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

Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney disease

尿肽特征可将常染色体隐性多囊肾病与其他慢性肾病病因区分开来。

Burgmaier, Kathrin; Buffin-Meyer, Bénédicte; Klein, Julie; Becknell, Brian; McLeod, Daryl; Boeckhaus, Jan; Gross, Oliver; Dafinger, Claudia; Siwy, Justyna; Decramer, Stéphane; Schaefer, Franz; Liebau, Max C; Schanstra, Joost P

TAPT1-at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta

TAPT1——成骨不全症中细胞外基质和信号传导的交汇点

Etich, Julia; Semler, Oliver; Stevenson, Nicola L; Stephan, Alice; Besio, Roberta; Garibaldi, Nadia; Reintjes, Nadine; Dafinger, Claudia; Liebau, Max Christoph; Baumann, Ulrich; Mörgelin, Matthias; Forlino, Antonella; Stephens, David J; Netzer, Christian; Zaucke, Frank; Rehberg, Mirko

Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease

PKHD1/Pkhd1 在人类和小鼠肾脏中对 MYC 表达的差异调节:对隐性多囊肾病的表型影响

Naoe Harafuji #, Chaozhe Yang #, Maoqing Wu, Girija Thiruvengadam, Heather Gordish-Dressman, R Griffin Thompson, P Darwin Bell, Avi Z Rosenberg, Claudia Dafinger, Max C Liebau, Zsuzsanna Bebok, Ljubica Caldovic, Lisa M Guay-Woodford

The effect of mycophenolate mofetil on podocytes in nephrotoxic serum nephritis

霉酚酸酯对肾毒性血清性肾炎足细胞的影响

A Hackl #, E Nüsken #, J Voggel, S E D Abo Zed, J Binz-Lotter, D Unnersjö-Jess, C Müller, G Fink, K Bohl, E Wiesner, P Diefenhardt, C Dafinger, H Chen, M Wohlfarth, R-U Müller, M J Hackl, B Schermer, K-D Nüsken, L T Weber

Primary cilia suppress Ripk3-mediated necroptosis

初级纤毛抑制Ripk3介导的坏死性凋亡

Emilia Kieckhöfer, Gisela G Slaats, Lena K Ebert, Marie-Christine Albert, Claudia Dafinger, Hamid Kashkar, Thomas Benzing, Bernhard Schermer

Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases

原发性 UREC:更好地了解儿童遗传性囊性肾病肾小管上皮病理的来源

Wolfgang H Ziegler, Sarah Lüdiger, Fatima Hassan, Margarita E Georgiadis, Kathrin Swolana, Amrit Khera, Arne Mertens, Doris Franke, Kai Wohlgemuth, Mareike Dahmer-Heath, Jens König, Claudia Dafinger, Max C Liebau, Metin Cetiner, Carsten Bergmann, Birga Soetje, Dieter Haffner

mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy

RRAGD 中的 mTOR 激活突变是导致肾小管病和心肌病的病因

Karl P Schlingmann, François Jouret, Kuang Shen, Anukrati Nigam, Francisco J Arjona, Claudia Dafinger, Pascal Houillier, Deborah P Jones, Felix Kleinerüschkamp, Jun Oh, Nathalie Godefroid, Mehmet Eltan, Tülay Güran, Stéphane Burtey, Marie-Christine Parotte, Jens König, Alina Braun, Caro Bos, Maria I

Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling

影响 Hippo 信号的新突变扩大了 FAT1 肾病的范围

Francesca Fabretti, Nikolai Tschernoster, Florian Erger, Andrea Hedergott, Anja K Buescher, Claudia Dafinger, Bjoern Reusch, Vincent K Köntges, Stefan Kohl, Malte P Bartram, Lutz Thorsten Weber, Holger Thiele, Janine Altmueller, Bernhard Schermer, Bodo B Beck, Sandra Habbig

Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortality

靶向删除 Ruvbl1 会导致表皮发育严重缺陷和围产期死亡

Claudia Dafinger, Thomas Benzing, Jörg Dötsch, Bernhard Schermer, Max C Liebau

The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activation

人类 ARPKD 蛋白纤维囊蛋白的羧基末端可通过调节 SRC 激活来控制 STAT3 信号传导

Claudia Dafinger, Amrei M Mandel, Alina Braun, Heike Göbel, Kathrin Burgmaier, Laura Massella, Antonio Mastrangelo, Jörg Dötsch, Thomas Benzing, Thomas Weimbs, Bernhard Schermer, Max C Liebau