Evidence map›Paper›PMID 23532366›Full record

ArticleAdvanced functional materials2011

A biologically active surface enzyme assembly that attenuates thrombus formation.

Zheng Qu, Sharmila Muthukrishnan, Murali K Urlam, Carolyn A Haller, Sumanas W Jordan, Vivek A Kumar, Ulla M Marzec, Yaseen Elkasabi, Joerg Lahann, Stephen R Hanson and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Advanced functional materials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. 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

11 authors at 6 institutions in 1 country.

Zheng QuDepartments of Biomedical Engineering and Surgery, Georgia Institute of Technology and Emory University Atlanta, GA 30322 (USA).
Sharmila Muthukrishnan
Murali K Urlam
Carolyn A Haller
Sumanas W Jordan
Vivek A Kumar
Ulla M Marzec
Yaseen Elkasabi
Joerg Lahann
Stephen R Hanson
Elliot L Chaikof
Emory University · USOregon National Primate Research Center · USUniversity of Michigan–Ann Arbor · USBeth Israel Deaconess Medical Center · USGeorgia Institute of Technology · USHarvard University Press · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
MEMBRANE-MIMETIC ASSEMBLIES FOR ENDOTHELIAL MIGRATIONR01HL056819 · NHLBI · EMORY UNIVERSITY · PI CHAIKOF, ELLIOT · 1998 to 2016
$5.2M
Molecularly Engineered Blockade of Islet Induced Inflammatory ResponsesR01DK069275 · NIDDK · EMORY UNIVERSITY · PI CHAIKOF, ELLIOT · 2004 to 2013
$3.2M
Site-Specific Therapies To Prevent Intimal HyperplasiaR01HL106018 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CHAIKOF, ELLIOT · 2011 to 2014
$1.6M
NHLBI NIH HHS R01 HL056819NHLBI NIH HHS R01 HL106018NIDCR NIH HHS T32 DE007057NIDDK NIH HHS R01 DK069275NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

Activation of hemostatic pathways by blood-contacting materials remains a major hurdle in the development of clinically durable artificial organs and implantable devices. We postulate that surface-induced thrombosis may be attenuated by the reconstitution onto blood contacting surfaces of bioactive enzymes that regulate the production of thrombin, a central mediator of both clotting and platelet activation cascades. Thrombomodulin (TM), a transmembrane protein expressed by endothelial cells, is an established negative regulator of thrombin generation in the circulatory system. Traditional techniques to covalently immobilize enzymes on solid supports may modify residues contained within or near the catalytic site, thus reducing the bioactivity of surface enzyme assemblies. In this report, we present a molecular engineering and bioorthogonal chemistry approach to site-specifically immobilize a biologically active recombinant human TM fragment onto the luminal surface of small diameter prosthetic vascular grafts. Bioactivity and biostability of TM modified grafts is confirmed

Indexed as

Biomedical applicationsblood compatibilityStaudinger Ligationthrombosisvascular graft

Identifiers

PMID23532366
PMCPMC3606904
OpenAlexW2134129724

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.