Published Data Registry

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Title ▴	Authors	Journal	Publication year	DOI PMID
Artificial peptides to induce membrane denaturation and disruption and modulate membrane composition and fusion	Lāce I, Cotroneo ER, Hesselbarth N, Simeth NA	Journal of Peptide Science	2022	10.1002/psc.3466 36478488
Association of early life stress and cognitive performance in patients with schizophrenia and healthy controls	Senner F, Schneider-Axmann T, (...), Schulze TG	Schizophrenia Research-Cognition	2023	10.1016/j.scog.2023.100280 36846489
Astrocytes control the spiking of mouse visual cortex layer 5 pyramidal neurons	Sundaram SM, Garg P, Leßlich HM, Mathivanan S	Journal of Physiology-London	2021	10.1113/jp281236 33870501
Asymmetric opening of the homopentameric 5-HT3A serotonin receptor in lipid bilayers	Zhang Y, Dijkman PM, (...), Kudryashev M	Nature Communications	2021	10.1038/s41467-021-21016-7 33594077
ATG9 resides on a unique population of small vesicles in presynaptic nerve terminals	Binotti B, Ninov M, (...), Jahn R	Autophagy	2023	10.1080/15548627.2023.2274204 37881948
Atrial fibrillation-associated electrical remodelling in human induced pluripotent stem cell-derived atrial cardiomyocytes: a novel pathway for antiarrhythmic therapy development	Seibertz F, Rubio T, (...), Voigt N	Cardiovascular Research	2023	10.1093/cvr/cvad143 37677054
Author Correction: Deep learning improves macromolecule identification in 3D cellular cryo-electron tomograms	Moebel E, Martinez-Sanchez A, (...), Kervrann C	Nature Methods	2021	10.1038/s41592-021-01349-3 34785810
Author Correction: Selective optogenetic control of Gq signaling using human Neuropsin	Wagdi A, Malan D, (...), Bruegmann T	Nature Communications	2023	10.1038/s41467-022-35612-8 36599836
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene	Pater JA, Penney C, (...), Young T	Human Genetics	2022	10.1007/s00439-022-02444-x 35278131
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta	Moosa S, Yamamoto GL, (...), Netzer C	American Journal of Human Genetics	2019	10.1016/j.ajhg.2019.08.008 31564437