Evidence map›Paper›PMID 34297307›Full record

ArticleImmunologic research2021

A graph centrality-based approach for candidate gene prediction for type 1 diabetes.

N B Thummadi, E Vishnu, E V Subbiah, P Manimaran

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Article in Immunologic research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

N B ThummadiDepartment of Animal Biology, University of Hyderabad, Gachibowli, Hyderabad, 500046, India.
E VishnuSchool of Physics, University of Hyderabad, Gachibowli, Hyderabad, 500046, Telangana, India.
E V SubbiahDepartment of Sports Biosciences, Central University of Rajasthan, Kishangarh, Ajmer, 305817, India.
P ManimaranSchool of Physics, University of Hyderabad, Gachibowli, Hyderabad, 500046, Telangana, India. pa.manimaran@gmail.com.ORCID 0000-0003-0717-7573
University of Hyderabad · INCentral University of Rajasthan · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 diabetes mellitus (T1DM) or insulin-dependent diabetes is an autoimmune disease that may pose life-threatening situations to individuals. In most cases, cytotoxic T lymphocytes (CTLs) promotes killing of islets of Langerhans in the pancreas, which harbour insulin-producing beta cells. The trigger for autoimmune attack is still unclear; therefore, identifying and targeting candidate genes are imperative to hinder its deleterious effects. In the present study, we focused on identification of new candidate genes for T1DM. For our study, we exclusively selected immune-related genes as they play a crucial role in T1DM. We constructed and analysed a human immunome signalling network (directed network) to identify the new candidate genes through various graph centrality measures combining with Gene Ontology (GO). As a result, we identified 4 new candidate genes which may act as potential drug targets for T1DM. We further validated for their disease relevance through literature survey and pathway analysis and found that 3 out of 4 predicted genes mirrored their well-established roles as potential targets for T1DM.

Indexed as

Computer GraphicsGenetic Predisposition to DiseaseUser-Computer InterfaceAlgorithmsBiomarkersComputational BiologyDatabases, GeneticDiabetes Mellitus, Type 1Gene Expression RegulationGenetic Association StudiesGenome-Wide Association StudyHumansPrognosisSignal TransductionBiomarkersAutoimmune diseaseCandidate geneGene OntologyGraph centralityProtein interaction network

Identifiers

PMID34297307
OpenAlexW3184702942

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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.