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Nucleic Acids Research|September 28, 2021
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiationManuela Lanzafame, Giulia Branca, Claudia Landi, et al.
Stem Cell Research|April 21, 2018
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 geneManuela Mura, Yee-Ki Lee, Monia Ginevrino, et al.
Stem Cells Translational Medicine|November 14, 2020
Human mesenchymal stromal cells do not express ACE2 and TMPRSS2 and are not permissive to SARS-CoV-2 infectionMaria A Avanzini, Manuela Mura, Elena Percivalle, et al.
Cardiovascular Research|May 14, 2026
Machine learning-guided risk stratification for Long QT Syndrome genetic variants with hiPSC-derived cardiomyocytesAleksandr Khudiakov, Manuela Mura, Federica Giannetti, et al.
ACS Nano|July 14, 2011
Homochiral xanthine quintet networks self-assembled on Au(111) surfacesMiao Yu, Jianguo Wang, Manuela Mura, et al.
Stem Cells Translational Medicine|April 1, 2015
Conditioned medium from human amniotic mesenchymal stromal cells limits infarct size and enhances angiogenesisPatrizia Danieli, Giuseppe Malpasso, Maria Chiara Ciuffreda, et al.
Plos Pathogens|November 14, 2007
A paradigm for virus-host coevolution: sequential counter-adaptations between endogenous and exogenous retrovirusesFrederick Arnaud, Marco Caporale, Mariana Varela, et al.
Cardiovascular Research|March 17, 2020
MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genesYee-Ki Lee, Luca Sala, Manuela Mura, et al.
Nucleic Acids Research|January 1, 2016
The RNA-binding protein LARP1 is a post-transcriptional regulator of survival and tumorigenesis in ovarian cancerThomas G Hopkins, Manuela Mura, Hiba A Al-Ashtal, et al.
Cardiovascular Research|February 4, 2017
Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytesMarcella Rocchetti, Luca Sala, Lisa Dreizehnter, et al.
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