Výsledky vyhledávání - "Charles J Gauntt"

Autor: S. Tracy, Nora M. Chapman, Charles J. Gauntt

The coxsackieviruses are the best-studied group of nonpolio enteroviruses. Unlike that of the polioviruses, the immune reactions of the human or murine (in models of human disease) hosts of infections by the coxsackieviruses are an important componen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::950b553058f2428ac536e1727d2442f0
https://doi.org/10.1128/9781555817916.ch31

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Antigenic Mimicry between Self and Coxsackievirus Proteins Leads to Both Humoral and Cellular Autoimmunity to Heart Proteins

Autor: Charles J. Gauntt, Sally A. Huber

Enteroviruses have evolved mechanisms for terminal shutoff of host protein synthesis. These mechanisms involve viral protease 2A degradation of the cellular p220 protein cap-dependent binding complex or degradation of poly(A)-binding protein. These m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::065f07ad4cdfcba6f3cc1ea888e31bdc
https://doi.org/10.1128/9781555818074.ch5

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Group B coxsackievirus myocarditis and pancreatitis: Connection between viral virulence phenotypes in mice

Autor: Steven Tracy, Pascale H. Lane, Sara M. Reyna, Charles J. Gauntt, Katja Höfling, Samuel J. Pirruccello

Publikováno v: Journal of Medical Virology. 62:70-81

The group B coxsackieviruses (CVB) induce experimental pancreatitis and myocarditis in mice and are established agents of human myocarditis, especially in children. We tested the hypothesis that the development of CVB-induced myocarditis is linked to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::40c8015b59556cad6913f78029108f7c
https://doi.org/10.1002/1096-9071(200009)62:1<70::aid-jmv11>3.0.co

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Aloe polymannose enhances anti-coxsackievirus antibody titres in mice

Autor: Charles J. Gauntt, B. H. McAnalley, H. J. Wood, H. R. McDaniel

Publikováno v: Phytotherapy Research. 14:261-266

Aloe polymannose (AP), a high mannose biological response modifier (BRM) purified from the Aloe barbadensis Miller plant, was tested for activity in enhancing antibody titres against coxsackievirus B3 (CVB3) and CVB3-induced myocarditis in murine mod

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::594d311fd6299289b4b874c18bdea992
https://doi.org/10.1002/1099-1573(200006)14:4<261::aid-ptr579>3.0.co

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Protection from glutathione depletion by a glyconutritional mixture of saccharides

Autor: Charles J. Gauntt, B. McAnalley, Rola Barhoumi, Robert C. Burghardt, H. R. McDaniel, David L. Busbee

Publikováno v: Scopus-Elsevier

A complex glyconutritional (GN) mixture of mono-, di-and polysaccharides was investigated to assess its capacity to protect two different types of rodent cells, rat hepatocytes and mouse splenocytes, from depletion of glutathione by a sulfhydryl-reac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe67846cd51fa3feaa5ec6f5c4510f3
https://doi.org/10.1007/s11357-999-0018-z

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Cardiovirulent Coxsackieviruses and the Decay-Accelerating Factor (CD55) Receptor

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef10df6bc2c495c2b1efd768af581b80
https://doi.org/10.1006/viro.1998.9122

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Genomic regions of coxsackievirus B3 associated with cardiovirulence

Autor: Charles J. Gauntt, Nora M. Chapman, Cheol Lee, Elizabeth Maull, S. Tracy

Publikováno v: Journal of Medical Virology. 52:341-347

The molecular basis for cardiovirulence in the coxsackievirus B3 (CVB3) genome was examined in a murine model of acute myocarditis. Infectious cDNAs representing a highly cardiovirulent coxsackievirus B3 (CVB3m) and a noncardiovirulent (CVB30) virus

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f036363140ce8867be36b843dfda965a
https://doi.org/10.1002/(sici)1096-9071(199707)52:3<341::aid-jmv18>3.0.co

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