Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Markus Stöcher"'
Autor:
Markus Stöcher, Jörg Berg
Publikováno v:
BioTechniques, Vol 36, Iss 3, Pp 480-482 (2004)
Externí odkaz:
https://doaj.org/article/87b7c1a7001a4af1860dbaaa94b52e4b
Autor:
Christoph Heyder, Zlatko Trajanoski, Richard Greil, Daniela Asslaber, Christine Papak, Olaf Merkel, Claudia Holler, Inge Tinhofer, Andreas Prokesch, Markus Stöcher, Frank Hamacher, Marcel Scheideler
Publikováno v:
Journal of Molecular Medicine. 86:541-552
In the last decade, arsenic trioxide (As2O3) has been used very successfully to treat acute promyelocytic leukaemia (APL). Much less is known about the effectiveness of As2O3 in other neoplastic disorders. In this paper, we report that after 18 h in
Autor:
Markus Stöcher, Herbert Stekel, Gerd Bodlaj, Rainer Hubmann, Georg Biesenbach, Peter Hufnagl, Jörg Berg
Publikováno v:
Clinical Chemistry. 52:148-151
Background: Hypolactasia and lactose intolerance are common conditions worldwide. Hypolactasia seems to be strongly correlated with genotype C/C of the genetic variant C→T−13910 upstream of the lactase phlorizin hydrolase (LPH) gene. We developed
Autor:
Jörg Berg, Markus Stöcher
Publikováno v:
Clinical Chemistry
Real-time PCR assays are widely used for the detection and quantification of pathogen-derived nucleic acids in clinical samples (1)(2)(3). Because clinical specimens contain PCR-inhibitory moieties that are not always reliably removed during nucleic
Publikováno v:
Journal of Clinical Virology. 29:171-178
Background: Herpes viruses represent important causes of morbidity and mortality especially in immuno-compromised patients. To assist in rapid diagnosis real-time PCR assays have been developed for the detection of herpes virus DNA in patient specime
Autor:
Elizabeth Valentine-Thon, Victoria Leb, Harald H. Kessler, Markus Stöcher, Jörg Berg, Herbert Stekel, Gabriele Hölzl
Publikováno v:
Journal of Clinical Microbiology. 42:585-590
We report on the development of a fully automated real-time PCR assay for the quantitative detection of hepatitis B virus (HBV) DNA in plasma with EDTA (EDTA plasma). The MagNA Pure LC instrument was used for automated DNA purification and automated
Publikováno v:
Journal of Virological Methods. 108:1-8
Real-time polymerase chain reaction (PCR) assays allow convenient detection and quantitation of virus-derived nucleic acids in clinical specimens. When specimens are assayed for the presence of virus-derived nucleic acids against external standards,
Autor:
Markus Stöcher, Victoria Leb, Gabriele Halwachs-Baumann, Olfert Landt, Michael Bozic, Herbert Stekel, Harald H. Kessler, Jörg Berg
Publikováno v:
Journal of Clinical Virology. 26:85-93
Background: Human herpes viruses cause a spectrum of diseases that are usually self-limiting but can be reactive during immuno-suppression and may then lead to severe or even life-threatening diseases. The LightCycler technology allows rapid polymera
Publikováno v:
Journal of Clinical Virology. 25:47-53
Background: The real-time PCR technology allows convenient detection and quantification of virus derived DNA. This approach is used in many PCR based assays in clinical laboratories. Detection and quantification of virus derived DNA is usually perfor
Autor:
Jörg Berg, Markus Stöcher
Publikováno v:
Journal of Clinical Microbiology. 40:4547-4553
The development of a novel normalized quantitative competitive real-time PCR on the LightCycler instrument (NQC-LC-PCR) and its application to the quantification of cytomegalovirus (CMV) DNA in clinical samples are described. A heterologous competito