183 related articles for article (PubMed ID: 28072499)
1. In silico analysis of the deleterious nsSNPs (missense) in the homeobox domain of human HOXB13 gene responsible for hereditary prostate cancer.
Chandrasekaran G; Hwang EC; Kang TW; Kwon DD; Park K; Lee JJ; Lakshmanan VK
Chem Biol Drug Des; 2017 Aug; 90(2):188-199. PubMed ID: 28072499
[TBL] [Abstract][Full Text] [Related]
2. Computational Modeling of complete HOXB13 protein for predicting the functional effect of SNPs and the associated role in hereditary prostate cancer.
Chandrasekaran G; Hwang EC; Kang TW; Kwon DD; Park K; Lee JJ; Lakshmanan VK
Sci Rep; 2017 Mar; 7():43830. PubMed ID: 28272408
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Computational analysis of non-synonymous single nucleotide polymorphism in the bovine
Hoda A; Bixheku X; Lika Çekani M
J Biomol Struct Dyn; 2024 May; 42(8):4155-4168. PubMed ID: 37278385
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. In silico approach to identify non-synonymous SNPs in human obesity related gene, MC3R (melanocortin-3-receptor).
Singh RK; Mahalingam K
Comput Biol Chem; 2017 Apr; 67():122-130. PubMed ID: 28073065
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Functional and structural analysis of non-synonymous single nucleotide polymorphisms (nsSNPs) in the MYB oncoproteins associated with human cancer.
Lim SW; Tan KJ; Azuraidi OM; Sathiya M; Lim EC; Lai KS; Yap WS; Afizan NARNM
Sci Rep; 2021 Dec; 11(1):24206. PubMed ID: 34921182
[TBL] [Abstract][Full Text] [Related]
9. In silico analysis of functional nsSNPs in human TRPC6 gene associated with steroid resistant nephrotic syndrome.
Joshi BB; Koringa PG; Mistry KN; Patel AK; Gang S; Joshi CG
Gene; 2015 Nov; 572(1):8-16. PubMed ID: 26127002
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Impacts of Nonsynonymous Single Nucleotide Polymorphisms of Adiponectin Receptor 1 Gene on Corresponding Protein Stability: A Computational Approach.
Saleh MA; Solayman M; Paul S; Saha M; Khalil MI; Gan SH
Biomed Res Int; 2016; 2016():9142190. PubMed ID: 27294143
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Structural investigation of deleterious non-synonymous SNPs of EGFR gene.
Raghav D; Sharma V; Agarwal SM
Interdiscip Sci; 2013 Mar; 5(1):60-8. PubMed ID: 23605641
[TBL] [Abstract][Full Text] [Related]
16. In silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.
Doss C GP
J Biomed Sci; 2012 Mar; 19(1):30. PubMed ID: 22423892
[TBL] [Abstract][Full Text] [Related]
17. Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.
Phani NM; Acharya S; Xavy S; Bhaskaranand N; Bhat MK; Jain A; Rai PS; Satyamoorthy K
Gene; 2014 Feb; 536(2):247-53. PubMed ID: 24378235
[TBL] [Abstract][Full Text] [Related]
18. The rs61742690 (S783N) single nucleotide polymorphism is a suitable target for disrupting BCL11A-mediated foetal-to-adult globin switching.
Abdulazeez S; Sultana S; Almandil NB; Almohazey D; Bency BJ; Borgio JF
PLoS One; 2019; 14(2):e0212492. PubMed ID: 30768627
[TBL] [Abstract][Full Text] [Related]
19. Computational analysis of high-risk SNPs in human CHK2 gene responsible for hereditary breast cancer: A functional and structural impact.
Badgujar NV; Tarapara BV; Shah FD
PLoS One; 2019; 14(8):e0220711. PubMed ID: 31398194
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
