Maack Christoph

Name	Maack Christoph, Univ.-Prof. Dr. med.
Institution	Deutsches Zentrum für Herzinsuffizienz, Universitätsklinikum Würzburg, DE
Address	Am Schwarzenberg 15, Haus A15, 97078
City	Würzburg
State/Province
Country	Germany
Email	Maack_C@ukw.de
Weblink
O2k-Network Lab	DE Wuerzburg Maack C

Labels:

Publications

	Published	Reference
Krause 2023 J Transl Med	2023	Krause J, Nickel A, Madsen A, Aitken-Buck HM, Stoter AMS, Schrapers J, Ojeda F, Geiger K, Kern M, Kohlhaas M, Bertero E, Hofmockel P, Hübner F, Assum I, Heinig M, Müller C, Hansen A, Krause T, Park DD, Just S, Aïssi D, Börnigen D, Lindner D, Friedrich N, Alhussini K, Bening C, Schnabel RB, Karakas M, Iacoviello L, Salomaa V, Linneberg A, Tunstall-Pedoe H, Kuulasmaa K, Kirchhof P, Blankenberg S, Christ T, Eschenhagen T, Lamberts RR, Maack C, Stenzig J, Zeller T (2023) An arrhythmogenic metabolite in atrial fibrillation. https://doi.org/10.1186/s12967-023-04420-z
Kutschka 2023 Basic Res Cardiol	2023	Kutschka I, Bertero E, Wasmus C, Xiao K, Yang L, Chen X, Oshima Y, Fischer M, Erk M, Arslan B, Alhasan L, Grosser D, Ermer KJ, Nickel A, Kohlhaas M, Eberl H, Rebs S, Streckfuss-Bömeke K, Schmitz W, Rehling P, Thum T, Higuchi T, Rabinowitz J, Maack C, Dudek J (2023) Activation of the integrated stress response rewires cardiac metabolism in Barth syndrome. https://doi.org/10.1007/s00395-023-01017-x
Janz 2023 Mol Metab	2023	Janz A, Walz K, Cirnu A, Surjanto J, Urlaub D, Leskien M, Kohlhaas M, Nickel A, Brand T, Nose N, Wörsdörfer P, Wagner N, Higuchi T, Maack C, Dudek J, Lorenz K, Klopocki E, Ergün S, Duff HJ, Gerull B (2023) Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes. https://doi.org/10.1016/j.molmet.2023.101859
Paulus 2022 Basic Res Cardiol	2022	Paulus MG, Renner K, Nickel AG, Brochhausen C, Limm K, Zügner E, Baier MJ, Pabel S, Wallner S, Birner C, Luchner A, Magnes C, Oefner PJ, Stark KJ, Wagner S, Maack C, Maier LS, Streckfuss-Bömeke K, Sossalla S, Dietl A (2022) Tachycardiomyopathy entails a dysfunctional pattern of interrelated mitochondrial functions. https://doi.org/10.1007/s00395-022-00949-0
Donnarumma 2022 Nat Commun	2022	Donnarumma E, Kohlhaas M, Vimont E, Kornobis E, Chaze T, Gianetto QG, Matondo M, Moya-Nilges M, Maack C, Wai T (2022) Mitochondrial Fission Process 1 controls inner membrane integrity and protects against heart failure. https://doi.org/10.1038/s41467-022-34316-3
Betiu 2022 Int J Mol Sci	2022	Bețiu AM, Noveanu L, Hâncu IM, Lascu A, Petrescu L, Maack C, Elmér E, Muntean DM (2022) Mitochondrial effects of common cardiovascular medications: the good, the bad and the mixed. Int J Mol Sci 23:13653. https://doi.org/10.3390/ijms232113653
Bertero 2022 Function (Oxf)	2022	Bertero E, Maack C (2022) Rethinking Mitchell's chemiosmotic theory: potassium dominates over proton flux to drive mitochondrial F1Fo-ATP synthase. Function (Oxf) 3:zqac012. https://doi.org/10.1093/function/zqac012
Ljubojevic-Holzer 2021 Cardiovasc Res	2021	Ljubojevic-Holzer S, Kraler S, Djalinac N, Abdellatif M, Voglhuber J, Schipke J, Schmidt M, Kling KM, Franke GT, Herbst V, Zirlik A, von Lewinski D, Scherr D, Rainer PP, Kohlhaas M, Nickel A, Muehlfeld C, Maack C, Sedej S (2021) Loss of autophagy protein ATG5 impairs cardiac capacity in mice and humans through diminishing mitochondrial abundance and disrupting Ca²⁺ cycling. https://doi.org/10.1093/cvr/cvab112
Bertero 2020 Circ Res	2020	Bertero E, O'Rourke B, Maack C (2020) Mitochondria do not survive calcium overload during transplantation. Circ Res 126:784-86.
Sacchetto 2019 J Clin Med	2019	Sacchetto C, Sequeira V, Bertero E, Dudek J, Maack C, Calore M (2019) Metabolic alterations in inherited cardiomyopathies. J Clin Med 8:2195. https://doi.org/10.3390/jcm8122195
Bertero 2018 Nat Rev Cardiol	2018	Bertero E, Maack C (2018) Metabolic remodelling in heart failure. Nat Rev Cardiol 15:457-70. https://doi.org/10.1038/s41569-018-0044-6

Abstracts

	Published	Reference
Nickel 2018 IOC130	2018	Defects in mitochondrial calcium uptake precede defects of the respiratory chain in X-linked Barth syndrome cardiomyopathy.