Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alfred M. Engel"'
Autor:
Michael Tacke, Werner Zolg, Hanno Langen, Wolfgang Rösch, Siegbert Rossol, Gerhard Rohr, Thomas Henkel, Josef Rüschoff, Heinz Bodenmüller, Johann Karl, Herbert Andres, Michael Pfeffer, Bernd Schneidinger, Alfred M. Engel, Peter Berndt, Marie-Luise Hagmann, Stefan Palme, Wolfgang Rollinger, Markus Roeßler
Supplementary Table 1 from Identification of Nicotinamide N-Methyltransferase as a Novel Serum Tumor Marker for Colorectal Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d44a00c9576c73a35538014f3363572
https://doi.org/10.1158/1078-0432.22440960.v1
https://doi.org/10.1158/1078-0432.22440960.v1
Autor:
Michael Tacke, Werner Zolg, Hanno Langen, Wolfgang Rösch, Siegbert Rossol, Gerhard Rohr, Thomas Henkel, Josef Rüschoff, Heinz Bodenmüller, Johann Karl, Herbert Andres, Michael Pfeffer, Bernd Schneidinger, Alfred M. Engel, Peter Berndt, Marie-Luise Hagmann, Stefan Palme, Wolfgang Rollinger, Markus Roeßler
Purpose: The goal of this study was to identify and validate novel serum markers of human colorectal cancer as potential candidates for noninvasive detection of early colorectal neoplasm.Experimental Design: Employing two-dimensional gel electrophore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5868f2ca17fc81b9ebe6479f539f2940
https://doi.org/10.1158/1078-0432.c.6518169
https://doi.org/10.1158/1078-0432.c.6518169
Autor:
Petra, Kiszel, Sonja, Fiesel, Susanne, Voit, Beate, Waechtler, Thomas, Meier, Tobias, Oelschlaegel, Michael, Schraeml, Alfred M, Engel
Publikováno v:
Biotechnology progress. 35(3)
Transient gene expression (TGE) in HEK293 cells was optimized by Vink et al. by co-expression of human cell cycle inhibitors p21
Autor:
Alfred M Engel, David G. Lowe
Publikováno v:
FEBS Letters. (2):169-172
The hormone binding site of rat and human natriuretic peptide clearance receptor (NPR-C), a single transmembrane receptor, has been further refined by mutagenesis. In addition to residue 188 (rat Ala, human Ile), which completely inverts the pharmaco