106 related articles for article (PubMed ID: 38858637)
1. 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]
2. 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]
3. In-Silico Computing of the Most Deleterious nsSNPs in HBA1 Gene.
AbdulAzeez S; Borgio JF
PLoS One; 2016; 11(1):e0147702. PubMed ID: 26824843
[TBL] [Abstract][Full Text] [Related]
4. Screening and insilico analysis of deleterious nsSNPs (missense) in human CSF3 for their effects on protein structure, stability and function.
Guttula PK; Chandrasekaran G; Gupta MK
Comput Biol Chem; 2019 Oct; 82():57-64. PubMed ID: 31272062
[TBL] [Abstract][Full Text] [Related]
5. A computational in silico approach to predict high-risk coding and non-coding SNPs of human PLCG1 gene.
Khan SM; Faisal AM; Nila TA; Binti NN; Hosen MI; Shekhar HU
PLoS One; 2021; 16(11):e0260054. PubMed ID: 34793541
[TBL] [Abstract][Full Text] [Related]
6. Predicting the functional and structural consequences of nsSNPs in human methionine synthase gene using computational tools.
Desai M; Chauhan JB
Syst Biol Reprod Med; 2019 Aug; 65(4):288-300. PubMed ID: 30676783
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Structural Consequences of IRS-2 nsSNPs and Implication for Insulin Receptor Substrate-2 Protein Stability.
Zia A; Shams S; Shah M; Afridi SG; Khan A
Biochem Genet; 2023 Feb; 61(1):69-86. PubMed ID: 35727487
[TBL] [Abstract][Full Text] [Related]
9. Prediction of deleterious non-synonymous SNPs of human MDC1 gene: an in silico approach.
Thote V; Dinesh S; Sharma S
Syst Biol Reprod Med; 2024 Dec; 70(1):101-112. PubMed ID: 38630598
[TBL] [Abstract][Full Text] [Related]
10. In silico prediction of deleterious non-synonymous SNPs in
Ajith A; Subbiah U
Asian Biomed (Res Rev News); 2023 Aug; 17(4):185-199. PubMed ID: 37860678
[TBL] [Abstract][Full Text] [Related]
11. Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach.
George Priya Doss C; Nagasundaram N; Chakraborty C; Chen L; Zhu H
Hum Genomics; 2013 Apr; 7(1):10. PubMed ID: 23561625
[TBL] [Abstract][Full Text] [Related]
12. Determination of deleterious single-nucleotide polymorphisms of human LYZ C gene: an in silico study.
Venkata Subbiah H; Ramesh Babu P; Subbiah U
J Genet Eng Biotechnol; 2022 Jul; 20(1):92. PubMed ID: 35776277
[TBL] [Abstract][Full Text] [Related]
13. Assessment of structurally and functionally high-risk nsSNPs impacts on human bone morphogenetic protein receptor type IA (BMPR1A) by computational approach.
Islam MJ; Parves MR; Mahmud S; Tithi FA; Reza MA
Comput Biol Chem; 2019 Jun; 80():31-45. PubMed ID: 30884445
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A comprehensive in Silico analysis of the functional and structural impact of single nucleotide polymorphisms (SNPs) in the human IL-33 gene.
Falahi S; Karaji AG; Koohyanizadeh F; Rezaiemanesh A; Salari F
Comput Biol Chem; 2021 Oct; 94():107560. PubMed ID: 34455166
[TBL] [Abstract][Full Text] [Related]
16. Prediction and Structural Comparison of Deleterious Coding Nonsynonymous Single Nucleotide Polymorphisms (nsSNPs) in Human LEP Gene Associated with Obesity.
Bouafi H; Bencheikh S; Mehdi Krami AL; Morjane I; Charoute H; Rouba H; Saile R; Benhnini F; Barakat A
Biomed Res Int; 2019; 2019():1832084. PubMed ID: 31871931
[TBL] [Abstract][Full Text] [Related]
17. Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis.
Shinwari K; Guojun L; Deryabina SS; Bolkov MA; Tuzankina IA; Chereshnev VA
ScientificWorldJournal; 2021; 2021():6642626. PubMed ID: 34234628
[TBL] [Abstract][Full Text] [Related]
18. Structure analysis of deleterious nsSNPs in human PALB2 protein for functional inference.
Nawar N; Paul A; Mahmood HN; Faisal MI; Hosen MI; Shekhar HU
Bioinformation; 2021; 17(3):424-438. PubMed ID: 34092963
[TBL] [Abstract][Full Text] [Related]
19. Simulation Based Investigation of Deleterious nsSNPs in ATXN2 Gene and Its Structural Consequence Toward Spinocerebellar Ataxia.
Sinha S; Verma S; Singh A; Somvanshi P; Grover A
J Cell Biochem; 2018 Jan; 119(1):499-510. PubMed ID: 28612427
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]