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of 43
pro vyhledávání: '"Richard A. Parent"'
Autor:
John J. O'neil, Vaja Tchipashvili, Richard J. Parent, Obinna Ugochukwu, Gaurav Chandra, Maria Koulmanda, Dicken Ko, Tatsuo Kawai
Publikováno v:
Cell Transplantation, Vol 12 (2003)
Recent advances in islet cell transplantation have led to insulin independence in a majority of islet transplant recipients. However, there exists a need to overcome the shortage of donor tissue and the necessity for lifelong immunosuppression. Precl
Externí odkaz:
https://doaj.org/article/8ad7582215564914a75d7b0de82ae6de
Autor:
Richard A. Parent
Publikováno v:
International Journal of Toxicology. 32:89-92
Autor:
Richard A. Parent
Comparative Biology of the Normal Lung, Second Edition, offers a rigorous and comprehensive reference for all those involved in pulmonary research. This fully updated work is divided into sections on anatomy and morphology, physiology, biochemistry,
Autor:
Scott A. King, Richard E. Parent
Publikováno v:
Computer Animation and Virtual Worlds. 15:53-61
Autor:
Milan A. Berge, Halina E. Caravello, Richard A. Parent, Laurie C. Wilkes, Mark G. Hennes, Laura J. Servatius, Michele L. Loftus, Dale E. Sharp
Publikováno v:
Journal of Agricultural and Food Chemistry. 49:1639-1647
The metabolism and distribution of [2,3-(14)C]-acrolein were studied in 10 laying hens orally administered 1.09 mg/kg of body weight/day for 5 days. Eggs, excreta, and expired air were collected. The hens were killed 12-14 h after the last dose and e
Autor:
Scott A. King, Richard E. Parent
Publikováno v:
The Journal of Visualization and Computer Animation. 12:107-115
Autor:
Richard A. Parent
Publikováno v:
International Journal of Toxicology. 19:331-373
Autor:
Douglas E. Paust, Margaret K. Schrimpf, Richard A. Parent, Rebecca Doane, Rasmy E. Talaat, Halina E. Caravello, Dale E. Sharp, Sung J. Lee
Publikováno v:
Toxicological Sciences. 43:110-120
The metabolites of [2,3- 14C]acrolein in the urine and feces of Sprague-Dawley rats were identified after either intravenous administration in saline at 2.5 mg/kg or oral administration by gavage as an aqueous solution as either single or multiple do
Publikováno v:
Journal of Applied Toxicology. 16:449-457
The metabolism and disposition of [2,3- 14 C]acrolein was studied in Sprague-Dawley rats after oral or intravenous dosing. Four groups of ten rats (five male and five female) were dosed with radiolabeled acrolein intravenously at 2.5mg kg -1 (Group 2
Publikováno v:
Journal of Applied Toxicology. 16:103-108
Acrolein was tested for mutagenic activity in seven strains of Salmonella typhimurium and one strain of Escherichia coli using a preincubation assay procedure. Cytotoxicity was evident at dosing levels above 33 and 67 micrograms acrolein per plate in