Evidence map›Paper›PMID 20012047›Full record

ArticleJournal of mathematical biology2010

Stochastic modelling of biased cell migration and collagen matrix modification.

Andreas Groh, Alfred K Louis

Abstract read
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In one paragraph

Article in Journal of mathematical biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Mathematical modelling of angiogenesis using continuous cell-based models.Biomechanics and modeling in mechanobiology · 2016
    Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Andreas GrohFakultät für Mathematik und Informatik, Postfach 151150, 66041, Saarbrücken, Germany. groh@num.uni-sb.de
Alfred K Louis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix dynamics plays a crucial role in several physiological and pathological processes. In this paper we develop a model framework, which describes the temporal fibre network evolution depending on the influence of migrating fibroblasts. The cells are regarded as discrete objects in the plane, whose velocities are determined by a generalised Langevin equation. For its solution we verify existence and uniqueness. The courses of the trajectories are affected by two external impulses, chemotaxis and contact guidance, respectively. The extracellular matrix is described by a continuous vector field which contains both information on density and orientation of the fibrous material. Modelling dynamic interaction between the discrete and the continuum variables is an essential point of this paper. In particular, the smoothing of the fluctuating paths plays a key role. Besides a detailed description of the formulated equations, we also supply the condensed pseudo code of the algorithm. We investigate several examples and present results both from artificial and real data.

Indexed as

Models, BiologicalAlgorithmsCarcinoma, Squamous CellCell AdhesionCell MovementChemotactic FactorsChemotaxisCollagenComputer SimulationDiffusionExtracellular MatrixFibroblastsHumansLung NeoplasmsNeoplasmsStochastic ProcessesChemotactic FactorsCollagen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.