BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 19429541)

  • 41. 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]  

  • 42. Exploration of deleterious single nucleotide polymorphisms in late-onset Alzheimer disease susceptibility genes.
    Masoodi TA; Al Shammari SA; Al-Muammar MN; Alhamdan AA; Talluri VR
    Gene; 2013 Jan; 512(2):429-37. PubMed ID: 22960267
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Predicting the impact of deleterious single point mutations in SMAD gene family using structural bioinformatics approach.
    George Priya Doss C; Nagasundaram N; Tanwar H
    Interdiscip Sci; 2012 Jun; 4(2):103-15. PubMed ID: 22843233
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Screening for deleterious nonsynonymous single-nucleotide polymorphisms in genes involved in steroid hormone metabolism and response.
    Johnson MM; Houck J; Chen C
    Cancer Epidemiol Biomarkers Prev; 2005 May; 14(5):1326-9. PubMed ID: 15894696
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Secondary and tertiary structure aberration of alpha globin chain in haemoglobin Q-India disorder.
    Wiwanitkit V
    Indian J Pathol Microbiol; 2006 Oct; 49(4):491-4. PubMed ID: 17183835
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The SAAPdb web resource: a large-scale structural analysis of mutant proteins.
    Hurst JM; McMillan LE; Porter CT; Allen J; Fakorede A; Martin AC
    Hum Mutat; 2009 Apr; 30(4):616-24. PubMed ID: 19191322
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders.
    Ponomarenko M; Sharypova E; Drachkova I; Chadaeva I; Arkova O; Podkolodnaya O; Ponomarenko P; Kolchanov N; Savinkova L
    BMC Med Genet; 2020 Oct; 21(Suppl 1):165. PubMed ID: 33092544
    [TBL] [Abstract][Full Text] [Related]  

  • 50. In silico prediction of deleterious single amino acid polymorphisms from amino acid sequence.
    Li S; Xi L; Li J; Wang C; Lei B; Shen Y; Liu H; Yao X; Li B
    J Comput Chem; 2011 May; 32(7):1211-6. PubMed ID: 21425278
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Statistical geometry approach to the study of functional effects of human nonsynonymous SNPs.
    Barenboim M; Jamison DC; Vaisman II
    Hum Mutat; 2005 Nov; 26(5):471-6. PubMed ID: 16200641
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A new insight into structural and functional impact of single-nucleotide polymorphisms in PTEN gene.
    George Priya Doss C; Rajith B
    Cell Biochem Biophys; 2013 Jun; 66(2):249-63. PubMed ID: 23161105
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Computer simulation of heterogeneous single nucleotide polymorphisms in the catalase gene indicates structural changes in the enzyme active site, NADPH-binding and tetramerization domains: a genetic predisposition for an altered catalase in patients with vitiligo?
    Wood JM; Gibbons NC; Chavan B; Schallreuter KU
    Exp Dermatol; 2008 Apr; 17(4):366-71. PubMed ID: 18315617
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Diagnostic approach to hemoglobinopathies.
    Kutlar F
    Hemoglobin; 2007; 31(2):243-50. PubMed ID: 17486507
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Three-dimensional structural location and molecular functional effects of missense SNPs in the T cell receptor Vbeta domain.
    Wang Z; Moult J
    Proteins; 2003 Nov; 53(3):748-57. PubMed ID: 14579365
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Use of in silico (computer) methods to predict and analyze the tertiary structure of plant hemoglobins.
    Gopalasubramaniam SK; Garrocho-Villegas V; Rivera GB; Pastor N; Arredondo-Peter R
    Methods Enzymol; 2008; 436():393-410. PubMed ID: 18237645
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Predicting deleterious non-synonymous single nucleotide polymorphisms in signal peptides based on hybrid sequence attributes.
    Qin W; Li Y; Li J; Yu L; Wu D; Jing R; Pu X; Guo Y; Li M
    Comput Biol Chem; 2012 Feb; 36():31-5. PubMed ID: 22277674
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Modelling and mutational evidence identify the substrate binding site and functional elements in APC amino acid transporters.
    Vangelatos I; Vlachakis D; Sophianopoulou V; Diallinas G
    Mol Membr Biol; 2009 Aug; 26(5):356-70. PubMed ID: 19670073
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiency.
    Saunders RE; Shiltagh N; Gomez K; Mellars G; Cooper C; Perry DJ; Tuddenham EG; Perkins SJ
    Thromb Haemost; 2009 Aug; 102(2):287-301. PubMed ID: 19652879
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.