Evidence map›Paper›PMID 24701393›Full record

ArticleCurrent opinion in chemical engineering2013

Advances in microfluidic cell separation and manipulation.

Emily L Jackson, Hang Lu

Abstract read
In one paragraph

Article in Current opinion in chemical engineering, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  12. Exosomal RNAs: Novel Potential Biomarkers for Diseases-A Review.International journal of molecular sciences · 2022
    Review
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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

2 authors.

Emily L JacksonSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Dr. NW, Atlanta, GA 30332-0100, USA.
Hang LuSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Dr. NW, Atlanta, GA 30332-0100, USA.

Funding

Quantitative microscopy-based rapid phenotyping and screeningR01GM088333 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2011 to 2018
$2.3M
Spatiotemporal control of reactive oxygen species in T cellsR01AI088023 · NIAID · GEORGIA INSTITUTE OF TECHNOLOGY · PI KEMP, MELISSA LAMBETH · 2011 to 2014
$1.4M
Sources, transmission and effects of transcriptional noise in C. elegans agingR01AG035317 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2009 to 2011
$837k
HIGH-THROUGHPUT HIGH-CONTENT PLATFORM FOR IMAGE-BASED SCREENSR21EB012803 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI LU, HANG · 2010 to 2011
$399k
NIAID NIH HHS R01 AI088023NIA NIH HHS R01 AG035317NIBIB NIH HHS R21 EB012803NIGMS NIH HHS R01 GM088333
6 · The paper itself

Abstract

Cellular separations are required in many contexts in biochemical and biomedical applications for the identification, isolation, and analysis of phenotypes or samples of interest. Microfluidics is uniquely suited for handling biological samples, and emerging technologies have become increasingly accessible tools for researchers and clinicians. Here, we review advances in the last few years in techniques for microfluidic cell separation and manipulation. Applications such as high-throughput cell and organism phenotypic screening, purification of heterogeneous stem cell populations, separation of blood components, and isolation of rare cells in patients highlight some of the areas in which these technologies show great potential. Continued advances in separation mechanisms and understanding of cellular systems will yield further improvements in the throughput, resolution, and robustness of techniques.

Identifiers

PMID24701393
PMCPMC3970816

What OpenQuestion holds

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Registered trials

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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.