Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Amy Larson"'
Autor:
Chun Chou, Gregory L. Martin, Gayani Perera, Junya Awata, Amy Larson, Robert Blanton, Michael T. Chin
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/44ff253957e346fb8924810c3dcff37d
Autor:
Chun Chou, Gregory L. Martin, Gayani Perera, Junya Awata, Amy Larson, Robert Blanton, Michael T. Chin
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disorder affecting 1 in 500 people in the general population. Characterized by asymmetric left ventricular hypertrophy, cardiomyocyte disarray and cardiac fibrosis, HCM is
Externí odkaz:
https://doaj.org/article/70a1450d9b0f468c9509965ddb5eba4e
Autor:
Amy Larson, Christina J. Codden, Gordon S. Huggins, Hassan Rastegar, Frederick Y. Chen, Barry J. Maron, Ethan J. Rowin, Martin S. Maron, Michael T. Chin
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Hypertrophic cardiomyopathy (HCM) is considered a primary disorder of the sarcomere resulting in unexplained left ventricular hypertrophy but the paradoxical association of nonmyocyte phenotypes such as fibrosis, mitral valve anomalies and m
Externí odkaz:
https://doaj.org/article/0cc86b8398c3495e9189ce41db16dc30
Autor:
Gayani Perera, Liam Power, Amy Larson, Christina J. Codden, Junya Awata, Rebecca Batorsky, Douglas Strathdee, Michael T. Chin
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 14, p 11594 (2023)
Barth Syndrome, a rare X-linked disorder affecting 1:300,000 live births, results from defects in Tafazzin, an acyltransferase that remodels cardiolipin and is essential for mitochondrial respiration. Barth Syndrome patients develop cardiomyopathy, m
Externí odkaz:
https://doaj.org/article/45bbd6b493924ea09631b72e1a572414
Autor:
Amy Larson, Michael T. Chin
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Single cell sequencing of human heart tissue is technically challenging and methods to cryopreserve heart tissue for obtaining single cell information have not been standardized. Studies published to date have used varying methods
Externí odkaz:
https://doaj.org/article/b840116fb2714bf6b30f11b100e8015f
Autor:
Amy Larson, Towia A. Libermann, Heather Bowditch, Gaurav Das, Nikolaos Diakos, Gordon S. Huggins, Hassan Rastegar, Frederick Y. Chen, Ethan J. Rowin, Martin S. Maron, Michael T. Chin
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2474 (2021)
Left Ventricular Outflow Tract (LVOT) obstruction occurs in approximately 70% of Hypertrophic Cardiomyopathy (HCM) patients and currently requires imaging or invasive testing for diagnosis, sometimes in conjunction with provocative physiological or p
Externí odkaz:
https://doaj.org/article/45a1d431057c4908bdad718d39529696
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 6, Pp 1513-1523 (2016)
Pre-mRNA splicing is an essential component of eukaryotic gene expression and is highly conserved from unicellular yeasts to humans. Here, we present the development and implementation of a sequencing-based reverse genetic screen designed to identify
Externí odkaz:
https://doaj.org/article/8b9f215065b940a9a61700f9a53b56c5
Publikováno v:
The Startup Players Handbook ISBN: 9781484293171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2bc2116317b7a6c72e612ac6d05d854
https://doi.org/10.1007/978-1-4842-9315-7_1
https://doi.org/10.1007/978-1-4842-9315-7_1
Publikováno v:
The Startup Players Handbook ISBN: 9781484293171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c853b92c3d22c504343592281845b9c
https://doi.org/10.1007/978-1-4842-9315-7_6
https://doi.org/10.1007/978-1-4842-9315-7_6
Publikováno v:
The Startup Players Handbook ISBN: 9781484293171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32c54d9114c05336e35960add6667423
https://doi.org/10.1007/978-1-4842-9315-7_16
https://doi.org/10.1007/978-1-4842-9315-7_16