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

9-Phenanthrol inhibits recombinant and arterial myocyte TMEM16A channels

9-菲醇抑制重组和动脉肌细胞TMEM16A通道

Burris, Sarah K; Wang, Qian; Bulley, Simon; Neeb, Zachary P; Jaggar, Jonathan H

TMEM16A/ANO1 channels contribute to the myogenic response in cerebral arteries.

TMEM16A/ANO1 通道有助于脑动脉的肌源性反应

Bulley Simon, Neeb Zachary P, Burris Sarah K, Bannister John P, Thomas-Gatewood Candice M, Jangsangthong Wanchana, Jaggar Jonathan H

Dynamic micro- and macrovascular remodeling in coronary circulation of obese Ossabaw pigs with metabolic syndrome.

肥胖奥萨博猪代谢综合征冠状动脉循环中动态微血管和大血管重塑

Trask Aaron J, Katz Paige S, Kelly Amy P, Galantowicz Maarten L, Cismowski Mary J, West T Aaron, Neeb Zachary P, Berwick Zachary C, Goodwill Adam G, Alloosh Mouhamad, Tune Johnathan D, Sturek Michael, Lucchesi Pamela A

TMEM16A channels generate Ca²⁺-activated Cl⁻ currents in cerebral artery smooth muscle cells

TMEM16A通道在脑动脉平滑肌细胞中产生Ca²⁺激活的Cl⁻电流。

Thomas-Gatewood, Candice; Neeb, Zachary P; Bulley, Simon; Adebiyi, Adebowale; Bannister, John P; Leo, M Dennis; Jaggar, Jonathan H

Contribution of BK(Ca) channels to local metabolic coronary vasodilation: Effects of metabolic syndrome

BK(Ca)通道对局部代谢性冠状动脉舒张的贡献:代谢综合征的影响

Borbouse, Léna; Dick, Gregory M; Payne, Gregory A; Payne, Brittany D; Svendsen, Mark C; Neeb, Zachary P; Alloosh, Mouhamad; Bratz, Ian N; Sturek, Michael; Tune, Johnathan D

Metabolic syndrome reduces the contribution of K+ channels to ischemic coronary vasodilation

代谢综合征会降低钾离子通道对缺血性冠状动脉舒张的贡献

Borbouse, Léna; Dick, Gregory M; Payne, Gregory A; Berwick, Zachary C; Neeb, Zachary P; Alloosh, Mouhamad; Bratz, Ian N; Sturek, Michael; Tune, Johnathan D

Type 1 IP3 receptors activate BKCa channels via local molecular coupling in arterial smooth muscle cells

型 IP3 受体通过动脉平滑肌细胞中的局部分子偶联激活 BKCa 通道。

Zhao, Guiling; Neeb, Zachary P; Leo, M Dennis; Pachuau, Judith; Adebiyi, Adebowale; Ouyang, Kunfu; Chen, Ju; Jaggar, Jonathan H

Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies

LHX4基因中的三个新的错义突变与垂体激素缺乏症的程度不同有关。

Pfaeffle, Roland W; Hunter, Chad S; Savage, Jesse J; Duran-Prado, Mario; Mullen, Rachel D; Neeb, Zachary P; Eiholzer, Urs; Hesse, Volker; Haddad, Nadine G; Stobbe, Heike M; Blum, Werner F; Weigel, Johannes F W; Rhodes, Simon J