E Wolfgang Kuehn
Overview
Explore the profile of E Wolfgang Kuehn including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
39
Citations
1651
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Cosenza-Contreras M, Seredynska A, Vogele D, Pinter N, Brombacher E, Cueto R, et al.
Proteomics
. 2024 Aug;
24(19):e2300491.
PMID: 39126236
State-of-the-art mass spectrometers combined with modern bioinformatics algorithms for peptide-to-spectrum matching (PSM) with robust statistical scoring allow for more variable features (i.e., post-translational modifications) being reliably identified from (tandem-) mass...
2.
Pichler R, Rizzo L, Trondle K, Buhler M, Brucker H, Muller A, et al.
Biomaterials
. 2022 Nov;
291:121910.
PMID: 36403325
Renal tubular cells frequently lose differentiation markers and physiological properties when propagated in conventional cell culture conditions. Embedding cells in 3D microenvironments or controlling their 3D assembly by bioprinting can...
3.
Thuenauer R, Kuhn K, Guo Y, Kotsis F, Xu M, Trefzer A, et al.
mBio
. 2022 May;
13(3):e0081922.
PMID: 35491830
The opportunistic bacterium Pseudomonas aeruginosa can infect mucosal tissues of the human body. To persist at the mucosal barrier, this highly adaptable pathogen has evolved many strategies, including invasion of...
4.
Quatredeniers M, Bienaime F, Ferri G, Isnard P, Poree E, Billot K, et al.
Hum Mol Genet
. 2022 Jan;
31(13):2121-2136.
PMID: 35043953
Renal ciliopathies are the leading cause of inherited kidney failure. In autosomal dominant polycystic kidney disease (ADPKD), mutations in the ciliary gene PKD1 lead to the induction of CCL2, which...
5.
Kotsis F, Janusch H, Li Y, Viau A, Epting D, Kramer-Zucker A, et al.
Biochem Biophys Res Commun
. 2021 Nov;
584:19-25.
PMID: 34753064
The primary cilium is a sensory organelle at the cell surface with integral functions in cell signaling. It contains a microtubular axoneme that is rooted in the basal body (BB)...
6.
Friedrich S, Muller H, Riesterer C, Schuller H, Friedrich K, Worner C, et al.
Sci Rep
. 2021 Jul;
11(1):15139.
PMID: 34301992
Autosomal dominant polycystic kidney disease (ADPKD) affects more than 12 million people worldwide. Mutations in PKD1 and PKD2 cause cyst formation through unknown mechanisms. To unravel the pathogenic mechanisms in...
7.
Peintner L, Venkatraman A, Waeldin A, Hofherr A, Busch T, Voronov A, et al.
Autophagy
. 2020 Sep;
17(9):2384-2400.
PMID: 32967521
Mutations in the gene result in autosomal dominant polycystic kidney disease (ADPKD), the most common monogenetic cause of end-stage renal disease (ESRD) in humans. Previous reports suggested that PKD1, together...
8.
Viau A, Baaziz M, Aka A, Mazloum M, Nguyen C, Kuehn E, et al.
J Am Soc Nephrol
. 2020 Apr;
31(5):1035-1049.
PMID: 32238474
Background: The inactivation of the ciliary proteins polycystin 1 or polycystin 2 leads to autosomal dominant polycystic kidney disease (ADPKD). Although signaling by primary cilia and interstitial inflammation both play...
9.
Viau A, Kotsis F, Boehlke C, Braeg S, Klein M, Nitschke R, et al.
Biochem Biophys Res Commun
. 2019 Nov;
521(2):290-295.
PMID: 31668373
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in PKD1 or PKD2, the genes encoding polycystin 1 (PC1) and polycystin 2 (PC2), respectively. PC1 and PC2 localize to...
10.
Viau A, Bienaime F, Lukas K, Todkar A, Knoll M, Yakulov T, et al.
EMBO J
. 2018 Jun;
37(15).
PMID: 29925518
Polycystic kidney disease (PKD) and other renal ciliopathies are characterized by cysts, inflammation, and fibrosis. Cilia function as signaling centers, but a molecular link to inflammation in the kidney has...