Evidence map›Paper›PMID 31069329›Full record

ArticleAPL bioengineering2018

Extracellular matrix alignment dictates the organization of focal adhesions and directs uniaxial cell migration.

William Y Wang, Alexander T Pearson, Matthew L Kutys, Colin K Choi, Michele A Wozniak, Brendon M Baker, Christopher S Chen

Open access · goldAbstract read
In one paragraph

Article in APL bioengineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
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

71 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
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  11. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    Review
  12. Review
  13. Article
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  15. Article
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  18. Article
  19. Article
  20. FAK Differentially Mechanoregulates Cell Migration During Wound Closure.bioRxiv : the preprint server for biology · 2025
    Article

11 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 1 country.

William Y WangDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.ORCID 0000-0001-9669-4841
Alexander T PearsonSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois 60637, USA.ORCID 0000-0003-2801-7456
Matthew L Kutys
Colin K Choi
Michele A WozniakDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Brendon M BakerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, USA.
Christopher S Chen
Boston University · USUniversity of Michigan · USUniversity of Chicago · USUniversity of Pennsylvania · US

Funding

A reasoned approach to combination therapy development in head and neck cancerK08DE026500 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PEARSON, ALEXANDER THOMAS · 2016 to 2020
$800k
Non-canonical Notch1 regulation of proliferation and adherens junctions in breast cancerK99CA226366 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KUTYS, MATTHEW L · 2018 to 2019
$323k
NCI NIH HHS K99 CA226366NIDCR NIH HHS K08 DE026500
6 · The paper itself

Abstract

Physical features of the extracellular matrix (ECM) heavily influence cell migration strategies and efficiency. Migration in and on fibrous ECMs is of significant physiologic importance, but limitations in the ability to experimentally define the diameter, density, and alignment of native ECMs

Identifiers

PMID31069329
PMCPMC6481732
OpenAlexW2905604137

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.