Zobrazeno 1 - 10
of 54
pro vyhledávání: '"K W, Bock"'
Publikováno v:
The Aeronautical Journal. 101:421-428
The transonic facility of DLR Göttingen (TWG) has been modernised with respect to an improved flow quality and flow simulation, as well as to the logistics of exchangeable test sections, operational reliability and productivity. It is presently equi
Autor:
H. Holst, K.-W. Bock
Publikováno v:
ICIASF'97 Record. International Congress on Instrumentation in Aerospace Simulation Facilities.
The transonic wind tunnel TWG of DLR Gottingen has been modernized with respect to an improved flow quality as well as to the logistics of exchangeable test sections, operational reliability and productivity. It is presently equipped with a Laval noz
Publikováno v:
Toxicology and applied pharmacology. 183(2)
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is the most potent tumor promoter ever tested in rodents. Although it is known that most of TCDD actions are mediated by binding to the aryl hydrocarbon receptor (AhR), the mechanisms leading to tumor promot
Publikováno v:
New Results in Numerical and Experimental Fluid Mechanics III ISBN: 9783642536427
In the Transonic Wind Tunnel Gottingen (DNW-TWG) a test campaign was carried out to obtain experimental pressure data for a continuously rolling delta-wing-model. This campaign includes the design and manufacture of the model and the rolling apparatu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc8fe46e8d39734f34fd9f4416515ba3
https://doi.org/10.1007/978-3-540-45466-3_13
https://doi.org/10.1007/978-3-540-45466-3_13
Autor:
J M, Wong, P A, Harper, U A, Meyer, K W, Bock, K, Morike, J, Lagueux, P, Ayotte, R F, Tyndale, E M, Sellers, D K, Manchester, A B, Okey
Publikováno v:
Pharmacogenetics. 11(1)
The aryl hydrocarbon receptor (AHR) is a ligand-dependent transcriptional regulator of several genes including the cytochrome P4501 (CYP1) family as well as genes encoding factors involved in cell growth and differentiation. In mice, several polymorp
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 27(5)
Human colon carcinoma Caco-2 cells were used to study the induction of UDP glucuronosyltransferase (UGT) isoforms UGT1A6, UGT1A9, and UGT2B7 by aryl hydrocarbon receptor agonists and by antioxidant-type inducers with 2,3,7,8-tetrachlorodibenzo-p-diox
Autor:
Thierry Fol, V. Selmin, J. M. Alonso, J. M. de la Viuda, A. Abbas, Luciano Fornasier, Helmuth Schwarten, J. Periaux, B. Stoufflet, K.-W. Bock, W. Haase, Patrick Le Tallec, Olivier Pironneau, Alain Dervieux, Nathalie Marco, Jean-Michel Malé, Th. E. Labrujère, H. Kuiper, A. J. van der Wees, C. F. W. Hendriks, P. Chaviaropoulos, V. Dedoussis, K. D. Papailiou, G. Bugeda, E. Oñate
Publikováno v:
Notes on Numerical Fluid Mechanics (NNFM) ISBN: 9783322901958
The following sections contain the different contributions from the ECARP consortium to the resolution of the workshop test cases defined in section II. Each contribution contains a theoretical description of the optimization technique used by each p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bddb6116b62c7bb368b5d4de1932be1d
https://doi.org/10.1007/978-3-322-90193-4_3
https://doi.org/10.1007/978-3-322-90193-4_3
Autor:
K W, Bock
Publikováno v:
Humanexperimental toxicology. 15(10)
Autor:
K. W. Bock, W. Lilienblum
Publikováno v:
Handbook of Experimental Pharmacology ISBN: 9783642784316
Roles of isozymes of the uridine diphosphate (UDP)-glueuronosyltransferase (UGT) family (EC 2.4.1.17) will be discussed in the light of recent concepts of carcinogenesis. Glucuronides may be transport forms of carcinogens that play a major role in de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de61e3c5d7126e16920f1a4363604fff
https://doi.org/10.1007/978-3-642-78429-3_14
https://doi.org/10.1007/978-3-642-78429-3_14
Autor:
K W, Bock
Publikováno v:
Reviews of physiology, biochemistry and pharmacology. 125
1. The AhR represents a ligand-activated transcription factor. Receptor agonists include planar aromatic compounds, a variety of heterocyclic plant constituents, and PCDD/PCDF. The latter lead to persistent activation of the receptor due to their str