Metabolic Epilepsies—Commemorative Issue in Honor of Professor Uwe Heinemann

por Kovács, Richard, Kunz, Wolfram S.
Publicado 2017

cGMP and cAMP differentially regulate differentiation and function of brown adipocytes

por Jennissen, Katja, Haas, Bodo, Kunz, Wolfram S, Pfeifer, Alexander
Publicado 2011

Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging?

por Zsurka, Gábor, Peeva, Viktoriya, Kotlyar, Alexander, Kunz, Wolfram S.
Publicado 2018

Mitochondrial BK Channel Openers CGS7181 and CGS7184 Exhibit Cytotoxic Properties

por Augustynek, Bartłomiej, Koprowski, Piotr, Rotko, Daria, Kunz, Wolfram S., Szewczyk, Adam, Kulawiak, Bogusz
Publicado 2018

Functional Imaging of Mitochondria in Saponin-permeabilized Mice Muscle Fibers

por Kuznetsov, Andrey V., Mayboroda, Oleg, Kunz, Dagmar, Winkler, Kirstin, Schubert, Walter, Kunz, Wolfram S.
Publicado 1998

Mitochondrial Liver Toxicity of Valproic Acid and Its Acid Derivatives Is Related to Inhibition of α-Lipoamide Dehydrogenase

por Kudin, Alexei P., Mawasi, Hafiz, Eisenkraft, Arik, Elger, Christian E., Bialer, Meir, Kunz, Wolfram S.
Publicado 2017

Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans

por Zsurka, Gábor, Kudina, Tatiana, Peeva, Viktoriya, Hallmann, Kerstin, Elger, Christian E, Khrapko, Konstantin, Kunz, Wolfram S
Publicado 2010

Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms

por Konieczny, Patryk, Fuchs, Peter, Reipert, Siegfried, Kunz, Wolfram S., Zeöld, Anikó, Fischer, Irmgard, Paulin, Denise, Schröder, Rolf, Wiche, Gerhard
Publicado 2008

Calcium Ions Regulate K(+) Uptake into Brain Mitochondria: The Evidence for a Novel Potassium Channel

por Skalska, Jolanta, Bednarczyk, Piotr, Piwońska, Marta, Kulawiak, Bogusz, Wilczynski, Grzegorz, Dołowy, Krzysztof, Kudin, Alexei P., Kunz, Wolfram S., Szewczyk, Adam
Publicado 2009

Stilbene derivatives inhibit the activity of the inner mitochondrial membrane chloride channels

por Koszela-Piotrowska, Izabela, Choma, Katarzyna, Bednarczyk, Piotr, Dołowy, Krzysztof, Szewczyk, Adam, Kunz, Wolfram S., Malekova, Lubica, Kominkova, Viera, Ondrias, Karol
Publicado 2007

Replication fork rescue in mammalian mitochondria

por Torregrosa-Muñumer, Rubén, Hangas, Anu, Goffart, Steffi, Blei, Daniel, Zsurka, Gábor, Griffith, Jack, Kunz, Wolfram S., Pohjoismäki, Jaakko L. O.
Publicado 2019

The Fate of Oxidative Strand Breaks in Mitochondrial DNA

por Trombly, Genevieve, Said, Afaf Milad, Kudin, Alexei P., Peeva, Viktoriya, Altmüller, Janine, Becker, Kerstin, Köhrer, Karl, Zsurka, Gábor, Kunz, Wolfram S.
Publicado 2023

Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome

por Hippen, Marius, Zsurka, Gábor, Peeva, Viktoriya, Machts, Judith, Schwiecker, Kati, Debska-Vielhaber, Grazyna, Wiesner, Rudolf J., Vielhaber, Stefan, Kunz, Wolfram S.
Publicado 2021

Primary Skin Fibroblasts as a Model of Parkinson's Disease

por Auburger, Georg, Klinkenberg, Michael, Drost, Jessica, Marcus, Katrin, Morales-Gordo, Blas, Kunz, Wolfram S., Brandt, Ulrich, Broccoli, Vania, Reichmann, Heinz, Gispert, Suzana, Jendrach, Marina
Publicado 2012

Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls

por Reimann, Jens, Lehmann, Diana, Hardy, Steven A., Falkous, Gavin, Knowles, Charlotte V.Y., Jones, Rachel L., Kunz, Wolfram S., Taylor, Robert W., Kornblum, Cornelia
Publicado 2017

Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype

por Zsurka, Gábor, Appel, Maximilian L. T., Nastaly, Maximilian, Hallmann, Kerstin, Hansen, Niels, Nass, Daniel, Baumgartner, Tobias, Surges, Rainer, Hartmann, Gunther, Bartok, Eva, Kunz, Wolfram S.
Publicado 2023

Sustained seizure remission on perampanel in progressive myoclonic epilepsy (Lafora disease)()

por Schorlemmer, Kathrin, Bauer, Sebastian, Belke, Marcus, Hermsen, Anke, Klein, Karl Martin, Reif, Philipp S., Oertel, Wolfgang H., Kunz, Wolfram S., Knake, Susanne, Rosenow, Felix, Strzelczyk, Adam
Publicado 2013

Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits

por von Wrede, Randi, Schidlowski, Martin, Huppertz, Hans-Jürgen, Rüber, Theodor, Ivo, Anja, Baumgartner, Tobias, Hallmann, Kerstin, Zsurka, Gábor, Helmstaedter, Christoph, Surges, Rainer, Kunz, Wolfram S.
Publicado 2022

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases

por von Wrede, Randi, Jeub, Monika, Ariöz, Idil, Elger, Christian E., von Voss, Hubertus, Klein, Hanns-Georg, Becker, Albert J., Schoch, Susanne, Surges, Rainer, Kunz, Wolfram S.
Publicado 2021

Identification of galectin-3 as a novel potential prognostic/predictive biomarker and therapeutic target for cerebral cavernous malformation disease

por Kar, Souvik, Perrelli, Andrea, Bali, Kiran Kumar, Mastrocola, Raffaella, Kar, Arpita, Khan, Bushra, Gand, Luis, Nayak, Arnab, Hartmann, Christian, Kunz, Wolfram S., Samii, Amir, Bertalanffy, Helmut, Retta, Saverio Francesco
Publicado 2023