Published Data Registry

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Title ▴AuthorsJournalPublication year
DOI
PMID
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.(Open Access) Ehmke N, Graul-Neumann L, (...), Kornak UAmerican journal of human genetics2017
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentGordon CT, Xue S, (...), Reversade BNature Genetics2017
Deconstructing sarcomeric structure–function relations in titin-BioID knock-in mice(Open Access) Rudolph F, Fink C, (...), Gotthardt MNature Communications2020
Deep phenotyping of human induced pluripotent stem cell–derived atrial and ventricular cardiomyocytes(Open Access) Cyganek L, Tiburcy M, (...), Guan KJCI Insight2018
Defective COX1 expression in aging mice liver(Open Access) Witte S, Boshnakovska A, Özdemir M, Chowdhury A, Rehling P, Aich ABiology Open2023
Defective Mitochondrial Cardiolipin Remodeling Dampens HIF-1α Expression in Hypoxia(Open Access) Chowdhury A, Aich A, (...), Dudek JCell Reports2018
Defective mitochondrial COX1 translation due to loss of COX14 function triggers ROS-induced inflammation in mouse liver(Open Access) Aich A, Boshnakovska A, (...), Rehling PNature Communications2024
Defined Engineered Human Myocardium for Disease Modeling, Drug Screening, and Heart RepairTiburcy M, Meyer T, Satin P, Zimmermann WMethods in Molecular Biology2022
Defined Engineered Human Myocardium with Advanced Maturation for Applications in Heart Failure Modelling and Repair.(Open Access) Tiburcy M, Hudson JE, (...), Zimmermann WHCirculation2017
Deranged myofilament phosphorylation and function in experimental heart failure with preserved ejection fraction(Open Access) Hamdani N, Bishu KG, von Frieling-Salewsky M, Redfield MM, Linke WA,Cardiovascular Research2013