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Martin Plchút

dblp:31/4248 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2007
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › systems biology › cellular dynamics
apoptosis modeling
0.112007
APOPTO-CELL - a simulation tool and interactive database for analyzing cellular susceptibility to apoptosis · Bioinform. 2007
Bioinformatics and computational biology › systems biology › biochemical reaction network modeling
biochemical reaction network simulation
0.112007
APOPTO-CELL - a simulation tool and interactive database for analyzing cellular susceptibility to apoptosis · Bioinform. 2007
Bioinformatics and computational biology
systems biology
0.112007
APOPTO-CELL - a simulation tool and interactive database for analyzing cellular susceptibility to apoptosis · Bioinform. 2007

Methods — techniques the papers use, named apart from their topics

ordinary differential equations · 0.1monte carlo simulation · 0.1
YearPublicationVenuePosition
2007 APOPTO-CELL - a simulation tool and interactive database for analyzing cellular susceptibility to apoptosis
abstract
UNLABELLED: We have developed a web service that provides a comprehensive analysis of the susceptibility of cells to undergo apoptosis in response to an activation of the mitochondrial apoptotic pathway. Based on ordinary differential equations, (pre-determined) protein concentrations and release kinetics of mitochondrial pro-apoptotic factors, a network of 52 reactions and 19 reaction partners can be employed as a tool to display temporal protein profiles, to identify key regulatory proteins and to determine critical threshold concentrations required for the execution of apoptosis in HeLa cancer cells or other cell types. The web service also provides an interactive database function for the deposition of cell-type-specific quantitative data. In addition, the web service provides an output that can be compared directly to experimental results obtained from real-time single-cell experiments, making this a widely applicable systems biology tool for apoptosis and cancer researchers. AVAILABILITY: http://systemsbiology.rcsi.ie/apopto-cell.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Heinrich J. Huber, Markus Rehm 0001, Martin Plchút, Heiko Duessmann, Jochen H. M. Prehn
Bioinform.3