Evidence map›Paper›PMID 24567663›Full record

ArticleJournal of membrane science2014

Microfabrication of High-Resolution Porous Membranes for Cell Culture.

Monica Y Kim, David Jiang Li, Long K Pham, Brandon G Wong, Elliot E Hui

Abstract read
In one paragraph

Article in Journal of membrane science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Robust and Gradient Thickness Porous Membranes forAdvanced materials technologies · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Frontiers in medical technology · 2020
    Review
  20. 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

5 authors.

Monica Y KimDepartment of Biomedical Engineering, University of California, Irvine 3120 Natural Sciences II, Irvine, CA 92697-2715 +1-949-824-8723 (O) | +1-949-824-1727 (F) |
David Jiang LiDepartment of Biomedical Engineering, University of California, Irvine 3120 Natural Sciences II, Irvine, CA 92697-2715 +1-949-824-8723 (O) | +1-949-824-1727 (F) |
Long K PhamDepartment of Biomedical Engineering, University of California, Irvine 3120 Natural Sciences II, Irvine, CA 92697-2715 +1-949-824-8723 (O) | +1-949-824-1727 (F) |
Brandon G WongDepartment of Biomedical Engineering, University of California, Irvine 3120 Natural Sciences II, Irvine, CA 92697-2715 +1-949-824-8723 (O) | +1-949-824-1727 (F) |
Elliot E HuiDepartment of Biomedical Engineering, University of California, Irvine 3120 Natural Sciences II, Irvine, CA 92697-2715 +1-949-824-8723 (O) | +1-949-824-1727 (F) |

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Uncover Strategies Used By Biological SystemsP50GM076516 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI NIE, QING · 2007 to 2016
$25.1M
YEAST RIBOSOMAL STALK COMPOSITION IN VIVO BY TWO-PHOTON FCS AND PCH ANALYSISP41RR003155 · NCRR · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI GRATTON, ENRICO · 1986 to 2011
$14.9M
TRD4: Phasor analysisP41GM103540 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GRATTON, ENRICO · 2012 to 2020
$12.5M
NCI NIH HHS P30 CA062203NCRR NIH HHS P41 RR003155NIGMS NIH HHS P41 GM103540NIGMS NIH HHS P50 GM076516
6 · The paper itself

Abstract

Microporous membranes are widely utilized in cell biology to study cell-cell signaling and cell migration. However, the thickness and low porosity of commercial track-etched membranes limit the quality of cell imaging and the degree of cell-cell contact that can be achieved on such devices. We employ photolithography-based microfabrication to achieve porous membranes with pore diameter as small as 0.9 μm, up to 40% porosity, and less than 5% variation in pore size. Through the use of a soap release layer, membranes as thin as 1 μm can be achieved. The thin membranes minimally disrupt contrast enhancement optics, thus allowing good quality imaging of unlabeled cells under white light, unlike commercial membranes. In addition, the polymer membrane materials display low autofluorescence even after patterning, facilitating high quality fluorescence microscopy. Finally, confocal imaging suggests that substantial cell-cell contact is possible through the pores of these thin membranes. This membrane technology can enhance existing uses of porous membranes in cell biology as well as enable new types of experiments.

Indexed as

cell biologymicroporous

Identifiers

PMID24567663
PMCPMC3931465

What OpenQuestion holds

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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.