BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

323 related articles for article (PubMed ID: 34234628)

  • 21. 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]  

  • 22. Prediction of potential deleterious nonsynonymous single nucleotide polymorphisms of HIF1A gene: A computational approach.
    Jamali Z; Taheri-Anganeh M; Entezam M
    Comput Biol Chem; 2020 Oct; 88():107354. PubMed ID: 32801061
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Genetics and lymphoedema: a future yet to be fully discovered.
    Cooper G
    Br J Community Nurs; 2017 Jan; 22(1):646-648. PubMed ID: 28034335
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. Computational analysis for the determination of deleterious nsSNPs in human MTHFD1 gene.
    Desai M; Chauhan JB
    Comput Biol Chem; 2017 Oct; 70():7-14. PubMed ID: 28734179
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes.
    Ivanovski I; Akbaroghli S; Pollazzon M; Gelmini C; Caraffi SG; Mansouri M; Chavoshzadeh Z; Rosato S; Polizzi V; Gargano G; Alders M; Garavelli L; Hennekam RC
    Am J Med Genet A; 2018 May; 176(5):1166-1174. PubMed ID: 29681106
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B; Hersh JH
    Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.
    Alders M; Mendola A; Adès L; Al Gazali L; Bellini C; Dallapiccola B; Edery P; Frank U; Hornshuh F; Huisman SA; Jagadeesh S; Kayserili H; Keng WT; Lev D; Prada CE; Sampson JR; Schmidtke J; Shashi V; van Bever Y; Van der Aa N; Verhagen JM; Verheij JB; Vikkula M; Hennekam RC
    Mol Syndromol; 2013 Mar; 4(3):107-13. PubMed ID: 23653581
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. [Hennekam syndrome: a case report and review of literature].
    Zhang N; Shen WB; Cai HC; Yan XM; Liu SL; Wu D; Sun G; Qian JM; Dun ZN; Zhao YQ
    Zhonghua Nei Ke Za Zhi; 2013 Mar; 52(3):192-6. PubMed ID: 23856108
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. CCBE1 is essential for mammalian lymphatic vascular development and enhances the lymphangiogenic effect of vascular endothelial growth factor-C in vivo.
    Bos FL; Caunt M; Peterson-Maduro J; Planas-Paz L; Kowalski J; Karpanen T; van Impel A; Tong R; Ernst JA; Korving J; van Es JH; Lammert E; Duckers HJ; Schulte-Merker S
    Circ Res; 2011 Aug; 109(5):486-91. PubMed ID: 21778431
    [TBL] [Abstract][Full Text] [Related]  

  • 40. CCBE1 enhances lymphangiogenesis via A disintegrin and metalloprotease with thrombospondin motifs-3-mediated vascular endothelial growth factor-C activation.
    Jeltsch M; Jha SK; Tvorogov D; Anisimov A; Leppänen VM; Holopainen T; Kivelä R; Ortega S; Kärpanen T; Alitalo K
    Circulation; 2014 May; 129(19):1962-71. PubMed ID: 24552833
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.