Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Sita Arjune"'
Autor:
Larina A. Karner, Sita Arjune, Polina Todorova, David Maintz, Franziska Grundmann, Thorsten Persigehl, Roman-Ulrich Müller
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 1, p 326 (2022)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic kidney disease. Patients at high risk of severe disease progression should be identified early in order to intervene with supportive and therapeutic measures. However,
Externí odkaz:
https://doaj.org/article/93c2f956b1294d40a624ed2d1de5af8e
Autor:
Anna-Theresa Mellis, Albert L. Misko, Sita Arjune, Ye Liang, Katalin Erdélyi, Tamás Ditrói, Alexander T. Kaczmarek, Peter Nagy, Guenter Schwarz
Publikováno v:
Redox Biology, Vol 38, Iss , Pp 101800- (2021)
Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency are two rare genetic disorders that are caused by impairment of the mitochondrial enzyme sulfite oxidase. Sulfite oxidase is catalyzing the terminal reaction of cellular cysteine
Externí odkaz:
https://doaj.org/article/e85cee264d004d88807490444d134a04
Autor:
Bernhard Schermer, Francesca Fabretti, Maximilian Damagnez, Veronica Di Cristanziano, Eva Heger, Sita Arjune, Nathan A Tanner, Thomas Imhof, Manuel Koch, Alim Ladha, Julia Joung, Jonathan S Gootenberg, Omar O Abudayyeh, Volker Burst, Feng Zhang, Florian Klein, Thomas Benzing, Roman-Ulrich Müller
Publikováno v:
PLoS ONE, Vol 15, Iss 11, p e0238612 (2020)
BackgroundRapid and extensive testing of large parts of the population and specific subgroups is crucial for proper management of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections and decision-making in times of a pandemic outbr
Externí odkaz:
https://doaj.org/article/d5e7d69119164d80be6a22fed0519fa1
Autor:
Borislav Dejanovic, Dennis Lal, Claudia B. Catarino, Sita Arjune, Abdel A. Belaidi, Holger Trucks, Christian Vollmar, Rainer Surges, Wolfram S. Kunz, Susanne Motameny, Janine Altmüller, Anna Köhler, Bernd A. Neubauer, EPICURE Consortium, Peter Nürnberg, Soheyl Noachtar, Günter Schwarz, Thomas Sander
Publikováno v:
Neurobiology of Disease, Vol 67, Iss , Pp 88-96 (2014)
Gephyrin is a postsynaptic scaffolding protein, essential for the clustering of glycine and γ-aminobutyric acid type-A receptors (GABAARs) at inhibitory synapses. An impairment of GABAergic synaptic inhibition represents a key pathway of epileptogen
Externí odkaz:
https://doaj.org/article/0d3c71caf84e4afe864b20bdcfaa14a1
Autor:
Christoph Heinrich Lindemann, Andrea Wenzel, Florian Erger, Lea Middelmann, Julika Borde, Eric Hahnen, Denise Krauß, Simon Oehm, Sita Arjune, Polina Todorova, Kathrin Burgmaier, Max Christoph Liebau, Franziska Grundmann, Bodo B. Beck, Roman-Ulrich Müller
Publikováno v:
Kidney International Reports. 8:455-466
Autor:
Alexander Fuchs, Jennifer Dederichs, Sita Arjune, Polina Todorova, Fabian Wöstmann, Philipp Antczak, Anja Illerhaus, Birgit Gathof, Franziska Grundmann, Roman-Ulrich Müller, Thorsten Annecke
Publikováno v:
Clinical Kidney Journal. 16:384-393
Background Vascular abnormalities and endothelial dysfunction are part of the spectrum of autosomal dominant polycystic kidney disease (ADPKD). The mechanisms behind these manifestations, including potential effects on the endothelial surface layer (
Autor:
Sita Arjune, Franziska Grundmann, Polina Todorova, Claudia Hendrix, Roman Pfister, Henrik ten Freyhaus, Roman-Ulrich Müller
Publikováno v:
Kidney360. 4:150-161
Autor:
Sita Arjune, Simon Oehm, Polina Todorova, Ron T Gansevoort, Stephan J L Bakker, Florian Erger, Thomas Benzing, Volker Burst, Franziska Grundmann, Philipp Antczak, Roman-Ulrich Müller
Publikováno v:
Clinical Kidney Journal.
Background The identification of new biomarkers in autosomal-dominant polycystic kidney disease (ADPKD) is crucial to improve and simplify prognostic assessment as a basis for patient selection for targeted therapies. Post-Hoc-Analyses of the TEMPO 3
Autor:
Polina Todorova, Sita Arjune, Claudia Hendrix, Simon Oehm, Johannes Schmidt, Denise Krauß, Katharina Burkert, Volker Rolf Burst, Thomas Benzing, Volker Boehm, Franziska Grundmann, Roman-Ulrich Müller
Publikováno v:
Kidney International Reports.
Autor:
Julika Pristup, Elke Schaeffeler, Sita Arjune, Ute Hofmann, Jose Angel Santamaria‐Araujo, Patrick Leuthold, Nele Friedrich, Matthias Nauck, Simon Mayr, Mathias Haag, Thomas Muerdter, Franz‐Josef Marner, Mary V. Relling, William E. Evans, Guenter Schwarz, Matthias Schwab
Publikováno v:
Clinical Pharmacology & Therapeutics. 112:808-816
Therapy of molybdenum cofactor (Moco) deficiency has received US Food and Drug Administration (FDA) approval in 2021. Whereas urothione, the urinary excreted catabolite of Moco, is used as diagnostic biomarker for Moco-deficiency, its catabolic pathw