Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M A Casolaro"'
Publikováno v:
American Review of Respiratory Disease. 137:406-411
Langerhans' cells are a defined subpopulation of the mononuclear phagocyte system known to accumulate in the lung in histiocytosis X, an interstitial lung disorder strongly linked to cigarette smoking. To evaluate the hypothesis that cigarette smokin
Publikováno v:
Proceedings of the National Academy of Sciences. 86:680-684
To evaluate the possibility of administering therapeutic proteins via the respiratory route, we administered an aerosol of recombinant DNA-produced human alpha 1-antitrypsin (rAAT) to anesthetized sheep and measured levels of the protein in epithelia
Autor:
F Ogushi, David T. Curiel, R C Hubbard, Mark L. Brantly, G A Fells, M A Casolaro, Ronald G. Crystal
Publikováno v:
American Review of Respiratory Disease. 137:364-370
S-type alpha 1-antitrypsin (alpha 1AT) is a deficiency haplotype that differs from the common normal M1 (val213) alpha 1AT haplotype by a single amino acid (glu264 to val264). To evaluate the adequacy of the antineutrophil elastase protection associa
Autor:
J T Wittes, S E Sellers, Mark D. Wewers, K M McPhaul, Ronald G. Crystal, M A Casolaro, S C Swayze
Publikováno v:
New England Journal of Medicine. 316:1055-1062
In patients with alpha 1-antitrypsin deficiency, the development of emphysema is believed to be caused by the unchecked action of proteases on lung tissue. We evaluated the feasibility, safety, and biochemical efficacy of intermittent infusions of al
Publikováno v:
The American review of respiratory disease. 135(2)
Tamoxifen, an agent that binds to intracytoplasmic estrogen receptors, was evaluated as a possible means of increasing alpha-1-antitrypsin (alpha 1AT) synthesis and/or secretion and thus alpha 1AT serum levels in subjects with the homozygous form of
Autor:
M. A. Casolaro, G. Fells, M. Wewers, J. E. Pierce, F. Ogushi, R. Hubbard, S. Sellers, J. Forstrom, D. Lyons, G. Kawasaki, al. et
Publikováno v:
Journal of applied physiology (Bethesda, Md. : 1985). 63(5)
To evaluate the potential use of recombinant DNA-produced alpha-1-antitrypsin (alpha-1-AT) to augment the lung antineutrophil elastase defenses in alpha-1-AT deficiency, we compared the kinetics of intravenously administered recombinant produced alph
Publikováno v:
The American review of respiratory disease. 135(3)
The null-null phenotype of alpha 1-antitrypsin (alpha 1AT), a phenotype characterized by no detectable alpha 1AT in serum, presents a rare opportunity to examine the contribution of alpha 1AT to the antineutrophil elastase protection of the lower res