381 related articles for article (PubMed ID: 30676783)
21. In-Silico Analyses of Nonsynonymous Variants in the BRCA1 Gene.
Arshad S; Ishaque I; Mumtaz S; Rashid MU; Malkani N
Biochem Genet; 2021 Dec; 59(6):1506-1526. PubMed ID: 33945048
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Plasma homocysteine concentrations and the single nucleotide polymorphisms in the methionine synthase gene (MTR 2756A>G): Associations with the polycystic ovary syndrome An observational study.
Palep-Singh M; Picton HM; Yates ZR; Barth JH; Balen AH
Eur J Obstet Gynecol Reprod Biol; 2008 Jun; 138(2):180-6. PubMed ID: 18281142
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Identification of deleterious nsSNPs in human HGF gene: in silico approach.
Hoda A; Lika Çekani M; Kolaneci V
J Biomol Struct Dyn; 2023; 41(21):11889-11903. PubMed ID: 36598356
[TBL] [Abstract][Full Text] [Related]
26. Levels of key enzymes of methionine-homocysteine metabolism in preeclampsia.
Pérez-Sepúlveda A; España-Perrot PP; Fernández XB; Ahumada V; Bustos V; Arraztoa JA; Dobierzewska A; Figueroa-Diesel H; Rice GE; Illanes SE
Biomed Res Int; 2013; 2013():731962. PubMed ID: 24024209
[TBL] [Abstract][Full Text] [Related]
27. In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract.
Wang Z; Huang C; Lv H; Zhang M; Li X
PLoS One; 2020; 15(1):e0227859. PubMed ID: 31935276
[TBL] [Abstract][Full Text] [Related]
28.
Pavithran H; Kumavath R
J Genet; 2021; 100():. PubMed ID: 34187970
[TBL] [Abstract][Full Text] [Related]
29. Identification of most damaging nsSNPs in human CCR6 gene: In silico analyses.
Akhtar M; Jamal T; Jamal H; Din JU; Jamal M; Arif M; Arshad M; Jalil F
Int J Immunogenet; 2019 Dec; 46(6):459-471. PubMed ID: 31364806
[TBL] [Abstract][Full Text] [Related]
30. Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia.
Fofou-Caillierez MB; Mrabet NT; Chéry C; Dreumont N; Flayac J; Pupavac M; Paoli J; Alberto JM; Coelho D; Camadro JM; Feillet F; Watkins D; Fowler B; Rosenblatt DS; Guéant JL
Hum Mol Genet; 2013 Nov; 22(22):4591-601. PubMed ID: 23825108
[TBL] [Abstract][Full Text] [Related]
31. In Silico Analysis of Coding/Noncoding SNPs of Human
Elkhattabi L; Morjane I; Charoute H; Amghar S; Bouafi H; Elkarhat Z; Saile R; Rouba H; Barakat A
J Diabetes Res; 2019; 2019():4951627. PubMed ID: 31236417
[TBL] [Abstract][Full Text] [Related]
32. Prediction of deleterious functional effects of non-synonymous single nucleotide polymorphisms in human nuclear receptor genes using a bioinformatics approach.
Liu YH; Li CG; Zhou SF
Drug Metab Lett; 2009 Dec; 3(4):242-86. PubMed ID: 20050372
[TBL] [Abstract][Full Text] [Related]
33. In silico analysis of nonsynonymous single nucleotide polymorphisms of the human adiponectin receptor 2 (ADIPOR2) gene.
Solayman M; Saleh MA; Paul S; Khalil MI; Gan SH
Comput Biol Chem; 2017 Jun; 68():175-185. PubMed ID: 28359874
[TBL] [Abstract][Full Text] [Related]
34. Methylenetetrahydrofolate reductase C677T and methionine synthase A2756G polymorphisms influence on leukocyte genomic DNA methylation level.
Weiner AS; Boyarskikh UA; Voronina EN; Mishukova OV; Filipenko ML
Gene; 2014 Jan; 533(1):168-72. PubMed ID: 24103477
[TBL] [Abstract][Full Text] [Related]
35. Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach.
Bouatrous E; Nouira S; Menif S; Ouragini H
Mol Syndromol; 2023 Oct; 14(5):375-393. PubMed ID: 37901856
[TBL] [Abstract][Full Text] [Related]
36. The effects of non-synonymous single nucleotide polymorphisms (nsSNPs) on protein-protein interactions.
Yates CM; Sternberg MJ
J Mol Biol; 2013 Nov; 425(21):3949-63. PubMed ID: 23867278
[TBL] [Abstract][Full Text] [Related]
37. Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins.
Savas S; Ahmad MF; Shariff M; Kim DY; Ozcelik H
Proteins; 2005 Feb; 58(3):697-705. PubMed ID: 15617026
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
Wang LL; Li Y; Zhou SF
Drug Metab Dispos; 2009 May; 37(5):977-91. PubMed ID: 19204079
[TBL] [Abstract][Full Text] [Related]
40. Computational Analysis of Missense Variants in the Human Transmembrane Protease Serine 2 (
Saih A; Bouqdayr M; Baba H; Hamdi S; Moussamih S; Bennani H; Saile R; Wakrim L; Kettani A
Biomed Res Int; 2021; 2021():9982729. PubMed ID: 34692848
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
