Zobrazeno 1 - 10
of 270
pro vyhledávání: '"D, Mercola"'
Autor:
K. Schütze, H. Kremling, F. Lasitschka, D. Mercola, J. Rassweiler, W. Lernhardt, F. Zinnhammer, M. Fiedler, F. Autschbach
Publikováno v:
European Urology Supplements. 15:145-146
Akademický článek
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Publikováno v:
BioTechniques. 29:162-169
A methodology is described that allows the in vivo trapping of transcription factors to their target regulatory elements in multiple genes simultaneously. Cross-linking using formaldehyde is the first of several steps to isolate, purify, clone and ch
Autor:
M. Pfahl, N. Dean, C. Liu, D. Mercola, Y. M. Yang, W. Charbono, R. Mckay, O. Potapova, F. Bost, X. P. Lu
Publikováno v:
Insulin & Related Proteins-Structure to Function and Pharmacology ISBN: 9781402006555
Recent studies have revealed that the alternate Map Kinase pathway, termed the Jun Kinase pathway, is commonly activated by the Epidermal Growth Factor and Serum in a variety of human tumor lines, especially prostate carcinoma. This pathway activates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0542124efa3ecc4ce7e0f93eea00211d
https://doi.org/10.1007/0-306-47582-0_17
https://doi.org/10.1007/0-306-47582-0_17
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 175
Akademický článek
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Autor:
R A, Gjerset, D, Mercola
Publikováno v:
Advances in experimental medicine and biology. 465
Publikováno v:
Methods in enzymology. 314
Methods for the selection and characterization of antisense oligonucleotides for specifically eliminating closely related gene family members are available. High-throughput semiautomated methods using 96-well plate formats and array technology and im
Autor:
R E, Sobol, D L, Shawler, C, Carson, C, Van Beveren, D, Mercola, H, Fakhrai, M A, Garrett, R, Barone, P, Goldfarb, R M, Bartholomew, S, Brostoff, D J, Carlo, I, Royston, D P, Gold
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 5(9)
The purpose of this study was to determine the safety, toxicity, and antitumor immune response following S.C. immunizations with a mixture of irradiated, autologous tumor cells and autologous fibroblasts that were genetically modified to express the
Publikováno v:
Cell growthdifferentiation : the molecular biology journal of the American Association for Cancer Research. 10(8)
We have previously shown, by expression of a nonphosphorylatable dominant inhibitor mutant of c-Jun [cJun(S63A,S73A)], that activation of the NH2-terminal Jun kinase/stress-activated protein kinase by genotoxic damage is required for DNA repair. Here