Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M. J. Schlosser"'
Publikováno v:
InflammoPharmacology. 12:33-45
Constitutive and inducible isoforms of nitric oxide synthase (NOS) catalyze the synthesis of nitric oxide (NO) from L-arginine in various tissues and in different pathophysiologic states. Short-term treatment with NOS inhibitors has been associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cec646578dccfca99fd32b557ed90818
https://doi.org/10.1163/156856004773121356
https://doi.org/10.1163/156856004773121356
Publikováno v:
Toxicological Sciences. 35:197-204
Many marketed pharmaceuticals are known to cause idiosyncratic agranulocytosis in humans. Similarly prinomide, an antiinflammatory drug, was associated with a low incidence of agranulocytosis ( 90%; 2 min); this reaction was dependent on H2O2and MPO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc5b457d87748de324a5bb5c98cf8408
https://doi.org/10.1093/toxsci/35.2.197
https://doi.org/10.1093/toxsci/35.2.197
Publikováno v:
Neurotoxicity research. 3(3)
Hippocampal neurodegeneration and glia response was examined following administration of the nitric oxide synthase inhibitor, Nomega-nitro-L-arginine methyl ester (L-NAME). Male Long-Evans rats received L-NAME (50 mg/kg, ip) either once or twice a da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df46f449e1046cea2286eb0f49d00eb2
https://pubmed.ncbi.nlm.nih.gov/15111256
https://pubmed.ncbi.nlm.nih.gov/15111256
Publikováno v:
Fundamental and applied toxicology : official journal of the Society of Toxicology. 35(2)
Many marketed pharmaceuticals are known to cause idiosyncratic agranulocytosis in humans. Similarly prinomide, an antiinflammatory drug, was associated with a low incidence of agranulocytosis (0.3%) in clinical trials, even though chronic toxicity st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5fb4317036478ce84aad0fe0b65a9f2
https://pubmed.ncbi.nlm.nih.gov/9038241
https://pubmed.ncbi.nlm.nih.gov/9038241
Publikováno v:
Molecular biology and evolution. 12(5)
A phylogenetic survey using the polymerase chain reaction (PCR) has identified four major P element subfamilies in the saltans and willistoni species groups of Drosophila. One subfamily, containing about half of the sequences studied, consists of ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df896a53f199bf7f584d6e3ff1104cc
https://pubmed.ncbi.nlm.nih.gov/7476136
https://pubmed.ncbi.nlm.nih.gov/7476136
Publikováno v:
NMR in biomedicine. 4(1)
The progression of carbon tetrachloride-induced liver damage, determined by 31P NMR spectroscopy, was compared with selected serum enzyme and histological changes in rats. ATP levels declined as early as 8 h post-CCI4 administration, with partial rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29a2089ecd0007eafa931c7b497ccdf6
https://pubmed.ncbi.nlm.nih.gov/2029455
https://pubmed.ncbi.nlm.nih.gov/2029455
Publikováno v:
Proceedings of the JFPS International Symposium on Fluid Power. 1989:41-51
A brief survey is given of the scope of the design of displacement pumps and hydromotors which are used in the realisation of hydrostatic power transmissions.During the recent 25 years the computer is playing a role of ever increasing importance in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b2fcd8f775202d4f785bac321600dfd
https://doi.org/10.5739/isfp.1989.41
https://doi.org/10.5739/isfp.1989.41
Autor:
M J, Schlosser, A J, Verlangieri
Publikováno v:
Artery. 15(6)
A novel short-term organ culture system was used to evaluate intimal permeability changes by measuring aortic [14C]methylated albumin accumulation. Aortic plugs were removed from the upper thoracic aorta of male guinea pigs and maintained in serum-fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f100dd7ff57ac8761662880c1641019
https://pubmed.ncbi.nlm.nih.gov/3178505
https://pubmed.ncbi.nlm.nih.gov/3178505