Evidence map›Paper›PMID 37153521›Full record

ArticleFrontiers in chemistry2023

Predicting the effects of rare genetic variants on oncogenic signaling pathways: A computational analysis of HRAS protein function.

Sadaqat Ali, Usman Ali, Adeem Qamar, Imran Zafar, Muhammad Yaqoob, Qurat Ul Ain, Summya Rashid, Rohit Sharma, Hiba-Allah Nafidi, Yousef A Bin Jardan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in chemistry, 2023. 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
6.3field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  7. Heliyon · 2023
    Article
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  9. Frontiers in chemistry · 2023
    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 7 institutions in 5 countries.

Sadaqat AliMedical Department, DHQ Hospital Bhawalnagr, Punjab, Pakistan.
Usman AliBasic Health Unit, Punjab, Pakistan.
Adeem QamarDepartment of Pathology, Sahiwal Medical College Sahiwal, Punjab, Pakistan.
Imran ZafarDepartment of Bioinformatics and Computational Biology, Virtual University of Pakistan, Punjab, Pakistan.
Muhammad YaqoobDepartment of Life Sciences, ARID University-Barani Institute of Sciences Burewala Campus, Punjab, Pakistan.
Qurat Ul AinDepartment of Chemistry, Government College Women University, Faisalabad, Pakistan.
Summya RashidDepartment of Bioinformatics and Computational Biology, Virtual University of Pakistan, Punjab, Pakistan.
Rohit SharmaDepartment of Rasa Shastra and Bhaishajya Kalpana, Faculty of Ayurveda, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.
Hiba-Allah NafidiDepartment of Food Science, Faculty of Agricultural and Food Sciences, Laval University, Quebec City, QC, Canada.
Yousef A Bin JardanDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Mohammed BourhiaLaboratory of Chemistry and Biochemistry, Faculty of Medicine and Pharmacy, Ibn Zohr University, Agadir, Morocco.
Virtual University of Pakistan · PKBanaras Hindu University · INGovernment College Women University Faisalabad · PKKing Saud University · SAPir Mehr Ali Shah Arid Agriculture University · PKUniversité Ibn Zohr · MAUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The HRAS gene plays a crucial role in regulating essential cellular processes for life, and this gene's misregulation is linked to the development of various types of cancers. Nonsynonymous single nucleotide polymorphisms (nsSNPs) within the coding region of HRAS can cause detrimental mutations that disrupt wild-type protein function. In the current investigation, we have employed

Indexed as

cancergenetic variantsHRASmutationsnsSNPoncogenic signaling pathwaysSNPs

Identifiers

PMID37153521
PMCPMC10160440
OpenAlexW4366690497

What Socratic holds

Textmetadata
LicenceCC BY
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.