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

Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies

致病变异会损害心肌病中的细胞组成和单细胞转录

Reichart, Daniel; Lindberg, Eric L; Maatz, Henrike; Miranda, Antonio M A; Viveiros, Anissa; Shvetsov, Nikolay; Gärtner, Anna; Nadelmann, Emily R; Lee, Michael; Kanemaru, Kazumasa; Ruiz-Orera, Jorge; Strohmenger, Viktoria; DeLaughter, Daniel M; Patone, Giannino; Zhang, Hao; Woehler, Andrew; Lippert, Christoph; Kim, Yuri; Adami, Eleonora; Gorham, Joshua M; Barnett, Sam N; Brown, Kemar; Buchan, Rachel J; Chowdhury, Rasheda A; Constantinou, Chrystalla; Cranley, James; Felkin, Leanne E; Fox, Henrik; Ghauri, Ahla; Gummert, Jan; Kanda, Masatoshi; Li, Ruoyan; Mach, Lukas; McDonough, Barbara; Samari, Sara; Shahriaran, Farnoush; Yapp, Clarence; Stanasiuk, Caroline; Theotokis, Pantazis I; Theis, Fabian J; van den Bogaerdt, Antoon; Wakimoto, Hiroko; Ware, James S; Worth, Catherine L; Barton, Paul J R; Lee, Young-Ae; Teichmann, Sarah A; Milting, Hendrik; Noseda, Michela; Oudit, Gavin Y; Heinig, Matthias; Seidman, Jonathan G; Hubner, Norbert; Seidman, Christine E

Cardiomyocyte BRAF and type 1 RAF inhibitors promote cardiomyocyte and cardiac hypertrophy in mice in vivo

心肌细胞 BRAF 和 1 型 RAF 抑制剂在小鼠体内促进心肌细胞和心脏肥大

Angela Clerk, Daniel N Meijles, Michelle A Hardyman, Stephen J Fuller, Sonia P Chothani, Joshua J Cull, Susanna T E Cooper, Hajed O Alharbi, Konstantinos Vanezis, Leanne E Felkin, Thomais Markou, Samuel J Leonard, Spencer W Shaw, Owen J L Rackham, Stuart A Cook, Peter E Glennon, Mary N Sheppard, Joh

Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy

重新评估单基因扩张型心肌病的遗传贡献

Mazzarotto, Francesco; Tayal, Upasana; Buchan, Rachel J; Midwinter, William; Wilk, Alicja; Whiffin, Nicola; Govind, Risha; Mazaika, Erica; de Marvao, Antonio; Dawes, Timothy J W; Felkin, Leanne E; Ahmad, Mian; Theotokis, Pantazis I; Edwards, Elizabeth; Ing, Alexander Y; Thomson, Kate L; Chan, Laura L H; Sim, David; Baksi, A John; Pantazis, Antonis; Roberts, Angharad M; Watkins, Hugh; Funke, Birgit; O'Regan, Declan P; Olivotto, Iacopo; Barton, Paul J R; Prasad, Sanjay K; Cook, Stuart A; Ware, James S; Walsh, Roddy

Widespread Translational Control of Fibrosis in the Human Heart by RNA-Binding Proteins

RNA结合蛋白对人类心脏纤维化的广泛翻译调控

Chothani, Sonia; Schäfer, Sebastian; Adami, Eleonora; Viswanathan, Sivakumar; Widjaja, Anissa A; Langley, Sarah R; Tan, Jessie; Wang, Mao; Quaife, Nicholas M; Jian Pua, Chee; D'Agostino, Giuseppe; Guna Shekeran, Shamini; George, Benjamin L; Lim, Stella; Yiqun Cao, Elaine; van Heesch, Sebastiaan; Witte, Franziska; Felkin, Leanne E; Christodoulou, Eleni G; Dong, Jinrui; Blachut, Susanne; Patone, Giannino; Barton, Paul J R; Hubner, Norbert; Cook, Stuart A; Rackham, Owen J L

Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling

作者更正:WWP2通过调节SMAD2信号通路来调控病理性心脏纤维化

Chen, Huimei; Moreno-Moral, Aida; Pesce, Francesco; Devapragash, Nithya; Mancini, Massimiliano; Heng, Ee Ling; Rotival, Maxime; Srivastava, Prashant K; Harmston, Nathan; Shkura, Kirill; Rackham, Owen J L; Yu, Wei-Ping; Sun, Xi-Ming; Tee, Nicole Gui Zhen; Tan, Elisabeth Li Sa; Barton, Paul J R; Felkin, Leanne E; Lara-Pezzi, Enrique; Angelini, Gianni; Beltrami, Cristina; Pravenec, Michal; Schafer, Sebastian; Bottolo, Leonardo; Hubner, Norbert; Emanueli, Costanza; Cook, Stuart A; Petretto, Enrico

WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling

WWP2 通过调节 SMAD2 信号传导来调节病理性心脏纤维化

Huimei Chen, Aida Moreno-Moral, Francesco Pesce, Nithya Devapragash, Massimiliano Mancini, Ee Ling Heng, Maxime Rotival, Prashant K Srivastava, Nathan Harmston, Kirill Shkura, Owen J L Rackham, Wei-Ping Yu, Xi-Ming Sun, Nicole Gui Zhen Tee, Elisabeth Li Sa Tan, Paul J R Barton, Leanne E Felkin, Enri

Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy

定量变异分类方法可提高孟德尔遗传病基因检测的产出率和精确度:以肥厚型心肌病为例

Walsh, Roddy; Mazzarotto, Francesco; Whiffin, Nicola; Buchan, Rachel; Midwinter, William; Wilk, Alicja; Li, Nicholas; Felkin, Leanne; Ingold, Nathan; Govind, Risha; Ahmad, Mian; Mazaika, Erica; Allouba, Mona; Zhang, Xiaolei; de Marvao, Antonio; Day, Sharlene M; Ashley, Euan; Colan, Steven D; Michels, Michelle; Pereira, Alexandre C; Jacoby, Daniel; Ho, Carolyn Y; Thomson, Kate L; Watkins, Hugh; Barton, Paul J R; Olivotto, Iacopo; Cook, Stuart A; Ware, James S

A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy

一种以基因为中心的策略,用于识别扩张型心肌病中致病的罕见变异。

Horvat, Claire; Johnson, Renee; Lam, Lien; Munro, Jacob; Mazzarotto, Francesco; Roberts, Angharad M; Herman, Daniel S; Parfenov, Michael; Haghighi, Alireza; McDonough, Barbara; DePalma, Steven R; Keogh, Anne M; Macdonald, Peter S; Hayward, Christopher S; Roberts, Amy; Barton, Paul J R; Felkin, Leanne E; Giannoulatou, Eleni; Cook, Stuart A; Seidman, J G; Seidman, Christine E; Fatkin, Diane

Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes

阐明肥厚型心肌病的遗传结构:重新评估非肌节基因的作用

Walsh, Roddy; Buchan, Rachel; Wilk, Alicja; John, Shibu; Felkin, Leanne E; Thomson, Kate L; Chiaw, Tang Hak; Loong, Calvin Chin Woon; Pua, Chee Jian; Raphael, Claire; Prasad, Sanjay; Barton, Paul J; Funke, Birgit; Watkins, Hugh; Ware, James S; Cook, Stuart A

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

非疾病供体和扩张型心肌病患者心脏转录组的自然遗传变异

Heinig, Matthias; Adriaens, Michiel E; Schafer, Sebastian; van Deutekom, Hanneke W M; Lodder, Elisabeth M; Ware, James S; Schneider, Valentin; Felkin, Leanne E; Creemers, Esther E; Meder, Benjamin; Katus, Hugo A; Rühle, Frank; Stoll, Monika; Cambien, François; Villard, Eric; Charron, Philippe; Varro, Andras; Bishopric, Nanette H; George, Alfred L Jr; Dos Remedios, Cristobal; Moreno-Moral, Aida; Pesce, Francesco; Bauerfeind, Anja; Rüschendorf, Franz; Rintisch, Carola; Petretto, Enrico; Barton, Paul J; Cook, Stuart A; Pinto, Yigal M; Bezzina, Connie R; Hubner, Norbert