Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Cindy R. Moomaw"'
Autor:
Jane Blood-Siegfried, Holly S. Lieder, Abraham Nyska, Kristen Geisenhoffer, Burton Shelton, Kelly Cobb, Dori R. Germolec, William Coombs, Cindy R. Moomaw
Publikováno v:
FEMS Immunology and Medical Microbiology. 42:85-93
Data increasingly implicate a possible role of immune and inflammatory responses to infection in sudden infant death syndrome (SIDS). We have previously described a dual challenge model that results in pathology, organ damage, vascular collapse and u
Autor:
Natasha P. Clayton, June K. Dunnick, Po-Chuen Chan, Cindy R. Moomaw, Theodora R. Devereux, Robert C. Sills, T. V. Ton, Hue-Hua L. Hong
Publikováno v:
Toxicology and Applied Pharmacology. 191:227-234
The most prominent neoplastic lesions in mice in the 2-year studies of o -nitrotoluene and riddelliine were hemangiosarcomas. Fifteen o -nitrotoluene-induced hemangiosarcomas of the skeletal muscle, subcutaneous tissue, and mesentery; 12 riddelliine-
Autor:
Abraham Nyska, David G. Allen, Connie A. Cummings, Shyamal D. Peddada, Carolyn F. Moyer, Cindy R. Moomaw, Po C. Chan, Julie F. Foley, David E. Malarkey, Robert R. Maronpot, Greg Travlos
Publikováno v:
Toxicology and Applied Pharmacology. 184:153-164
Riddelliineis a naturally occurring pyrrolizidine alkaloid found in certain poisonous rangeland plants of the western United States. In National Toxicology Program 2-year studies, riddelliine induced high incidences of hemangiosarcoma in the liver of
Autor:
Annette B. Rice, Jennifer L. Ingram, Alisha R. Sessoms, Daniel L. Morgan, Abraham Nyska, Patricia C. Chulada, Darryl C. Zeldin, Cindy R. Moomaw, Alyce Bradbury, Robert Langenbach, James C. Bonner
Publikováno v:
The American Journal of Pathology. 161:459-470
The cyclooxygenase (COX)-2 enzyme has been implicated as an important mediator of pulmonary fibrosis. In this study, the lung fibrotic responses were investigated in COX-1 or COX-2-deficient (-/-) mice following vanadium pentoxide (V(2)O(5)) exposure
Publikováno v:
Archives of Toxicology. 75:618-624
2,4-Hexadienal (2,4-Hx), an unsaturated aldehyde formed by in vivo and in vitro peroxidation of unsaturated lipid induced, in National Toxicology Program (NTP) gavage studies of F344 rats, forestomach hyperplasia in 13-week and 2-year exposures and s
Autor:
Joseph K. Haseman, Joel F. Mahler, Keisuke Ozaki, Matthew L. Nicolette, Abraham Nyska, Cindy R. Moomaw
Publikováno v:
Toxicologic Pathology. 29:440-450
Peroxisome proliferators are non-mutagenic carcinogens in the liver of rodents, acting both as initiators and promoters. The National Toxicology Program (NTP) conducted a study of several peroxisome proliferators (PPs), including Wyeth (WY)-14643 as
Autor:
Abraham Nyska, Amnon Sintov, Cindy R. Moomaw, Berta Brodsky, Uri Wormser, Liat Lomnitski, Robert R. Maronpot
Publikováno v:
Archives of Toxicology. 74:768-774
In a previous study we demonstrated the protective effect of topical iodine as postexposure treatment for sulfur mustard (SM) application. The iodine treatment results in significantly reduced inflammation and necrosis and increased epidermal hyperpl
Autor:
Ronald L. Melnick, Robert C. Sills, Theodora R. Devereux, Cindy R. Moomaw, Gary A. Boorman, Hue-Hua L. Hong
Publikováno v:
Toxicologic Pathology. 28:529-534
1,3-Butadiene is a multisite carcinogen in rodents. Incidences of cardiac hemangiosarcomas were significantly increased in male and female B6C3F1 mice that inhaled 1,3-butadiene (BD) for 2 years. Eleven BD-induced cardiac hemangiosarcomas were examin
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 278:L209-L216
Vanadium pentoxide (V2O5) is a cause of occupational asthma and bronchitis. We previously reported that intratracheal instillation of rats with V2O5causes fibrosis of the lung parenchyma (J. C. Bonner, P. M. Lindroos, A. B. Rice, C. R. Moomaw, and D.
Publikováno v:
The American Journal of Pathology. 155:213-221
The proliferation of myofibroblasts is a central feature of pulmonary fibrosis. In this study we have used tyrosine kinase inhibitors of the tyrphostin class to specifically block autophosphorylation of the platelet-derived growth factor receptor (PD