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

The Long and the Short of it: How Cubilin Isoforms are Affected by Genetic Variants

长话短说:立方蛋白亚型如何受基因变异影响

Simons, Matias

Genetic testing in chronic kidney disease of uneXplained cause (CKDx): clinical insights and evolving diagnostic paradigms

不明原因慢性肾脏病(CKDx)的基因检测:临床见解和不断发展的诊断范式

Halbritter, Jan; Simons, Matias

Genetic kidney diseases - from discovery to precision care

遗传性肾脏疾病——从发现到精准治疗

Simons, Matias; Hoefele, Julia

Desaturase-dependent secretory functions of hepatocyte-like cells control systemic lipid metabolism during starvation in Drosophila.

果蝇饥饿期间,肝细胞样细胞的去饱和酶依赖性分泌功能控制着全身脂质代谢。

Li Jiayi, Huang Kerui, Dibra Indira, Liu Ying, Perrimon Norbert, Simons Matias

Arp2/3-dependent regulation of ciliogenesis governs adaptive distal tubular epithelial cell states in kidney disease.

Arp2/3依赖的纤毛发生调控控制着肾脏疾病中远端肾小管上皮细胞的适应性状态。

Rogg Manuel, Weißer Lisa, Maier Jasmin I, Sigle August, Helmstädter Martin, Stigler Marlene, Sammarco Alena, Gräwe Katja, Andreev Grigor, Kark Charlotte, Ramakrishnan Suresh K, Özel Cem, Butt Linus, Arnold Frederic, Bechtel-Walz Wibke, Schilling Oliver, Tanriver Yakup, Brinkkötter Paul, Grabbert Markus, Simons Matias, Werner Martin, Kretz Oliver, Benzing Thomas, Huber Tobias B, Schell Christoph

The interplay between Wnt and mTOR signaling modulates ciliogenesis in human retinal epithelial cells

Wnt和mTOR信号通路之间的相互作用调节人视网膜上皮细胞的纤毛发生

Yuan, Cheng; Neuner, Annett; Streubel, Johanna; Bhanushali, Ayushi; Simons, Matias; Acebrón, Sergio P; Pereira, Gislene

Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERA

不明原因慢性肾脏病(CKDx):欧洲肾脏协会基因与肾脏工作组的共识声明

Halbritter, Jan; Figueres, Lucile; Van Eerde, Albertien M; Capasso, Giovambattista; Hoorn, Ewout J; Nijenhuis, Tom; Perez-Gomez, Maria Vanessa; Sayer, John A; Simons, Matias; Walsh, Stephen; Zagorec, Nikola; Müller, Roman-Ulrich; Cornec-Le Gall, Emilie

10 tips on how to take a proper family history in CKD patient care

慢性肾脏病患者护理中正确采集家族史的10个技巧

Cornec-Le Gall, Emilie; van Eerde, Albertien M; Figueres, Lucile; Simons, Matias; Capasso, Giovambattista; Perez Gomez, Maria Vanessa; Nijenhuis, Tom; Sayer, John A; Zagorec, Nikola; Müller, Roman-Ulrich; Halbritter, Jan

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

人类C端CUBN变异与慢性蛋白尿和正常肾功能相关

Bedin, Mathilda; Boyer, Olivia; Servais, Aude; Li, Yong; Villoing-Gaudé, Laure; Tête, Marie-Josephe; Cambier, Alexandra; Hogan, Julien; Baudouin, Veronique; Krid, Saoussen; Bensman, Albert; Lammens, Florie; Louillet, Ferielle; Ranchin, Bruno; Vigneau, Cecile; Bouteau, Iseline; Isnard-Bagnis, Corinne; Mache, Christoph J; Schäfer, Tobias; Pape, Lars; Gödel, Markus; Huber, Tobias B; Benz, Marcus; Klaus, Günter; Hansen, Matthias; Latta, Kay; Gribouval, Olivier; Morinière, Vincent; Tournant, Carole; Grohmann, Maik; Kuhn, Elisa; Wagner, Timo; Bole-Feysot, Christine; Jabot-Hanin, Fabienne; Nitschké, Patrick; Ahluwalia, Tarunveer S; Köttgen, Anna; Andersen, Christian Brix Folsted; Bergmann, Carsten; Antignac, Corinne; Simons, Matias

Model organisms for functional validation in genetic renal disease

用于遗传性肾脏疾病功能验证的模式生物

Boettcher, Susanne; Simons, Matias