Evidence map›Paper›PMID 30037463›Full record

ArticleMethods in cell biology2018

Microfluidics for mechanobiology of model organisms.

Anna A Kim, Adam L Nekimken, Sylvia Fechner, Lucy E O'Brien, Beth L Pruitt

Abstract read
In one paragraph

Article in Methods in cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  10. HowGenetics · 2019
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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

5 authors at 3 institutions in 2 countries.

Anna A KimUniversity of California, Santa Barbara, CA, United States; Uppsala University, Uppsala, Sweden; Stanford University, Stanford, CA, United States.
Adam L NekimkenStanford University, Stanford, CA, United States.
Sylvia FechnerStanford University, Stanford, CA, United States.
Lucy E O'BrienStanford University, Stanford, CA, United States.
Beth L PruittUniversity of California, Santa Barbara, CA, United States; Stanford University, Stanford, CA, United States. Electronic address: pruitt@stanford.edu.
Stanford University · USUniversity of California, Santa Barbara · USUppsala University · SE

Funding

Molecular Basis of Sensory Transduction in C. elegansR01NS047715 · NINDS · STANFORD UNIVERSITY · PI GOODMAN, MIRIAM B · 2004 to 2017
$4.9M
Force Clamp Systems for Evaluation of MechanotransductionR01EB006745 · NIBIB · STANFORD UNIVERSITY · PI GOODMAN, MIRIAM B, PRUITT, BETH L · 2007 to 2014
$3.1M
Dynamic Mechanisms of Fate Control during Epithelial Organ RenewalR01GM116000 · NIGMS · STANFORD UNIVERSITY · PI O'BRIEN, LUCY ERIN · 2016 to 2020
$1.6M
Request to purchase replace cryogenic storage equipment to preserve biological reagents.R01NS092099 · NINDS · STANFORD UNIVERSITY · PI GOODMAN, MIRIAM B · 2015 to 2017
$1.1M
Validating engineered hiPSC-derived cardiomyocytes as model cellsR21HL130993 · NHLBI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI PRUITT, BETH L · 2016 to 2017
$434k
Internal Tissue Mechanics and the Sense of Touch in C. elegansF31NS100318 · NINDS · STANFORD UNIVERSITY · PI NEKIMKEN, ADAM · 2017 to 2019
$106k
NHLBI NIH HHS R21 HL130993NIBIB NIH HHS R01 EB006745NIGMS NIH HHS R01 GM116000NINDS NIH HHS F31 NS100318NINDS NIH HHS R01 NS047715NINDS NIH HHS R01 NS092099
6 · The paper itself

Abstract

Mechanical stimuli play a critical role in organ development, tissue homeostasis, and disease. Understanding how mechanical signals are processed in multicellular model systems is critical for connecting cellular processes to tissue- and organism-level responses. However, progress in the field that studies these phenomena, mechanobiology, has been limited by lack of appropriate experimental techniques for applying repeatable mechanical stimuli to intact organs and model organisms. Microfluidic platforms, a subgroup of microsystems that use liquid flow for manipulation of objects, are a promising tool for studying mechanobiology of small model organisms due to their size scale and ease of customization. In this work, we describe design considerations involved in developing a microfluidic device for studying mechanobiology. Then, focusing on worms, fruit flies, and zebrafish, we review current microfluidic platforms for mechanobiology of multicellular model organisms and their tissues and highlight research opportunities in this developing field.

Indexed as

Models, BiologicalAnimalsBiophysicsLab-On-A-Chip DevicesMicrofluidicsC. elegansDrosophilaMechanobiologyMicrofluidicsMulticellular model organismsZebrafish

Identifiers

PMID30037463
PMCPMC6418080
OpenAlexW2883844279

What OpenQuestion holds

Textmetadata
LicenceTDM
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.