Evidence map›Paper›PMID 28381645›Full record

ArticleThe Biochemical journal2017

Effect of position-specific single-point mutations and biophysical characterization of amyloidogenic peptide fragments identified from lattice corneal dystrophy patients.

Venkatraman Anandalakshmi, Elavazhagan Murugan, Eunice Goh Tze Leng, Lim Wei Ting, Shyam S Chaurasia, Toshio Yamazaki, Toshio Nagashima, Benjamin Lawrence George, Gary Swee Lim Peh, Konstantin Pervushin and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Molecular mechanisms of amyloid disaggregation.Journal of advanced research · 2022
    Review
  6. Article
  7. Article
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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

12 authors at 3 institutions in 1 country.

Venkatraman AnandalakshmiSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Elavazhagan MuruganSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Eunice Goh Tze LengSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Lim Wei TingSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Shyam S ChaurasiaSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Toshio YamazakiRIKEN Centre for Life Science Technologies, Kanagawa 230-0045, Japan.
Toshio NagashimaRIKEN Centre for Life Science Technologies, Kanagawa 230-0045, Japan.
Benjamin Lawrence GeorgeSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Gary Swee Lim PehSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore.
Konstantin PervushinSchool of Biological Sciences, Nanyang Technological University, Singapore 637551 jodmehta@gmail.com lakshminus@gmail.com kpervushin@ntu.edu.sg.
Rajamani LakshminarayananSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore jodmehta@gmail.com lakshminus@gmail.com kpervushin@ntu.edu.sg.
Jodhbir S MehtaSingapore Eye Research Institute, The Academia, 20 College Road, Discovery Tower, Singapore jodmehta@gmail.com lakshminus@gmail.com kpervushin@ntu.edu.sg.
Singapore Eye Research Institute · SGNanyang Technological University · SGDuke-NUS Medical School · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Corneal stromal dystrophies are a group of genetic disorders that may be caused by mutations in the transforming growth factor β-induced (

Indexed as

Point MutationUp-RegulationAmino Acid SubstitutionAmyloidAmyloidogenic ProteinsCells, CulturedChromatography, High Pressure LiquidCircular DichroismCorneaCorneal Dystrophies, HereditaryEye ProteinsHumansKineticsMicroscopy, Electron, TransmissionNuclear Magnetic Resonance, BiomolecularPeptide FragmentsAmyloidAmyloidogenic ProteinsEye ProteinsPeptide FragmentsTGFB1 protein, humanTGFBI protein (611-642), humanTransforming Growth Factor betaTransforming Growth Factor beta1amino acid substitutionamyloidcorneal dystrophyprotein aggregationTGFBIpβ-sheet propensity

Identifiers

PMID28381645
PMCPMC5632800
OpenAlexW2605118158

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.