BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 37322437)

  • 1. In-silico assessment of high-risk non-synonymous SNPs in ADAMTS3 gene associated with Hennekam syndrome and their impact on protein stability and function.
    Shinwari K; Wu Y; Rehman HM; Xiao N; Bolkov M; Tuzankina I; Chereshnev V
    BMC Bioinformatics; 2023 Jun; 24(1):251. PubMed ID: 37322437
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. An additional case of Hennekam lymphangiectasia-lymphedema syndrome caused by loss-of-function mutation in ADAMTS3.
    Scheuerle AE; Sweed NT; Timmons CF; Smith ED; Alcaraz WA; Shinde DN
    Am J Med Genet A; 2018 Dec; 176(12):2858-2861. PubMed ID: 30450763
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3.
    Brouillard P; Dupont L; Helaers R; Coulie R; Tiller GE; Peeden J; Colige A; Vikkula M
    Hum Mol Genet; 2017 Nov; 26(21):4095-4104. PubMed ID: 28985353
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Comprehensive
    Hoda A; Berisha B; Bixheku X; Zanchi FB
    J Biomol Struct Dyn; 2024 Apr; ():1-17. PubMed ID: 38656135
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular Modelling and Dynamics Study of nsSNP in STXBP1 Gene in Early Infantile Epileptic Encephalopathy Disease.
    Al Mehdi K; Fouad B; Zouhair E; Boutaina B; Yassine N; Chaimaa AEC; Najat S; Hassan R; Rachida R; Abdelhamid B; Halima N
    Biomed Res Int; 2019; 2019():4872101. PubMed ID: 31976320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome.
    Boone PM; Paterson S; Mohajeri K; Zhu W; Genetti CA; Tai DJC; Nori N; Agrawal PB; Bacino CA; Bi W; Talkowski ME; Hogan BM; Rodan LH
    Am J Med Genet A; 2020 Jan; 182(1):189-194. PubMed ID: 31633297
    [TBL] [Abstract][Full Text] [Related]  

  • 10. In silico analyses of Wnt1 nsSNPs reveal structurally destabilizing variants, altered interactions with Frizzled receptors and its deregulation in tumorigenesis.
    Mondal A; Paul D; Dastidar SG; Saha T; Goswami AM
    Sci Rep; 2022 Sep; 12(1):14934. PubMed ID: 36056132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Identification of the most damaging nsSNPs in the human CFL1 gene and their functional and structural impacts on cofilin-1 protein.
    Halder SK; Rafi MO; Shahriar EB; Albogami S; El-Shehawi AM; Daullah SMMU; Himel MK; Emran TB
    Gene; 2022 Apr; 819():146206. PubMed ID: 35092861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. In silico analysis of non-synonymous single nucleotide polymorphisms (nsSNPs) in the human GJA3 gene associated with congenital cataract.
    Zhang M; Huang C; Wang Z; Lv H; Li X
    BMC Mol Cell Biol; 2020 Mar; 21(1):12. PubMed ID: 32143568
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Comprehensive Characterization of the Coding and Non-Coding Single Nucleotide Polymorphisms in the Tumor Protein p63 (TP63) Gene Using In Silico Tools.
    Akter S; Hossain S; Ali MA; Hosen MI; Shekhar HU
    Biomolecules; 2021 Nov; 11(11):. PubMed ID: 34827731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX gene.
    Arifuzzaman M; Mitra S; Das R; Hamza A; Absar N; Dash R
    Ann Hum Genet; 2020 Jan; 84(1):54-71. PubMed ID: 31583691
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Computational identification of pathogenic associated nsSNPs and its structural impact in UROD gene: a molecular dynamics approach.
    Doss CG; Magesh R
    Cell Biochem Biophys; 2014 Nov; 70(2):735-46. PubMed ID: 24777812
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.