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

CaMKIIδ subtypes differentially regulate infarct formation following ex vivo myocardial ischemia/reperfusion through NF-κB and TNF-α

CaMKIIδ亚型通过NF-κB和TNF-α差异性地调节离体心肌缺血/再灌注后的梗死形成。

Gray, Charles B B; Suetomi, Takeshi; Xiang, Sunny; Mishra, Shikha; Blackwood, Erik A; Glembotski, Christopher C; Miyamoto, Shigeki; Westenbrink, B Daan; Brown, Joan Heller

Selective coupling of the S1P(3) receptor subtype to S1P-mediated RhoA activation and cardioprotection.

选择性地将 S1P(3) 受体亚型与 S1P 介导的 RhoA 激活和心脏保护偶联

Yung Bryan S, Brand Cameron S, Xiang Sunny Y, Gray Charles B B, Means Christopher K, Rosen Hugh, Chun Jerold, Purcell Nicole H, Brown Joan Heller, Miyamoto Shigeki

Mitochondrial reprogramming induced by CaMKIIδ mediates hypertrophy decompensation

CaMKIIδ诱导的线粒体重编程介导肥大失代偿

Westenbrink, B Daan; Ling, Haiyun; Divakaruni, Ajit S; Gray, Charles B B; Zambon, Alexander C; Dalton, Nancy D; Peterson, Kirk L; Gu, Yusu; Matkovich, Scot J; Murphy, Anne N; Miyamoto, Shigeki; Dorn, Gerald W 2nd; Heller Brown, Joan

CaMKIIδ mediates β-adrenergic effects on RyR2 phosphorylation and SR Ca(2+) leak and the pathophysiological response to chronic β-adrenergic stimulation

CaMKIIδ介导β-肾上腺素能受体对RyR2磷酸化和肌浆网Ca²⁺泄漏的影响,以及对慢性β-肾上腺素能刺激的病理生理反应。

Grimm, Michael; Ling, Haiyun; Willeford, Andrew; Pereira, Laetitia; Gray, Charles B B; Erickson, Jeffrey R; Sarma, Satyam; Respress, Jonathan L; Wehrens, Xander H T; Bers, Donald M; Brown, Joan Heller

Ca2+/Calmodulin-dependent protein kinase II δ mediates myocardial ischemia/reperfusion injury through nuclear factor-κB

Ca2+/钙调蛋白依赖性蛋白激酶IIδ通过核因子-κB介导心肌缺血/再灌注损伤

Ling, Haiyun; Gray, Charles B B; Zambon, Alexander C; Grimm, Michael; Gu, Yusu; Dalton, Nancy; Purcell, Nicole H; Peterson, Kirk; Brown, Joan Heller

Location matters: clarifying the concept of nuclear and cytosolic CaMKII subtypes

定位至关重要:阐明核内和胞质CaMKII亚型的概念

Mishra, Shikha; Gray, Charles B B; Miyamoto, Shigeki; Bers, Donald M; Brown, Joan Heller

A functional null mutation of SCN1B in a patient with Dravet syndrome

Dravet综合征患者中发现SCN1B功能性无义突变。

Patino, Gustavo A; Claes, Lieve R F; Lopez-Santiago, Luis F; Slat, Emily A; Dondeti, Raja S R; Chen, Chunling; O'Malley, Heather A; Gray, Charles B B; Miyazaki, Haruko; Nukina, Nobuyuki; Oyama, Fumitaka; De Jonghe, Peter; Isom, Lori L