194 related articles for article (PubMed ID: 38773180)
1. In silico functional, structural and pathogenicity analysis of missense single nucleotide polymorphisms in human MCM6 gene.
Kamal MM; Mia MS; Faruque MO; Rabby MG; Islam MN; Talukder MEK; Wani TA; Rahman MA; Hasan MM
Sci Rep; 2024 May; 14(1):11607. PubMed ID: 38773180
[TBL] [Abstract][Full Text] [Related]
2. Prediction of the most deleterious non-synonymous SNPs in the human IL1B gene: evidence from bioinformatics analyses.
Abuzaid O; Idris AB; Yılmaz S; Idris EB; Idris LB; Hassan MA
BMC Genom Data; 2024 Jun; 25(1):56. PubMed ID: 38858637
[TBL] [Abstract][Full Text] [Related]
3. Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences.
Emadi E; Akhoundi F; Kalantar SM; Emadi-Baygi M
BMC Genet; 2020 Aug; 21(1):94. PubMed ID: 32867672
[TBL] [Abstract][Full Text] [Related]
4. In Silico Analysis of FMR1 Gene Missense SNPs.
Tekcan A
Cell Biochem Biophys; 2016 Jun; 74(2):109-27. PubMed ID: 26880065
[TBL] [Abstract][Full Text] [Related]
5. Computational analysis of sodium-dependent phosphate transporter SLC20A1/PiT1 gene identifies missense variations C573F, and T58A as high-risk deleterious SNPs.
Siva Sankari G; James R; Payva F; Sivaramakrishnan V; Vineeth Kumar TV; Kanchi S; Santhy KS
J Biomol Struct Dyn; 2024 May; 42(8):4072-4086. PubMed ID: 37286379
[TBL] [Abstract][Full Text] [Related]
6. Computational analysis of structural and functional evaluation of the deleterious missense variants in the human
Bouqdayr M; Abbad A; Baba H; Saih A; Wakrim L; Kettani A
J Biomol Struct Dyn; 2023; 41(23):14179-14196. PubMed ID: 36764830
[TBL] [Abstract][Full Text] [Related]
7. Computational identification and analysis of deleterious non-synonymous single nucleotide polymorphisms (nsSNPs) in the human
Kumar R; Jayaraman M; Ramadas K; Chandrasekaran A
J Biomol Struct Dyn; 2024; 42(3):1518-1532. PubMed ID: 37173831
[TBL] [Abstract][Full Text] [Related]
8. In Silico Functional and Structural Analysis of Non-synonymous Single Nucleotide Polymorphisms (nsSNPs) in Human Paired Box 4 Gene.
Kamal MM; Islam MN; Rabby MG; Zahid MA; Hasan MM
Biochem Genet; 2023 Dec; ():. PubMed ID: 38062275
[TBL] [Abstract][Full Text] [Related]
9. Identification of functional SNPs in BARD1 gene and in silico analysis of damaging SNPs: based on data procured from dbSNP database.
Alshatwi AA; Hasan TN; Syed NA; Shafi G; Grace BL
PLoS One; 2012; 7(10):e43939. PubMed ID: 23056176
[TBL] [Abstract][Full Text] [Related]
10. Molecular dynamics simulations and bioinformatics' analysis of deleterious missense single nucleotide polymorphisms in Glyoxalase-1 gene.
Syed NA; Bhatti A; John P
J Biomol Struct Dyn; 2023; 41(23):13707-13717. PubMed ID: 36812296
[TBL] [Abstract][Full Text] [Related]
11. Evolution- and structure-based computational strategy reveals the impact of deleterious missense mutations on MODY 2 (maturity-onset diabetes of the young, type 2).
George DC; Chakraborty C; Haneef SA; Nagasundaram N; Chen L; Zhu H
Theranostics; 2014; 4(4):366-85. PubMed ID: 24578721
[TBL] [Abstract][Full Text] [Related]
12. Functional and Structural Impact of Deleterious Missense Single Nucleotide Polymorphisms in the NR3C1, CYP3A5, and TNF-α Genes: An In Silico Analysis.
Ramayanam NR; Manickam R; Mahalingam VT; Goh KW; Ardianto C; Ganesan P; Ming LC; Ganesan RM
Biomolecules; 2022 Sep; 12(9):. PubMed ID: 36139147
[TBL] [Abstract][Full Text] [Related]
13. Exploring the impact of CYP11A1's missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study.
Redouane S; Harmak H; Elkarhat Z; Charoute H; Malki A; Barakat A; Rouba H
Comput Biol Chem; 2023 Oct; 106():107937. PubMed ID: 37552904
[TBL] [Abstract][Full Text] [Related]
14. Identification and characterization of functional single nucleotide polymorphisms (SNPs) in Axin 1 gene: a molecular dynamics approach.
Khan I; Ansari IA; Singh P; Dass JFP; Khan F
Cell Biochem Biophys; 2018 Jun; 76(1-2):173-185. PubMed ID: 28770488
[TBL] [Abstract][Full Text] [Related]
15. An integrated in silico approach to analyze the involvement of single amino acid polymorphisms in FANCD1/BRCA2-PALB2 and FANCD1/BRCA2-RAD51 complex.
Doss CG; Nagasundaram N
Cell Biochem Biophys; 2014 Nov; 70(2):939-56. PubMed ID: 24817641
[TBL] [Abstract][Full Text] [Related]
16. In silico analysis of non-synonymous single nucleotide polymorphisms in human DAZL gene associated with male infertility.
Nailwal M; Chauhan JB
Syst Biol Reprod Med; 2017 Aug; 63(4):248-258. PubMed ID: 28388287
[TBL] [Abstract][Full Text] [Related]
17. In silico analyses of deleterious missense SNPs of human apolipoprotein E3.
Pires AS; Porto WF; Franco OL; Alencar SA
Sci Rep; 2017 May; 7(1):2509. PubMed ID: 28559539
[TBL] [Abstract][Full Text] [Related]
18. Computational refinement identifies functional destructive single nucleotide polymorphisms associated with human retinoid X receptor gene.
Sarkar S; Gupta VK; Sharma S; Shen T; Gupta V; Mirzaei M; Graham SL; Chitranshi N
J Biomol Struct Dyn; 2023 Mar; 41(4):1458-1478. PubMed ID: 34971346
[TBL] [Abstract][Full Text] [Related]
19. In-Silico analysis of missense SNPs in Human HPPD gene associated with Tyrosinemia type III and Hawkinsinuria.
Naveed M; Tehreem S; Mehboob MZ
Comput Biol Chem; 2019 Jun; 80():284-291. PubMed ID: 31054541
[TBL] [Abstract][Full Text] [Related]
20. Identification of the SIRT1 gene's most harmful non-synonymous SNPs and their effects on functional and structural features-an
Thayyil Menambath D; Adiga U; Rai T; Adiga S; Shetty V
F1000Res; 2023; 12():66. PubMed ID: 38283900
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
