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

Regulation of sodium/calcium homeostasis by BacNa(v) gene therapy rescues cardiac dysfunction in chronic heart failure

通过BacNa(v)基因疗法调节钠/钙稳态可改善慢性心力衰竭患者的心脏功能障碍

Wu, Tianyu; Li, Yongwu; Perelli, Robin M; Siu, Yiu Yan; Tornatore, Anna; Nataren, Josue; Jiang, Xixian; DeLuca, Sophia; Bers, Donald M; Henriquez, Craig; Landstrom, Andrew P; Bursac, Nenad

Crosstalk of NPY and TGFβ orchestrates the signaling to facilitate perineural invasion of oral squamous cell carcinoma.

NPY 和 TGFβ 的相互作用协调信号传导,促进口腔鳞状细胞癌的神经周围侵袭。

Bi Jing, Liu Ketong, Luo Yiru, Zhou Yueqi, Liu Zhengyan, Tao Junting, Wei Jinhui, Landstrom Marene, Mu Yabing, Zang Guangxiang

Early Initiation of Enzyme Replacement Therapy in Infantile Onset Pompe Disease Improves Cardiac Outcomes: A Longitudinal Analysis

早期启动酶替代疗法可改善婴儿期发病庞贝病患者的心脏预后:一项纵向分析

Cohen, Jennifer L; Beaman, M Makenzie; Rodriguez-Rassi, Eleanor; Stafford, V Grace; Smith, P Brian; Landstrom, Andrew P; Kishnani, Priya S

Genetic and Genomic Testing in Cardiovascular Disease: A Policy Statement From the American Heart Association

心血管疾病的基因和基因组检测:美国心脏协会政策声明

Landstrom, Andrew P; Ferguson, Jane F; James, Cynthia A; Key, Kaitlin V; Lanfear, David; Natarajan, Pradeep; Rasmussen-Torvik, Laura J; Reza, Nosheen; Roden, Dan M; Tsao, Philip S; Whitsel, Laurie P; Wung, Shu-Fen

Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel

与肥厚型心肌病相关的基因:ClinGen遗传性心血管疾病基因注释专家组的重新评估

Hespe, Sophie; Waddell, Amber; Asatryan, Babken; Owens, Emma; Thaxton, Courtney; Adduru, Mhy-Lanie; Anderson, Kailyn; Brown, Emily E; Hoffman-Andrews, Lily; Jordan, Elizabeth; Josephs, Katherine; Mayers, Megan; Peters, Stacey; Stafford, Fergus; Bagnall, Richard D; Bronicki, Lucas; Callewaert, Bert; Chahal, C Anwar A; James, Cynthia A; Jarinova, Olga; Landstrom, Andrew P; McNally, Elizabeth M; Murray, Brittney; Muiño-Mosquera, Laura; Parikh, Victoria; Reuter, Chloe; Walsh, Roddy; Wayburn, Bess; Ware, James S; Ingles, Jodie

The Genetic Basis of Sudden Cardiac Death: From Diagnosis to Emerging Genetic Therapies

猝死的遗传基础:从诊断到新兴基因疗法

Dewars, Enya R; Landstrom, Andrew P

A positive allosteric modulator of the β1AR with antagonist activity for catecholaminergic polymorphic ventricular tachycardia

β1AR 的正向变构调节剂,对儿茶酚胺能多形性室性心动过速具有拮抗活性

Alyssa Grogan ,Robin M Perelli ,Seungkirl Ahn ,Haoran Jiang ,Arun Jyothidasan ,Damini Sood ,Chongzhao You ,David I Israel ,Alex Shaginian ,Qiuxia Chen ,Jian Liu ,Jialu Wang ,Jan Steyaert ,Alem W Kahsai ,Andrew P Landstrom ,Robert J Lefkowitz ,Howard A Rockman

Progressive central cardiorespiratory rate downregulation and intensifying epilepsy lead to sudden unexpected death in epilepsy in mouse model of the most common human ATP1A3 mutation

在携带最常见人类ATP1A3突变的小鼠模型中,进行性中枢心肺功能下调和癫痫发作加剧最终导致癫痫猝死。

Hunanyan, Arsen S; Verma, Amitesh; Bidzimou, Minu-Tshyeto; Biswas, Debolina D; Da Cruz, Emily; Srour, Meredith K; Marek, Joshua; Hume, Cordelia; Elmallah, Mai K; Landstrom, Andrew P; Mikati, Mohamad A

Disease penetrance and phenotypic spectrum of desmoplakin variant carriers in the population

人群中桥粒斑蛋白变异携带者的疾病外显率和表型谱

Gurumoorthi, Manasa; Dabbagh, Ghaith Sharaf; Wolfe, Rachel; Hesse, Kerrick; Shah, Ravi; Kurzlechner, Leonie; Yadav, Kanishk; Balint, Brittany; Asatryan, Babken; Sheikh, Farah; Chahal, C Anwar A; Landstrom, Andrew P

Cardiac Troponin C E135A Variant Impairs Myofilament Response to PKA Phosphorylation and Is Associated With Autosomal Dominant Dilated Cardiomyopathy With Diastolic Dysfunction

心肌肌钙蛋白C E135A变异体损害肌丝对PKA磷酸化的反应,并与常染色体显性遗传性扩张型心肌病伴舒张功能障碍相关。

Landim-Vieira, Maicon; Perelli, Robin M; Rodriguez-Garcia, Michelle; Jani, Vivek P; Chastain, Ronnie C; Lamar, Joshua H; Mines, Ellen; Seo, Gwimoon; Araujo Fernandes, Aurelia; Knollmann, Bjorn; Carboni, Michael P; Chelko, Stephen P; Galkin, Vitold E; Chase, P Bryant; Pinto, Jose Renato; Landstrom, Andrew P