Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lawrence H. Chow"'
Autor:
J. Geoffrey Pickering, Stephen M. Sims, Lawrence H. Chow, Eric van der Veer, Caroline Van Den Diepstraten, Yao Shan Fan, Shaohua Li
Publikováno v:
Circulation Research. 89:517-525
Abstract— Vascular smooth muscle cells (SMCs) perform diverse functions and this functional heterogeneity could be based on differential recruitment of distinct SMC subsets. In humans, however, there is little support for such a paradigm, partly be
Publikováno v:
Journal of Biological Chemistry. 275:35384-35392
To migrate in the vessel wall, smooth muscle cells (SMCs) must contend with abundant type I collagen. We investigated the mechanisms used by human SMCs to efficiently migrate on type I collagen, following stimulation with fibroblast growth factor-2 (
Autor:
Lawrence H. Chow, Bosco M.C. Chan, Kem A. Rogers, Shaohua Li, J. Geoffrey Pickering, Edward F. Rocnik, Robert Zhong
Publikováno v:
The American Journal of Pathology. 156:453-465
Fibronectin is secreted from the cell as a soluble protein that must then polymerize to regulate cell function. To elucidate the process of fibronectin matrix assembly in vascular disease, we immunostained sections of balloon-injured rat carotid arte
Autor:
Tami A. Martino, Christopher D. Richardson, Charles J. Gauntt, Martin Petric, Peter P. Liu, Karen Aitken, Martha Brown, Lawrence H. Chow
Publikováno v:
Virology. 244:302-314
Group B coxsackieviruses are etiologically linked with many human diseases including acute myocarditis and associated chronic dilated cardiomyopathy. Well-established CVB3 cardiovirulent strains (CVB3c (s) ) with known phenotypic differences have bee
Publikováno v:
ResearcherID
Background The major threat to the long-term survival of cardiac allograft recipients is the development of diffuse intimal thickening in the allograft coronary arteries through mechanisms that are poorly understood. Although antidonor antibodies hav
Publikováno v:
The American Journal of Cardiology. 78:633-637
The pattern of collagen deposition after coronary angioplasty could significantly influence recurrent lesion formation. Traditional histologic assessments of coronary restenosis lesions have not identified abundant collagen fibers in restenotic tissu
Autor:
M. A. Beck, Nora M. Chapman, K. Klingel, Lawrence H. Chow, Stanley J. Radio, Bruce M. McManus, R. Kandolf, S. M. Tracy
Publikováno v:
European Heart Journal. 12:18-21
The pathological diagnosis of myocarditis rests on well-described histopathological criteria. Appreciation for the disease-specific sensitivity of the endomyocardial biopsy, as well as the phenotypical and functional nature of inflammatory infiltrate
Autor:
Ranjan K. Thakur, Lawrence H. Chow, Peter V. Pflugfelder, William J. Kostuk, James E. Brown, Gerard M. Guiraudon, Collette M. Guiraudon
Publikováno v:
Journal of Cardiac Surgery. 10:295-297
Latissimus dorsi cardiomyoplasty is a promising surgical therapy in some patients with congestive heart failure. Although the mortality in heart failure patients is attributable primarily to heart failure and ventricular arrhythmias, the mechanism of
Autor:
Robert Zhong, G. Melville Williams, Jing Li, Xiaozhou Han, Lawrence H. Chow, Jifu Jiang, J. Geoffrey Pickering
Intimal expansion by vascular smooth muscle cells (SMCs) is a characteristic feature of graft vascular disease. Whether graft intimal SMCs arise from donor or recipient tissue is not well established but has important pathogenetic implications. We ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74af018ac6d794ca0ce29227d8a7a871
https://europepmc.org/articles/PMC1891984/
https://europepmc.org/articles/PMC1891984/
Autor:
J. Fish, S. Uniyal, J. G. Pickering, T. Chau, M. A. Laurin, Christopher G. Ellis, Bosco M.C. Chan, Lawrence H. Chow, C. M. Ford
Publikováno v:
Circulation research. 80(5)
Abstract Fibroblast growth factor-2 (FGF-2) has been implicated in vascular smooth muscle cell (SMC) migration, a key process in vascular disease. We demonstrate here that FGF-2 promotes SMC motility by altering β 1 integrin–mediated interactions