sean; Konstantinov, Igor E; Weintraub, Robert G; Elliott, David A; Ramialison, Mirana; Porrello, Enzo R; Mills, Richard J; Hudson, James E

Disparities in spatially variable gene calling highlight the need for benchmarking spatial transcriptomics methods

空间变异基因调用结果的差异凸显了对空间转录组学方法进行基准测试的必要性。

Charitakis, Natalie; Salim, Agus; Piers, Adam T; Watt, Kevin I; Porrello, Enzo R; Elliott, David A; Ramialison, Mirana

GLA-modified RNA treatment lowers GB3 levels in iPSC-derived cardiomyocytes from Fabry-affected individuals

GLA修饰的RNA治疗可降低法布里病患者iPSC来源心肌细胞中的GB3水平

Ter Huurne, Menno; Parker, Benjamin L; Liu, Ning Qing; Qian, Elizabeth Ling; Vivien, Celine; Karavendzas, Kathy; Mills, Richard J; Saville, Jennifer T; Abu-Bonsrah, Dad; Wise, Andrea F; Hudson, James E; Talbot, Andrew S; Finn, Patrick F; Martini, Paolo G V; Fuller, Maria; Ricardo, Sharon D; Watt, Kevin I; Nicholls, Kathy M; Porrello, Enzo R; Elliott, David A

Defining the Fetal Gene Program at Single-Cell Resolution in Pediatric Dilated Cardiomyopathy

在儿科扩张型心肌病中以单细胞分辨率定义胎儿基因程序

Mehdiabadi, Neda R; Boon Sim, Choon; Phipson, Belinda; Kalathur, Ravi K R; Sun, Yuliangzi; Vivien, Celine J; Ter Huurne, Menno; Piers, Adam T; Hudson, James E; Oshlack, Alicia; Weintraub, Robert G; Konstantinov, Igor E; Palpant, Nathan J; Elliott, David A; Porrello, Enzo R

propeller: testing for differences in cell type proportions in single cell data

螺旋桨:检测单细胞数据中细胞类型比例的差异

Phipson, Belinda; Sim, Choon Boon; Porrello, Enzo R; Hewitt, Alex W; Powell, Joseph; Oshlack, Alicia

From genome editing to blastocyst complementation: A new horizon in heart transplantation?

从基因组编辑到胚泡互补:心脏移植的新视野?

Konstantinov, Igor E; King, Gregory; Porrello, Enzo R

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy

α蛋白激酶3 (ALPK3) 截短变异体是常染色体显性遗传性肥厚型心肌病的病因之一。

Lopes, Luis R; Garcia-Hernández, Soledad; Lorenzini, Massimiliano; Futema, Marta; Chumakova, Olga; Zateyshchikov, Dmitry; Isidoro-Garcia, Maria; Villacorta, Eduardo; Escobar-Lopez, Luis; Garcia-Pavia, Pablo; Bilbao, Raquel; Dobarro, David; Sandin-Fuentes, Maria; Catalli, Claudio; Gener Querol, Blanca; Mezcua, Ainhoa; Garcia Pinilla, Jose; Bloch Rasmussen, Torsten; Ferreira-Aguar, Ana; Revilla-Martí, Pablo; Basurte Elorz, Maria Teresa; Bautista Paves, Alicia; Ramon Gimeno, Juan; Figueroa, Ana Virginia; Franco-Gutierrez, Raul; Fuentes-Cañamero, Maria Eugenia; Martinez Moreno, Marina; Ortiz-Genga, Martin; Piqueras-Flores, Jesus; Analia Ramos, Karina; Rudzitis, Ainars; Ruiz-Guerrero, Luis; Stein, Ricardo; Triguero-Bocharán, Mayte; de la Higuera, Luis; Ochoa, Juan Pablo; Abu-Bonsrah, Dad; Kwok, Cecilia Y T; Smith, Jacob B; Porrello, Enzo R; Akhtar, Mohammed M; Jager, Joanna; Ashworth, Michael; Syrris, Petros; Elliott, David A; Monserrat, Lorenzo; Elliott, Perry M