Evidence map›Paper›PMID 29318563›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2018

Generation of Highly Selective MMP Antibody Inhibitors.

Dong Hyun Nam, Xin Ge

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Generation of Protease Inhibitory Antibodies by Functional In Vivo Selection.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Inhibition of MMPs and ADAM/ADAMTS.Biochemical pharmacology · 2019
    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

2 authors.

Dong Hyun NamDepartment of Chemical and Environmental Engineering, University of California, Riverside, CA, USA.
Xin GeDepartment of Chemical and Environmental Engineering, University of California, Riverside, CA, USA. xge@engr.ucr.edu.

Funding

Structure-based design of camel-like human selective mAbs against MMPs in diseaseR01GM115672 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI GE, XIN · 2016 to 2020
$1.5M
NIGMS NIH HHS R01 GM115672
6 · The paper itself

Abstract

Inhibiting individual MMPs of biomedical importance with high selectivity is critical for both fundamental research and therapy development. Here we describe the methods for discovery of inhibitory monoclonal antibodies from synthetic human antibody phage display libraries carrying convex paratopes encoded by long complementarity-determining region (CDR)-H3 segments. We demonstrate the application of this technique for isolation of highly specific and potent antibody inhibitors of human MMP-14.

Indexed as

Peptide LibraryAntibodies, MonoclonalBinding Sites, AntibodyComplementarity Determining RegionsDrug DiscoveryImmunoglobulin Fab FragmentsMatrix Metalloproteinase 14Matrix Metalloproteinase InhibitorsAntibodies, MonoclonalComplementarity Determining RegionsImmunoglobulin Fab FragmentsMatrix Metalloproteinase 14Matrix Metalloproteinase InhibitorsMMP14 protein, humanPeptide LibraryConvex paratopeInhibitory antibodyLong CDRSynthetic library

Identifiers

PMID29318563
PMCPMC5901970

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.