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

GSK3i combinatorial treatments affect CDK4/6 and compensatory pathways in 3D preclinical models of pancreatic neuroendocrine tumors

GSK3i联合疗法影响胰腺神经内分泌肿瘤3D临床前模型中的CDK4/6和补偿通路

Luca, Edlira; Shapiro, Igor; Debaix, Huguette; Zitzmann, Kathrin; Wang, Katharina; Auernhammer, Christoph J; Beuschlein, Felix; Nölting, Svenja; Hantel, Constanze

(Non)canonical Wnt signaling, cytoarchitecture and stemness: new insights from primary nonmetastatic, primary metastatic, regional and distant metastatic models of adrenocortical carcinoma.

(非)经典 Wnt 信号传导、细胞结构和干性:来自肾上腺皮质癌原发性非转移性、原发性转移性、区域性和远处转移性模型的新见解。

Shapiro Igor, Debaix Huguette, Kräuchi Chiara, Abate Andrea, Bornstein Stefan R, Nölting Svenja, Gunz Samuel, Berruti Alfredo, Sigala Sandra, Beuschlein Felix, Luca Edlira, Hantel Constanze

Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness

KCNJ16 缺陷导致一种新型小管病,伴有低钾血症、盐流失、酸碱平衡紊乱和神经性耳聋

Karl P Schlingmann, Aparna Renigunta, Ewout J Hoorn, Anna-Lena Forst, Vijay Renigunta, Velko Atanasov, Sinthura Mahendran, Tahsin Stefan Barakat, Valentine Gillion, Nathalie Godefroid, Alice S Brooks, Dorien Lugtenberg, Jennifer Lake, Huguette Debaix, Christoph Rudin, Bertrand Knebelmann, Stephanie

Author Correction: Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

作者更正:线粒体自噬受损将线粒体疾病与甲基丙二酰辅酶 A 变位酶缺乏症中的上皮应激联系起来

Alessandro Luciani #, Anke Schumann #, Marine Berquez #, Zhiyong Chen #, Daniela Nieri, Mario Failli, Huguette Debaix, Beatrice Paola Festa, Natsuko Tokonami, Andrea Raimondi, Alessio Cremonesi, Diego Carrella, Patrick Forny, Stefan Kölker, Francesca Diomedi Camassei, Francisca Diaz, Carlos T Moraes

Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency

甲基丙二酰辅酶A变位酶缺乏症中,线粒体自噬受损将线粒体疾病与上皮应激联系起来。

Alessandro Luciani #,Anke Schumann #,Marine Berquez #,Zhiyong Chen #,Daniela Nieri,Mario Failli,Huguette Debaix,Beatrice Paola Festa,Natsuko Tokonami,Andrea Raimondi,Alessio Cremonesi,Diego Carrella,Patrick Forny,Stefan Kölker,Francesca Diomedi Camassei,Francisca Diaz,Carlos T Moraes,Diego Di Bernardo,Matthias R Baumgartner,Olivier Devuyst

Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis

Hepsin 介导的尿调节素加工对于盐敏感性和粗上升支稳态至关重要

Eric Olinger, Jennifer Lake, Susan Sheehan, Guglielmo Schiano, Tomoaki Takata, Natsuko Tokonami, Huguette Debaix, Francesco Consolato, Luca Rampoldi, Ron Korstanje, Olivier Devuyst

Impaired autophagy bridges lysosomal storage disease and epithelial dysfunction in the kidney

自噬受损会缓解溶酶体贮积症和肾脏上皮功能障碍

Beatrice Paola Festa, Zhiyong Chen, Marine Berquez, Huguette Debaix, Natsuko Tokonami, Jenny Ann Prange, Glenn van de Hoek, Cremonesi Alessio, Andrea Raimondi, Nathalie Nevo, Rachel H Giles, Olivier Devuyst, Alessandro Luciani

Suppression of microRNA Activity in Kidney Collecting Ducts Induces Partial Loss of Epithelial Phenotype and Renal Fibrosis

抑制肾脏集合管中的 microRNA 活性可导致上皮表型部分丧失和肾脏纤维化

Sachin Hajarnis, Matanel Yheskel, Darren Williams, Thomas Brefort, Bob Glaudemans, Huguette Debaix, Michel Baum, Olivier Devuyst, Vishal Patel

Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes

全基因组荟萃分析揭示镁稳态与代谢表型之间的相互作用

Corre, Tanguy; Arjona, Francisco J; Hayward, Caroline; Youhanna, Sonia; de Baaij, Jeroen H F; Belge, Hendrica; Nägele, Nadine; Debaix, Huguette; Blanchard, Maxime G; Traglia, Michela; Harris, Sarah E; Ulivi, Sheila; Rueedi, Rico; Lamparter, David; Macé, Aurélien; Sala, Cinzia; Lenarduzzi, Stefania; Ponte, Belen; Pruijm, Menno; Ackermann, Daniel; Ehret, Georg; Baptista, Daniela; Polasek, Ozren; Rudan, Igor; Hurd, Toby W; Hastie, Nicholas D; Vitart, Veronique; Waeber, Geràrd; Kutalik, Zoltán; Bergmann, Sven; Vargas-Poussou, Rosa; Konrad, Martin; Gasparini, Paolo; Deary, Ian J; Starr, John M; Toniolo, Daniela; Vollenweider, Peter; Hoenderop, Joost G J; Bindels, René J M; Bochud, Murielle; Devuyst, Olivier

Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression

常见的非编码 UMOD 基因变异通过增加尿调节蛋白的表达来诱发盐敏感性高血压和肾脏损害

Matteo Trudu, Sylvie Janas, Chiara Lanzani, Huguette Debaix, Céline Schaeffer, Masami Ikehata, Lorena Citterio, Sylvie Demaretz, Francesco Trevisani, Giuseppe Ristagno, Bob Glaudemans, Kamel Laghmani, Giacomo Dell'Antonio; SKIPOGH team; Johannes Loffing, Maria P Rastaldi, Paolo Manunta, Olivier Devu