Evidence map›Paper›PMID 30206180›Full record

ArticleMolecular & cellular proteomics : MCP2018

Knockout of the Hmt1p Arginine Methyltransferase in

Samantha Z Chia, Yu-Wen Lai, Daniel Yagoub, Sophie Lev, Joshua J Hamey, Chi Nam Ignatius Pang, Desmarini Desmarini, Zhiliang Chen, Julianne T Djordjevic, Melissa A Erce and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2018. 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
0.4field-weighted citation impact, top 39% 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, 14 citations in OpenAlex.

  1. LC-MS profiling ofbioRxiv : the preprint server for biology · 2026
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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 2 institutions in 1 country.

Samantha Z ChiaSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Yu-Wen LaiSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Daniel YagoubSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Sophie LevCentre for Infectious Diseases and Microbiology, Westmead Millennium Institute and Sydney Medical School, University of Sydney at Westmead Hospital, Westmead, New South Wales, Australia.
Joshua J HameySystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Chi Nam Ignatius PangSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Desmarini DesmariniCentre for Infectious Diseases and Microbiology, Westmead Millennium Institute and Sydney Medical School, University of Sydney at Westmead Hospital, Westmead, New South Wales, Australia.
Zhiliang ChenSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Julianne T DjordjevicCentre for Infectious Diseases and Microbiology, Westmead Millennium Institute and Sydney Medical School, University of Sydney at Westmead Hospital, Westmead, New South Wales, Australia.
Melissa A ErceSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Gene Hart-SmithSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Marc R WilkinsSystems Biology Initiative, School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia. Electronic address: m.wilkins@unsw.edu.au.
UNSW Sydney · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hmt1p is the predominant arginine methyltransferase in

Indexed as

Acid PhosphataseArginineDNA-Binding ProteinsGene Expression ProfilingGene Expression RegulationGene Knockout TechniquesHomeostasisMethylationMicroscopy, FluorescencePhosphatesProtein-Arginine N-MethyltransferasesProteomeRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTandem Mass SpectrometryAcid PhosphataseArginineDNA-Binding ProteinsHMT1 protein, S cerevisiaePHO4 protein, S cerevisiaePhosphatesProtein-Arginine N-MethyltransferasesProteomeRepressor ProteinsSaccharomyces cerevisiae ProteinsTranscription FactorsFluorescenceHmt1pKnockoutsMethylationMolecular biologyPho4pPHO regulonPhosphate regulationRNA SEQSILACYeast

Identifiers

PMID30206180
PMCPMC6283299
OpenAlexW2892334737

What Socratic holds

Textmetadata
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 Socratic graph.