Evidence map›Paper›PMID 39221109›Full record

ArticleMatter2024

Rapid Tissue Perfusion Using Sacrificial Percolation of Anisotropic Networks.

Alex Lammers, Heng-Hua Hsu, Subramanian Sundaram, Keith A Gagnon, Sudong Kim, Joshua H Lee, Yi-Chung Tung, Jeroen Eyckmans, Christopher S Chen

Abstract read
In one paragraph

Article in Matter, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. 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

9 authors.

Alex LammersThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Heng-Hua HsuResearch Center for Applied Sciences, Academia Sinica, Taipei 11529, Taiwan.
Subramanian SundaramThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Keith A GagnonThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Sudong KimThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Joshua H LeeThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Yi-Chung TungResearch Center for Applied Sciences, Academia Sinica, Taipei 11529, Taiwan.
Jeroen EyckmansThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Christopher S ChenThe Biological Design Center and Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.

Funding

BIOLOGY OF THE LUNG--MULTIDISCIPLINARY PROGRAMT32HL007035 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Darrell N. Kotton, JOSEPH P MIZGERD · 1985 to 2026
$24.3M
REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
TRAINING PROGRAM IN QUANTITATIVE BIOLOGY AND PHYSIOLOGYT32GM008764 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI WHITE, JOHN A. · 2001 to 2021
$5.9M
Synthetic vascularization and regeneration in engineered tissuesR01EB033821 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SANGEETA N. BHATIA, CHRISTOPHER S CHEN · 2023 to 2026
$2.2M
Elucidating Mechanisms for Rapid Vascularization by Modeling Vascular Islands in Early EmbryogenesisF31HL156517 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI LAMMERS, ALEX · 2021 to 2023
$117k
NHLBI NIH HHS F31 HL156517NHLBI NIH HHS T32 HL007035NIBIB NIH HHS R01 EB000262NIBIB NIH HHS R01 EB033821NIGMS NIH HHS T32 GM008764
6 · The paper itself

Abstract

Tissue engineering has long sought to rapidly generate perfusable vascularized tissues with vessel sizes spanning those seen in humans. Current techniques such as biological 3D printing (top-down) and cellular self-assembly (bottom-up) are resource intensive and have not overcome the inherent tradeoff between vessel resolution and assembly time, limiting their utility and scalability for engineering tissues. We present a flexible and scalable technique termed SPAN -

Indexed as

anisotropic percolationbiofabricationmicrofluidicssacrificial castingself-assemblytissue engineeringvascular engineeringvessel networkvolumetric subtractive manufacturing

Identifiers

PMID39221109
PMCPMC11360881

What OpenQuestion holds

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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.