Published Data Registry

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Title	Authors ▾	Journal	Publication year	DOI PMID
Monitoring mitochondrial translation in living cells	Yousefi R, Fornasiero EF, (...), Pacheu‐Grau D	EMBO reports	2021	10.15252/embr.202051635 33586863
The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype	Yigit G, Saida K, (...), Altmüller J	Human Mutation	2019	10.1002/humu.23964 31821646
Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state	Yigit G, Sheffer R, (...), Brockmann K	Journal of Medical Genetics	2021	10.1136/jmedgenet-2021-107769 34172529
Cellular models and therapeutic perspectives in hypertrophic cardiomyopathy	Yigit G, Wollnik B	Medizinische Genetik	2021	10.1515/medgen-2021-2094
Stress- and ubiquitylation-dependent phase separation of the proteasome	Yasuda S, Tsuchiya H, (...), Saeki Y	Nature	2020	10.1038/s41586-020-1982-9 32025036
FGFR1 variants contributed to families with tooth agenesis	Yao S, Zhou X, (...), Pan Y	Human Genomics	2023	10.1186/s40246-023-00539-8 37833774
Skeletal Class III Malocclusion Is Associated with ADAMTS2 Variants and Reduced Expression in a Familial Case	Yao S, Zhou X, (...), Pan Y	International Journal of Molecular Sciences	2022	10.3390/ijms231810673 36142585
The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3’-UTR and promoting Rag1 mRNA expression	Xu M, Ito-Kureha T, (...), Heissmeyer V	Nature Communications	2024	10.1038/s41467-024-46371-z 38467629
Non‐negative blind deconvolution for signal processing in a CRISPR‐edited iPSC‐cardiomyocyte model of dilated cardiomyopathy	Xu H, Wali R, (...), Ebert A	FEBS Letters	2021	10.1002/1873-3468.14189 34482543
Oct4 primarily controls enhancer activity rather than accessibility	Xiong L, Tolen EA, (...), Schöler HR	bioRxiv	2021	10.1101/2021.06.28.450119