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

ClC-2 Contributes to Hypotonicity-Induced Adrenal Aldosterone Secretion

ClC-2 促进低渗诱导的肾上腺醛固酮分泌

Volkert, Marina; Dinh, Hoang An; Scholl, Ute I; Stölting, Gabriel

Somatic Mutations in MCOLN3 Are Associated With Aldosterone-Producing Adenomas

MCOLN3基因的体细胞突变与醛固酮瘤相关

van Rooyen, Desmaré; Bandulik, Sascha; Coon, Grace A; Laukemper, Miriam; Kumar-Sinha, Chandan; Udager, Aaron M; Lerario, Antonio M; Lee, Chaelin; Wachtel, Heather; Cohen, Debbie L; Luther, James M; Giordano, Thomas J; Scholl, Ute I; Butz, Frederike; Popp, Bernt; Turcu, Adina F; Warth, Richard; Rainey, William E; Rege, Juilee

Longitudinal Association of Statin Treatment With Insulin Sensitivity and Beta-Cell Function in the PROMISE Cohort

在PROMISE队列研究中,他汀类药物治疗与胰岛素敏感性和β细胞功能的纵向关联

Lai, Kira Zhi Hua; Harris, Stewart B; Retnakaran, Ravi; Hanley, Anthony J G; Schwarz, Ute I

Expression and function of Connexin 43 and Connexin 37 in the murine zona glomerulosa

小鼠肾小球带中连接蛋白 43 和连接蛋白 37 的表达及功能

Gabriel Stölting, Nicole Hellmig, Hoang An Dinh, Frederike Butz, Ali Kerim Secener, Marina Volkert, Ute I Scholl

T- and L-Type Calcium Channels Maintain Calcium Oscillations in the Murine Zona Glomerulosa

T型和L型钙通道维持小鼠肾小球球状带的钙振荡

Dinh, Hoang An; Volkert, Marina; Secener, Ali Kerim; Scholl, Ute I; Stölting, Gabriel

A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and Hypotonia

一种新型新生获得功能性 CACNA1D 变异,可导致先天性震颤、癫痫和肌张力低下等神经发育疾病

Fabian Dannenberg, Arpad Von Moers, Petra Bittigau, Jörn Lange, Sylvia Wiegand, Ferenc Török, Gabriel Stölting, Jörg Striessnig, M Mahdi Motazacker, Marjoleine F Broekema, Markus Schuelke, Angela M Kaindl, Ute I Scholl, Nadine J Ortner

Isradipine therapy in Cacna1dIle772Met/+ mice ameliorates primary aldosteronism and neurologic abnormalities

Cacna1dIle772Met/+ 小鼠接受伊拉地平治疗可改善原发性醛固酮增多症和神经系统异常

Gabriel Stölting, Hoang An Dinh, Marina Volkert, Nicole Hellmig, Julia Schewe, Luise Hennicke, Eric Seidel, Herbert Oberacher, Junhui Zhang, Richard P Lifton, Iris Urban, Melissa Long, Marion Rivalan, Timothy Nottoli, Ute I Scholl

Generation of sheep with defined FecB(B) and TBXT mutations and porcine blastocysts with KCNJ5(G151R/+) mutation using prime editing

利用先导编辑技术生成携带特定 FecB(B) 和 TBXT 突变的绵羊以及携带 KCNJ5(G151R/+) 突变的猪胚泡。

Zhou, Shiwei; Lenk, Laura Johanna; Gao, Yawei; Wang, Yuhui; Zhao, Xiaoe; Pan, Menghao; Huang, Shuhong; Sun, Kexin; Kalds, Peter; Luo, Qi; Lillico, Simon; Sonstegard, Tad; Scholl, Ute I; Ma, Baohua; Petersen, Bjoern; Chen, Yulin; Wang, Xiaolong

DPYD Exon 4 Deletion Associated with Fluoropyrimidine Toxicity and Importance of Copy Number Variation

DPYD 外显子 4 缺失与氟嘧啶毒性相关及拷贝数变异的重要性

Wigle, Theodore J; Medwid, Samantha; Ross, Cameron; Schwarz, Ute I; Kim, Richard B

Genetics of Primary Aldosteronism

原发性醛固酮增多症的遗传学

Scholl, Ute I