Zobrazeno 1 - 10
of 671
pro vyhledávání: '"C Lancaster"'
Autor:
Megan C. Lancaster, Hung-Hsin Chen, M. Benjamin Shoemaker, Matthew R. Fleming, Teresa L. Strickland, James T. Baker, Grahame F. Evans, Hannah G. Polikowsky, David C. Samuels, Chad D. Huff, Dan M. Roden, Jennifer E. Below
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract Rare genetic diseases are typically studied in referral populations, resulting in underdiagnosis and biased assessment of penetrance and phenotype. To address this, we develop a generalizable method of genotype inference based on distant rel
Externí odkaz:
https://doaj.org/article/70c43e12db9146dda536866ebc72828a
Autor:
Daniel R. Tabet, Da Kuang, Megan C. Lancaster, Roujia Li, Karen Liu, Jochen Weile, Atina G. Coté, Yingzhou Wu, Robert A. Hegele, Dan M. Roden, Frederick P. Roth
Publikováno v:
Genome Biology, Vol 25, Iss 1, Pp 1-14 (2024)
Abstract Background Computational variant effect predictors offer a scalable and increasingly reliable means of interpreting human genetic variation, but concerns of circularity and bias have limited previous methods for evaluating and comparing pred
Externí odkaz:
https://doaj.org/article/be0e465c42924e5dbc503b50ed990281
Autor:
Lin-Mei Zhao, Andrew C. Lancaster, Ritesh Patel, Helen Zhang, Tim Q. Duong, Zhicheng Jiao, Cheng Ting Lin, Terrance Healey, Thaddeus Wright, Jing Wu, Harrison X. Bai
Publikováno v:
Heliyon, Vol 10, Iss 11, Pp e31751- (2024)
Purpose: The purpose of this study is to identify clinical and imaging characteristics associated with post-COVID pulmonary function decline. Methods: This study included 22 patients recovering from COVID-19 who underwent serial spirometry pulmonary
Externí odkaz:
https://doaj.org/article/70e4bdc599a742e3832c435724c7d379
Autor:
Guillermo Torres, Andrew C. Lancaster, Jun Yang, Megan Griffiths, Stephanie Brandal, Rachel Damico, Dhananjay Vaidya, Catherine E. Simpson, Lisa J. Martin, Michael W. Pauciulo, William C. Nichols, David D. Ivy, Eric D. Austin, Paul M. Hassoun, Allen D. Everett
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 3, Pp n/a-n/a (2023)
Abstract Insulin‐like growth factor (IGF) binding proteins (IGFBPs) are a family of growth factor modifiers, some of which are known to be independently associated with pulmonary arterial hypertension (PAH) survival. IGF factor binding protein 7 (I
Externí odkaz:
https://doaj.org/article/9d104d23bbbd4d9993ff27a2919093a7
Autor:
Lynne C. Lancaster
This book studies six vaulting techniques employed in architecture outside of Rome and asks why they were invented where they were and how they were disseminated. Most of the techniques involve terracotta elements in various forms, such as regular fl
Autor:
John C. Meadows, Theresa C. Lancaster, Graham J. Buttrick, Alicja M. Sochaj, Liam J. Messin, Maria del Mar Mora-Santos, Kevin G. Hardwick, Jonathan B.A. Millar
Publikováno v:
Cell Reports, Vol 18, Iss 6, Pp 1422-1433 (2017)
The onset of anaphase is triggered by activation of the anaphase-promoting complex/cyclosome (APC/C) following silencing of the spindle assembly checkpoint (SAC). APC/C triggers ubiquitination of Securin and Cyclin B, which leads to loss of sister ch
Externí odkaz:
https://doaj.org/article/0bc62b9d3867448eaa943b9307342254
Akademický článek
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Akademický článek
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Autor:
J. Lukas Laws, Megan C. Lancaster, M. Ben Shoemaker, William G. Stevenson, Rebecca R. Hung, Quinn Wells, D. Marshall Brinkley, Sean Hughes, Katherine Anderson, Dan Roden, Lynne W. Stevenson
Publikováno v:
Circ Res
There is increasing evidence regarding the prevalence of genetic cardiomyopathies, for which arrhythmias may be the first presentation. Ventricular and atrial arrhythmias presenting in the absence of known myocardial disease are often labelled as idi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93adf12a19632321cb215bc0f68715ef
https://doi.org/10.1161/circresaha.122.319835
https://doi.org/10.1161/circresaha.122.319835
Autor:
Megan C. Lancaster, Hung-Hsin Chen, M. Benjamin Shoemaker, Matthew R. Fleming, James T. Baker, Hannah G. Polikowsky, David C. Samuels, Chad D. Huff, Dan M. Roden, Jennifer E. Below
ImportanceThe diagnosis and study of rare genetic disease is often limited to referral populations, leading to underdiagnosis and a biased assessment of penetrance and phenotype.ObjectiveTo develop a generalizable method of genotype inference based o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a3148e78ab754b441ce5dd66a82bb2
https://doi.org/10.1101/2023.04.19.23288831
https://doi.org/10.1101/2023.04.19.23288831