Published Data Registry

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Title ▴AuthorsJournalPublication year
DOI
PMID
Generation of heterozygous (MRli003-A-5) and homozygous (MRli003-A-6) voltage-sensing knock-in human iPSC lines by CRISPR/Cas9 editing of the AAVS1 locus(Open Access) Zhang F, Meier AB, (...), Moretti AStem Cell Research2022
Genetic and modifiable risk factors combine multiplicatively in common disease(Open Access) Pang S, Yengo L, (...), Schunkert HClinical Research in Cardiology2022
Genetically determined intelligence and coronary artery disease risk(Open Access) Li L, Pang S, Zeng L, Güldener U, Schunkert HClinical Research in Cardiology2020
Genetics of coronary artery disease in the post‐GWAS era(Open Access) Chen Z, Schunkert HJournal of Internal Medicine2021
Genome editing for Duchenne muscular dystrophy: a glimpse of the future?(Open Access) Kupatt C, Windisch A, Moretti A, Wolf E, Wurst W, Walter MCGene Therapy2021
HIF1α-AS1 is a DNA:DNA:RNA triplex-forming lncRNA interacting with the HUSH complex(Open Access) Leisegang MS, Bains JK, (...), Brandes RPNature Communications2022
High-throughput optical action potential recordings in hiPSC-derived cardiomyocytes with a genetically encoded voltage indicator in the AAVS1 locus(Open Access) Zhang F, Meier AB, (...), Dorn TFrontiers in Cell and Developmental Biology2022
Human Macrophage Long Intergenic Noncoding RNA, SIMALR, Suppresses Inflammatory Macrophage Apoptosis via NTN1 (Netrin-1)Cynn E, Li DY, (...), Reilly MPArterioscler Thromb Vasc Biol2022
Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy(Open Access) Stenton SL, Sheremet NL, (...), Prokisch HJ Clin Invest2021
Inactivation of Sirt6 ameliorates muscular dystrophy in mdx mice by releasing suppression of utrophin expression(Open Access) Georgieva AM, Guo X, (...), Braun TNature Communications2022