C. George Priya Doss

Orcid: 0000-0002-5971-8290

According to our database1, C. George Priya Doss authored at least 16 papers between 2008 and 2023.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

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Bibliography

2023
<i>In silico</i> analysis revealed the potential circRNA-miRNA-mRNA regulative network of non-small cell lung cancer (NSCLC).
Comput. Biol. Medicine, 2023

2022
Towards computational solutions for precision medicine based big data healthcare system using deep learning models: A review.
Comput. Biol. Medicine, 2022

Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes.
Comput. Biol. Medicine, 2022

2021
Computational investigation to identify potent inhibitors of the GTPase-Kirsten RAt sarcoma virus (K-Ras) mutants G12C and G12D.
Comput. Biol. Medicine, 2021

Residue interaction networks of K-Ras protein with water molecules identifies the potential role of switch II and P-loop.
Comput. Biol. Medicine, 2021

Computational validation of <i>ABCB1</i> gene polymorphism and its effect on tacrolimus dose concentration/levels in renal transplant individuals of South India.
Comput. Biol. Medicine, 2021

Effective utilisation of influence maximization technique for the identification of significant nodes in breast cancer gene networks.
Comput. Biol. Medicine, 2021

Investigation of nonsynonymous mutations in the spike protein of SARS-CoV-2 and its interaction with the ACE2 receptor by molecular docking and MM/GBSA approach.
Comput. Biol. Medicine, 2021

2020
An extensive computational approach to analyze and characterize the functional mutations in the galactose-1-phosphate uridyl transferase (GALT) protein responsible for classical galactosemia.
Comput. Biol. Medicine, 2020

2019
Exploring the codon patterns between <i>CCD</i> and <i>NCED</i> genes among different plant species.
Comput. Biol. Medicine, 2019

A computational approach for investigating the mutational landscape of RAC-alpha serine/threonine-protein kinase (AKT1) and screening inhibitors against the oncogenic E17K mutation causing breast cancer.
Comput. Biol. Medicine, 2019

Understanding the structure-function relationship of <i>HPRT1</i> missense mutations in association with Lesch-Nyhan disease and HPRT1-related gout by in silico mutational analysis.
Comput. Biol. Medicine, 2019

2014
Impact of Single amino acid Polymorphisms in Protein-Protein interactions in tumorigenic cluster A and cluster B of VHL: Computational molecular dynamics.
Proceedings of the International Work-Conference on Bioinformatics and Biomedical Engineering, 2014

2013
In silico analysis of detrimental mutations in ADD domain of chromatin remodeling protein ATRX that cause ATR-X syndrome: X-linked disorder.
Netw. Model. Anal. Health Informatics Bioinform., 2013

2008
Identification and structural comparison of deleterious mutations in nsSNPs of ABL1 gene in chronic myeloid leukemia: A bio-informatics study.
J. Biomed. Informatics, 2008

Analysis of binding residues between scorpion neurotoxins and D2 dopamine receptor: A computational docking study.
Comput. Biol. Medicine, 2008


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