Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Shelley D Miyamoto"'
Autor:
Frehiwet T. Hailu, Anis Karimpour-Fard, Bonnie Neltner, Brian L. Stauffer, Steven Lipshultz, Shelley D. Miyamoto, Carmen C. Sucharov
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 10, Iss 9, p 391 (2023)
microRNAs (miRs) are small non-coding single-stranded RNAs that regulate gene expression. We previously evaluated expression of miRs in the cardiac tissue of children with dilated cardiomyopathy (DCM) using miRNA-seq. However, a comparative analysis
Externí odkaz:
https://doaj.org/article/cd2d614129954abcb7489f5e74a5469d
Autor:
Danielle A. Jeffrey, Julie Pires Da Silva, Anastacia M. Garcia, Xuan Jiang, Anis Karimpour-Fard, Lee S. Toni, Thomas Lanzicher, Brisa Peña, Carissa A. Miyano, Karin Nunley, Armin Korst, Orfeo Sbaizero, Matthew R.G. Taylor, Shelley D. Miyamoto, Brian L. Stauffer, Carmen C. Sucharov
Publikováno v:
JCI Insight, Vol 6, Iss 19 (2021)
Dilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and main indication for heart transplantation in children. Therapies specific to pediatric DCM remain limited due to lack of a disease model. Our previous study showed that treatm
Externí odkaz:
https://doaj.org/article/b56694d569914cfb80039696f950b52d
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 5, p 152 (2022)
Significant surgical and medical advances over the past several decades have resulted in a growing number of infants and children surviving with hypoplastic left heart syndrome (HLHS) and other congenital heart defects associated with a single system
Externí odkaz:
https://doaj.org/article/48a35e960bb54a1e83b4bc200a8fae38
Autor:
Alexander R. Opotowsky, Kiona Y. Allen, Emily M. Bucholz, Kristin M. Burns, Pedro del Nido, Kathleen N. Fenton, Bruce D. Gelb, James N. Kirkpatrick, Shelby Kutty, Linda M. Lambert, Keila N. Lopez, Laura J. Olivieri, Nathan M. Pajor, Sara K. Pasquali, Christopher J. Petit, Erica Sood, John M. VanBuren, Gail D. Pearson, Shelley D. Miyamoto
Publikováno v:
Journal of the American College of Cardiology. 80:2239-2250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3cad2a98fe0475569cf828de52fabee
https://doi.org/10.1016/j.jacc.2022.09.032
https://doi.org/10.1016/j.jacc.2022.09.032
Autor:
Eleanor L. Schuchardt, Shelley D. Miyamoto, Timothy Crombleholme, Anis Karimpour-Fard, Armin Korst, Bonnie Neltner, Lisa W. Howley, Bettina Cuneo, Carmen C. Sucharov
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 2, p 37 (2022)
Twin-twin transfusion syndrome (TTTS) is a rare but serious cause of fetal cardiomyopathy with poorly understood pathophysiology and challenging prognostication. This study sought a nonbiased, comprehensive assessment of amniotic fluid (AF) microRNAs
Externí odkaz:
https://doaj.org/article/d98e16157dc3451a9d7d45306901f0a4
Autor:
Lee S. Toni, Anastacia M. Garcia, Danielle A. Jeffrey, Xuan Jiang, Brian L. Stauffer, Shelley D. Miyamoto, Carmen C. Sucharov
Publikováno v:
MethodsX, Vol 5, Iss , Pp 599-608 (2018)
Accurate and reliable analysis of gene expression depends on the extraction of pure and high-quality RNA. However, while the conventional phenol-chloroform RNA extraction is preferable over silica-based columns, particularly when cost is a concern or
Externí odkaz:
https://doaj.org/article/5a078beb2b974de99a8bef2278049806
Autor:
Claire Fraley, Sarah A. Milgrom, Lavanya Kondapalli, Matthew R. G. Taylor, Luisa Mestroni, Shelley D. Miyamoto
Publikováno v:
Children, Vol 8, Iss 9, p 829 (2021)
Cardiotoxicity is a well-recognized late effect among childhood cancer survivors. With various pediatric cancers becoming increasingly curable, it is imperative to understand the disease burdens that survivors may face in the future. In order to prev
Externí odkaz:
https://doaj.org/article/7b0a99e72a9a4d069e1e03997b8c7cae
Autor:
Carmen C. Sucharov, Bonnie Neltner, Ashley E. Pietra, Anis Karimpour-Fard, Joshen Patel, Carolyn Y. Ho, Shelley D. Miyamoto
Publikováno v:
Circulation: Heart Failure.
Background: Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiomyopathy. Pathogenic germline variation in genes encoding the sarcomere is the predominant cause of disease. However diagnostic features, including unexplained left ventri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaaaf638c5b1fac1378aaeceeb8b0171
https://doi.org/10.1161/circheartfailure.122.010291
https://doi.org/10.1161/circheartfailure.122.010291
Autor:
Anastacia M. Garcia, Lee S. Toni, Carissa A. Miyano, Genevieve C. Sparagna, Raleigh Jonscher, Elisabeth K. Phillips, Anis Karimpour-Fard, Hailey L. Chapman, Angela N. Baybayon-Grandgeorge, Ashley E. Pietra, Emma Selner, Kathryn C. Chatfield, Brian L. Stauffer, Carmen C. Sucharov, Shelley D. Miyamoto
Publikováno v:
JACC Basic Transl Sci
The mechanisms responsible for heart failure in single-ventricle congenital heart disease are unknown. Using explanted heart tissue, we showed that failing single-ventricle hearts have dysregulated metabolic pathways, impaired mitochondrial function,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b25e81ba6d74f1c7b7562e8e4b66f2
https://europepmc.org/articles/PMC10077120/
https://europepmc.org/articles/PMC10077120/
Autor:
Asma K. Omar, Lisa M. Wolfe, Kathryn C. Chatfield, Adam J. Chicco, Shelley D. Miyamoto, Luke A. Whitcomb, Kalyn S. Specht, Genevieve C. Sparagna
Publikováno v:
Journal of Inherited Metabolic Disease. 45:111-124
Barth syndrome (BTHS) is an X-linked disorder that results from mutations in the TAFAZZIN gene, which encodes a phospholipid transacylase responsible for generating the mature form of cardiolipin in inner mitochondrial membranes. BTHS patients develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c02911bd9c9ea8d58727c28258620062
https://doi.org/10.1002/jimd.12459
https://doi.org/10.1002/jimd.12459