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Computational and modeling approaches to understand the impact of the Fabry's disease causing mutation (D92Y) on the interaction with pharmacological chaperone 1-deoxygalactonojirimycin (DGJ).
Thirumal Kumar D, Judith E, Priyadharshini Christy J, Siva R, Tayubi IA, Chakraborty C, George Priya Doss C, Zayed H. Thirumal Kumar D, et al. Among authors: tayubi ia. Adv Protein Chem Struct Biol. 2019;114:341-407. doi: 10.1016/bs.apcsb.2018.10.009. Epub 2018 Dec 18. Adv Protein Chem Struct Biol. 2019. PMID: 30635085 Review.
Understanding the structure-function relationship of HPRT1 missense mutations in association with Lesch-Nyhan disease and HPRT1-related gout by in silico mutational analysis.
Agrahari AK, Krishna Priya M, Praveen Kumar M, Tayubi IA, Siva R, Prabhu Christopher B, George Priya Doss C, Zayed H. Agrahari AK, et al. Among authors: tayubi ia. Comput Biol Med. 2019 Apr;107:161-171. doi: 10.1016/j.compbiomed.2019.02.014. Epub 2019 Feb 23. Comput Biol Med. 2019. PMID: 30831305
Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease.
Sundarrajan S, Venkatesan A, Kumar S U, Gopikrishnan M, Tayubi IA, Aditya M, Siddaiah GB, George Priya Doss C, Zayed H. Sundarrajan S, et al. Among authors: tayubi ia. Metab Brain Dis. 2023 Aug;38(6):2025-2036. doi: 10.1007/s11011-023-01221-7. Epub 2023 May 10. Metab Brain Dis. 2023. PMID: 37162726 Free PMC article.
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