Zobrazeno 1 - 10
of 307
pro vyhledávání: '"A. B. Hinton"'
Autor:
Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
Background Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with CMA abnormalities have been inconsistent, which ma
Externí odkaz:
https://doaj.org/article/3ce4e66e20b2416085e8144a51318ce2
Autor:
Jennifer B. Hinton
Publikováno v:
Journal of Political Ecology, Vol 27, Iss 1, Pp 236-262 (2020)
This conceptual article contributes to the post-growth strand of political ecology literature, which seeks to find sustainable ways of organizing the economy that do not require economic growth. It explores the idea that transitioning to post-growth
Externí odkaz:
https://doaj.org/article/0dfca272c9844e9c86fbfa01394bec8d
Autor:
Benjamin J. Landis, Dongbing Lai, Dong-Chuan Guo, Joel S. Corvera, Muhammad T. Idrees, Henry W. Stadler, Christian Cuevas, Gavin U. Needler, Courtney E. Vujakovich, Dianna M. Milewicz, Robert B. Hinton, Stephanie M. Ware
Publikováno v:
HGG Advances, Vol 3, Iss 1, Pp 100057- (2022)
Summary: Thoracic aortic aneurysm (TAA) predisposes to sudden, life-threatening aortic dissection. The factors that regulate interindividual variability in TAA severity are not well understood. Identifying a molecular basis for this variability has t
Externí odkaz:
https://doaj.org/article/60059b4211c04ccaaf92dff1bc736065
Publikováno v:
Annals of Occupational and Environmental Medicine, Vol 30, Iss 1, Pp 1-10 (2018)
Abstract Background The nature of police work often necessitates use of Individual Light Armour Vests (ILAVs) for officer protection. Previous research has demonstrated various biomechanical and physical performance impacts of ILAVs, however, little
Externí odkaz:
https://doaj.org/article/3ab1fd781119482e970243e7fa2f035b
Publikováno v:
IMA Journal of Applied Mathematics. 87:804-851
We derive conditions for a one-term fourth-order Sturm–Liouville operator on a finite interval with one singular endpoint to have essential spectrum equal to $[0,\infty )$ or $\varnothing $. Of particular usefulness are Kummer–Liouville transform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b80655fc0e1ab15c396f29493f2bc96
https://doi.org/10.1093/imamat/hxac021
https://doi.org/10.1093/imamat/hxac021
Autor:
Robert B. Hinton, Amy L. Juraszek, Amy M. Opoka, Benjamin J. Landis, J. Michael Smith, Robert P. Mecham, Kevin E. Bove
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 8, Iss 7, p 75 (2021)
Elastic fiber fragmentation (EFF) is a hallmark of aortic valve disease (AVD), and neovascularization has been identified as a late finding related to inflammation. We sought to characterize the relationship between early EFF and aberrant angiogenesi
Externí odkaz:
https://doaj.org/article/195740bf63654f3191c2ec4432d9a37a
Publikováno v:
Applicable Analysis. 101:1659-1681
We study a Sturm–Liouville problem in the cross-section of the ocean waveguide covered by pack ice. We prove the basis properties of the eigenfunctions, the convergence of the corresponding Fourier...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7b0bbd1c7d27825762feb764a0402aa
https://doi.org/10.1080/00036811.2021.1988580
https://doi.org/10.1080/00036811.2021.1988580
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 2, Iss 3, Pp 190-199 (2015)
Turner syndrome (TS), most frequently caused by X-monosomy (45,X), is characterized in part by cardiovascular abnormalities, including aortopathy and bicuspid aortic valve (BAV). There is a need for animal models that recapitulate the cardiovascular
Externí odkaz:
https://doaj.org/article/0764d810f382416aac9b5dcc306a034c
Autor:
Robert B. Hinton, Kim L. McBride, Steven B. Bleyl, Neil E. Bowles, William L. Border, Vidu Garg, Teresa A. Smolarek, Seema R. Lalani, Stephanie M. Ware
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 2, Iss 2, Pp 76-92 (2015)
Cardiovascular malformations (CVMs) are the most common birth defect, occurring in 1%–5% of all live births. Although the genetic contribution to CVMs is well recognized, the genetic causes of human CVMs are identified infrequently. In addition, a
Externí odkaz:
https://doaj.org/article/61b454d754e540f9ab448512c708dd17
Autor:
Richard C. Godby, Charu Munjal, Amy M. Opoka, J. Michael Smith, Katherine E. Yutzey, Daria A. Narmoneva, Robert B. Hinton
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 1, Iss 3, Pp 237-256 (2014)
Aortic valve disease is a burgeoning public health problem associated with significant mortality. Loss of function mutations in NOTCH1 cause bicuspid aortic valve (BAV) and calcific aortic valve disease. Because calcific nodules manifest on the fibro
Externí odkaz:
https://doaj.org/article/3e8b463d518d488e98206e73c2a0537c