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

NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis

NOS1AP 多态性降低 NOS1 活性并与心律失常中的延长复极化相互作用

Carlotta Ronchi, Joyce Bernardi, Manuela Mura, Manuela Stefanello, Beatrice Badone, Marcella Rocchetti, Lia Crotti, Paul Brink, Peter J Schwartz, Massimiliano Gnecchi, Antonio Zaza

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1

从患有常染色体隐性 1 型长 QT 综合征的患者体内生成人类诱导性多能干细胞 (hiPSC) 系 PSMi006-A

Manuela Mura, Francesca Bastaroli, Marzia Corli, Monia Ginevrino, Federica Calabrò, Marina Boni, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Massimiliano Gnecchi

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation

从携带 KCNQ1-R190W 突变的患者体内生成人类诱导性多能干细胞 (hiPSC) 系 PSMi005-A

Manuela Mura, Yee-Ki Lee, Federica Pisano, Monia Ginevrino, Marina Boni, Federica Calabrò, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Hung-Fat Tse, Massimiliano Gnecchi

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation

从 KCNQ1-R594Q 突变携带者中生成人类诱导性多能干细胞 (hiPSC) 系 PSMi004-A

Manuela Mura, Yee-Ki Lee, Federica Pisano, Monia Ginevrino, Marina Boni, Federica Calabrò, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Hung-Fat Tse, Massimiliano Gnecchi

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene

从携带两种常见 NOS1AP 基因变异的 1 型 QT 间期延长综合征患者体内生成人类诱导性多能干细胞 (hiPSC) 系 PSMi007-A

Manuela Mura, Federica Pisano, Manuela Stefanello, Monia Ginevrino, Marina Boni, Federica Calabrò, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Paul A Brink, Massimiliano Gnecchi

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1

从患有常染色体隐性 1 型长 QT 综合征的患者体内生成人类诱导性多能干细胞 (hiPSC) 系 PSMi003-A

Manuela Mura, Monia Ginevrino, Rita Zappatore, Federica Pisano, Marina Boni, Silvia Castelletti, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Massimiliano Gnecchi

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene

从患有杰维尔和兰格-尼尔森综合征且携带 KCNQ1 基因两种复合杂合突变的患者体内生成人类诱导性多能干细胞 (hiPSC) 系 PSMi002-A

Manuela Mura, Yee-Ki Lee, Monia Ginevrino, Rita Zappatore, Federica Pisano, Marina Boni, Federica Dagradi, Lia Crotti, Enza Maria Valente, Peter J Schwartz, Hung-Fat Tse, Massimiliano Gnecchi

The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability

罕见的 Caveolin-3 变体 T78M 的表达会改变心脏离子通道功能和膜兴奋性

Giulia Campostrini, Mattia Bonzanni, Alessio Lissoni, Claudia Bazzini, Raffaella Milanesi, Elena Vezzoli, Maura Francolini, Mirko Baruscotti, Annalisa Bucchi, Ilaria Rivolta, Matteo Fantini, Stefano Severi, Riccardo Cappato, Lia Crotti, Peter J Schwartz, Dario DiFrancesco, Andrea Barbuti

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes

与先天性长 QT 综合征相关的新型钙调蛋白突变影响人类心肌细胞中的钙电流

Daniel C Pipilas, Christopher N Johnson, Gregory Webster, Jurg Schlaepfer, Florence Fellmann, Nicole Sekarski, Lisa M Wren, Kateryna V Ogorodnik, Daniel M Chazin, Walter J Chazin, Lia Crotti, Zahurul A Bhuiyan, Alfred L George Jr

Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanisms

心律失常性钙调蛋白突变通过不同的机制破坏心肌细胞内 Ca2+ 调节

Guo Yin, Faisal Hassan, Ayman R Haroun, Lisa L Murphy, Lia Crotti, Peter J Schwartz, Alfred L George, Jonathan Satin