Evidence map›Paper›PMID 36144015›Full record

ArticleMicromachines2022

Scalable Additive Construction of Arrayed Microstructures with Encoded Properties for Bioimaging.

Matthew DiSalvo, Belén Cortés-Llanos, Cody A LaBelle, David M Murdoch, Nancy L Allbritton

Abstract read
In one paragraph

Article in Micromachines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Matthew DiSalvoMicrosystems and Nanotechnology Division, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.ORCID 0000-0003-1354-5723
Belén Cortés-LlanosDepartment of Bioengineering, University of Washington, Seattle, WA 98105, USA.ORCID 0000-0002-8069-4908
Cody A LaBelleDepartment of Bioengineering, University of Washington, Seattle, WA 98105, USA.ORCID 0000-0002-0947-6545
David M MurdochDepartment of Medicine, Duke University Medical Center, Durham, NC 27705, USA.
Nancy L AllbrittonDepartment of Bioengineering, University of Washington, Seattle, WA 98105, USA.ORCID 0000-0002-9242-768X

Funding

MICROFABRICATED INSTRUMENTATION TO MEASURE SPHINGOLIPID SIGNALING IN HUMAN ACUTE MYELOID LEUKEMIAR01CA233811 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ALLBRITTON, NANCY L., ARMISTEAD, PAUL MICHAEL · 2019 to 2023
$3.1M
PROFILING SIGNALING ACTIVITY AND GENE EXPRESSION IN SINGLE, PANCREATIC ADENOCARCINOMA CELLS USING CE-RNA-SEQR01CA224763 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ALLBRITTON, NANCY L., LAWRENCE, DAVID S. · 2018 to 2022
$2.9M
Magnetically directed single cell transcriptome analysis in HIV latencyR01GM123542 · NIGMS · DUKE UNIVERSITY · PI MURDOCH, DAVID MARTIN · 2016 to 2018
$1.7M
Magnetically directed single cell transcriptome analysis in HIV latencyR01AI150465 · NIAID · DUKE UNIVERSITY · PI MURDOCH, DAVID MARTIN · 2019 to 2020
$1.1M
NCI NIH HHS CA224763NCI NIH HHS CA233811NCI NIH HHS R01 CA224763NCI NIH HHS R01 CA233811NIAID NIH HHS R01 AI150465NIGMS NIH HHS GM123542NIGMS NIH HHS R01 GM123542
6 · The paper itself

Abstract

Microarrays are essential components of analytical instruments. The elements of microarrays may be imbued with additional functionalities and encodings using composite materials and structures, but traditional microfabrication methods present substantial barriers to fabrication, design, and scalability. In this work, a tool-free technique was reported to additively batch-construct micromolded, composite, and arrayed microstructures. The method required only a compatible carrier fluid to deposit a material onto a substrate with some topography. Permutations of this basic fabrication approach were leveraged to gain control over the volumes and positions of deposited materials within the microstructures. As a proof of concept, cell micro-carrier arrays were constructed to demonstrate a range of designs, compositions, functionalities, and applications for composite microstructures. This approach is envisioned to enable the fabrication of complex composite biological and synthetic microelements for biosensing, cellular analysis, and biochemical screening.

Indexed as

barcodingbioimagingmicroarray analysismicrofabricationsingle-cell analysis

Identifiers

PMID36144015
PMCPMC9500771

What OpenQuestion holds

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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.