TY  - JOUR
A1  - Kühnel, Dana
A1  - Steinberg, Pablo
A1  - Scholtka, Bettina
T1  - A human-relevant dose of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PHIP) can induce precancerous lesions in rat intestine after 6 months of exposure
Y1  - 2004
SN  - 0028-1298
ER  - 
TY  - JOUR
A1  - Thierbach, René
A1  - Drewes, Gunnar
A1  - Fusser, Markus
A1  - Wolfrum, Kathrin
A1  - Epe, Bernd
A1  - Ristow, Michael
A1  - Steinberg, Pablo
T1  - A role for iron-sulfur cluster proteins in DNA repair
Y1  - 2009
UR  - http://www.springerlink.com/content/100530
U6  - https://doi.org/10.1007/s00210-009-0404-1
SN  - 0028-1298
ER  - 
TY  - JOUR
A1  - Volohonsky, Gloria
A1  - Tuby, Chen N. Y. H.
A1  - Porat, Noga
A1  - Wellman-Rousseau, Maria
A1  - Visvikis, Athanase
A1  - Leroy, Pierre
A1  - Rashi, Sharon
A1  - Steinberg, Pablo
A1  - Stark, Avishay Abraham
T1  - A spectrophotometric assay of gamma-glutamylcysteine synthetase and glutathione synthetase in crude extracts from tissues and cultured mammalian cells
Y1  - 2002
ER  - 
TY  - JOUR
A1  - Steinberg, Pablo
A1  - Fischer, Thomas M.
A1  - Arand, Michael
A1  - Park, Eunju
A1  - Elmadfa, Ibrahim
A1  - Rimkus, Gerhard
A1  - Brunn, Hubertus
A1  - Dienes, Hans-Peter
T1  - Acute hepatotoxicity of the polycyclic musk 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthaline (AHTN)
Y1  - 1999
ER  - 
TY  - JOUR
A1  - Mazurek, Sybille
A1  - Eigenbrodt, Erich
A1  - Failing, Klaus
A1  - Steinberg, Pablo
T1  - Alterations in the glycolytic and glutaminolytic pathways after malignant transformation of rat liver oval cells
Y1  - 1999
ER  - 
TY  - JOUR
A1  - Thierbach, René
A1  - Blume, Urte
A1  - Wolfrum, K.
A1  - Drewes, Gunnar
A1  - Voigt, Anja
A1  - Ristow, Michael
A1  - Steinberg, Pablo
T1  - Altered carbohydrate metabolism in a tumour developing knock-out mice model
Y1  - 2010
UR  - http://www.springerlink.com/content/100530
U6  - https://doi.org/10.1007/s00210-010-0508-7
SN  - 0028-1298
ER  - 
TY  - JOUR
A1  - Hengstler, Jan Georg
A1  - Utesch, D.
A1  - Steinberg, Pablo
T1  - Cryopreserved primary hepatocytes as a constantly available in vitro model for the evaluation of human and animal drug metabolism and enzyme induction
Y1  - 2000
ER  - 
TY  - JOUR
A1  - Hengstler, Jan Georg
A1  - Ringel, M.
A1  - Biefang, Katja
A1  - Hammel, S.
A1  - Milbert, U.
A1  - Gerl, M.
A1  - Klebach, M.
A1  - Diener, B.
A1  - Platt, Karl-Ludwig
A1  - Böttger, Thomas
A1  - Steinberg, Pablo
A1  - Oesch, Franz
T1  - Cultures with cryopreserved hepatocytes : applicability for studies of enzyme induction
Y1  - 2000
ER  - 
TY  - JOUR
A1  - Steinberg, Pablo
A1  - Fischer, Thomas M.
A1  - Kiulies, Sandra
A1  - Biefang, Katja
A1  - Platt, Karl-Ludwig
A1  - Oesch, Franz
A1  - Böttger, Thomas
A1  - Bulitta, Clemens
A1  - Kempf, Peter
A1  - Hengstler, Jan Georg
T1  - Drug metabolizing capacity of cryopreserved human, rat and mouse liver parenchymal cells in suspension
Y1  - 1999
ER  - 
TY  - JOUR
A1  - Bartsch, Ingrid
A1  - Zschaler, Ingrid
A1  - Haseloff, Monika
A1  - Steinberg, Pablo
T1  - Establishment of a long-term culture system for rat colon epithelial cells
N2  - The aim of this study was to establish a long-term culture. system for rat colon epithelia isolaled by incubating a 4-cm-long rat colon segment cut longitudinally with all ethylenediaminetetraacetic acid [disodium salt]- containing buffer, taken up in conditioned medium from the normal rat kidney fibroblast cell line NRK (i.e., the supernatant Of pure NRK cultures), directly plated on mitomycin C-treated NRK cells and subcultured with conditioned medium from NRK cells. Cells started to migrate out of the crypts shortly after plating them on NRK feeder layers. Some of the crypts fell apart during the isolation procedure. whereas the vast majority of them did it within I to 2 Ill after plating. The cells proliferated extremely slowly but continuously over a period of 4 mo and were epithelial because they expressed cytokeratin 19 and were stained by crystal violet at pH 2.8. In conclusion, the experimental system described ill this study allows to maintain rat colon epithelial cells for up to 4 mo in culture and can be used to Study the effects of a variety of tumor-modulating factors on growth and gene expression of normal colon epithelial cells in vitro
Y1  - 2003
UR  - http://www.springerlink.com/content/120498/
U6  - https://doi.org/10.1290/0404035.1
SN  - 1071-2690
ER  -