Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Oliver Oliverio"'
Autor:
Guanyi Huang, Anjali Bisaria, Devin L. Wakefield, Tracy M. Yamawaki, Xin Luo, Jingli A. Zhang, Patrick Vigneault, Jinghong Wang, Jeffrey D. Reagan, Oliver Oliverio, Hong Zhou, Chi-Ming Li, Olaia F. Vila, Songli Wang, Fady I. Malik, James J. Hartman, Christopher M. Hale
Publikováno v:
Stem Cell Reports, Vol 18, Iss 1, Pp 220-236 (2023)
Summary: Titin-truncating variants (TTNtv) are the single largest genetic cause of dilated cardiomyopathy (DCM). In this study we modeled disease phenotypes of A-band TTNtv-induced DCM in human induced pluripotent stem cell-derived cardiomyocytes (hi
Externí odkaz:
https://doaj.org/article/30e3b255f0a347979433bbc120f0b28e
Autor:
W. Hans Meisen, Zahra Bahrami Nejad, Miki Hardy, Huiren Zhao, Oliver Oliverio, Songli Wang, Christopher Hale, Michael M. Ollmann, Patrick J. Collins
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 601-611 (2020)
Adeno-associated virus (AAV) has been used extensively as a vector for gene therapy. Despite its widespread use, the mechanisms by which AAV enters the cell and is trafficked to the nucleus are poorly understood. In this study, we performed two poole
Externí odkaz:
https://doaj.org/article/87c619b9cb884418bae6e178de058af5
Publikováno v:
Genome Biology and Evolution
A long-standing mystery of genomic/transcriptomic structure involves spliced leader trans-splicing (SLTS), in which short RNA “tags” transcribed from a distinct genomic locus is added near the 5′ end of RNA transcripts by the spliceosome. SLTS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f100a479746385426cb1bbec32ded11e
https://doi.org/10.1093/gbe/evz217
https://doi.org/10.1093/gbe/evz217
Autor:
Michael T. McMaster, Jason Farrell, Katherine Bianco, Hannah Tilden, Susan J. Fisher, Oliver Oliverio, Yan Zhou, Matthew Gormley
Publikováno v:
Prenatal Diagnosis. 36:812-822
OBJECTIVE Chromosomal aberrations are frequently associated with birth defects and pregnancy losses. Trisomy 13, Trisomy 18 and Trisomy 21 are the most common, clinically relevant fetal aneusomies. This study used a transcriptomics approach to identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::423da256a1326589413d62205e9349c3
https://doi.org/10.1002/pd.4862
https://doi.org/10.1002/pd.4862
Publikováno v:
Inorganica Chimica Acta. 378:115-120
Nickel and cobalt complexes of pyridine-2-carboxaldehyde-2′-pyridylhydrazone (papyH) and N-methyl(pyridine-2-carboxaldehyde-2′-pyridyl-hydrazone) (papyMe) have been fully characterized through electrochemistry, titration, and alkylation with meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::563880e3e4e34da60a1e9bb9464c8f71
https://doi.org/10.1016/j.ica.2011.08.037
https://doi.org/10.1016/j.ica.2011.08.037
Autor:
Katherine Bianco, Matthew Gormley, Jason Farrell, Yan Zhou, Oliver Oliverio, Hannah Tilden, Michael McMaster, Susan J. Fisher
Publikováno v:
Prenatal Diagnosis. 36:i-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abbd95cc047cf212dca0842900bf82ec
https://doi.org/10.1002/pd.4742
https://doi.org/10.1002/pd.4742