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

B cells drive neuropathic pain-related behaviors in mice through IgG-Fc gamma receptor signaling

B细胞通过IgG-Fcγ受体信号传导驱动小鼠的神经性疼痛相关行为

Lacagnina, Michael J; Willcox, Kendal F; Boukelmoune, Nabila; Bavencoffe, Alexis; Sankaranarayanan, Ishwarya; Barratt, Daniel T; Zuberi, Younus A; Dayani, Dorsa; Chavez, Melissa V; Lu, Jonathan T; Farinotti, Alex Bersellini; Shiers, Stephanie; Barry, Allison M; Mwirigi, Juliet M; Tavares-Ferreira, Diana; Funk, Geoffrey A; Cervantes, Anna M; Svensson, Camilla I; Walters, Edgar T; Hutchinson, Mark R; Heijnen, Cobi J; Price, Theodore J; Fiore, Nathan T; Grace, Peter M

Stargardt macular dystrophy and therapeutic approaches

Stargardt黄斑营养不良症及其治疗方法

Fujinami, Kaoru; Waheed, Nadia; Laich, Yannik; Yang, Paul; Fujinami-Yokokawa, Yu; Higgins, Joseph J; Lu, Jonathan T; Curtiss, Darin; Clary, Cathryn; Michaelides, Michel

VLDL receptor gene therapy for reducing atherogenic lipoproteins

VLDL受体基因疗法用于减少致动脉粥样硬化脂蛋白

Krauss, Ronald M; Lu, Jonathan T; Higgins, Joseph J; Clary, Cathryn M; Tabibiazar, Ray

Post-Translational Modifications and Diastolic Calcium Leak Associated to the Novel RyR2-D3638A Mutation Lead to CPVT in Patient-Specific hiPSC-Derived Cardiomyocytes

与新型 RyR2-D3638A 突变相关的翻译后修饰和舒张期钙泄漏导致患者特异性 hiPSC 衍生心肌细胞发生儿茶酚胺敏感性室性心动过速 (CPVT)

Acimovic, Ivana; Refaat, Marwan M; Moreau, Adrien; Salykin, Anton; Reiken, Steve; Sleiman, Yvonne; Souidi, Monia; Přibyl, Jan; Kajava, Andrey V; Richard, Sylvain; Lu, Jonathan T; Chevalier, Philippe; Skládal, Petr; Dvořak, Petr; Rotrekl, Vladimir; Marks, Andrew R; Scheinman, Melvin M; Lacampagne, Alain; Meli, Albano C

A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder

导致前层粘蛋白A中ZMPSTE24切割位点消失的突变会引起早衰症。

Wang, Yuexia; Lichter-Konecki, Uta; Anyane-Yeboa, Kwame; Shaw, Jessica E; Lu, Jonathan T; Östlund, Cecilia; Shin, Ji-Yeon; Clark, Lorraine N; Gundersen, Gregg G; Nagy, Peter L; Worman, Howard J

LMNA cardiomyopathy: cell biology and genetics meet clinical medicine

LMNA心肌病:细胞生物学和遗传学与临床医学的交汇

Lu, Jonathan T; Muchir, Antoine; Nagy, Peter L; Worman, Howard J

Slow progressive conduction and contraction defects in loss of Nkx2-5 mice after cardiomyocyte terminal differentiation.

Nkx2-5 缺失小鼠在心肌细胞终末分化后出现缓慢进展的传导和收缩缺陷

Takeda Morihiko, Briggs Laura E, Wakimoto Hiroko, Marks Melissa H, Warren Sonisha A, Lu Jonathan T, Weinberg Ellen O, Robertson Keith D, Chien Kenneth R, Kasahara Hideko

Identification of cardiac-specific myosin light chain kinase

心脏特异性肌球蛋白轻链激酶的鉴定

Chan, Jason Y; Takeda, Morihiko; Briggs, Laura E; Graham, Megan L; Lu, Jonathan T; Horikoshi, Nobuo; Weinberg, Ellen O; Aoki, Hiroki; Sato, Naruki; Chien, Kenneth R; Kasahara, Hideko

Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects

围产期Nkx2-5基因缺失会导致快速传导和收缩缺陷。

Briggs, Laura E; Takeda, Morihiko; Cuadra, Adolfo E; Wakimoto, Hiroko; Marks, Melissa H; Walker, Alexandra J; Seki, Tsugio; Oh, Suk P; Lu, Jonathan T; Sumners, Colin; Raizada, Mohan K; Horikoshi, Nobuo; Weinberg, Ellen O; Yasui, Kenji; Ikeda, Yasuhiro; Chien, Kenneth R; Kasahara, Hideko