BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

302 related articles for article (PubMed ID: 8582049)

  • 41. [Past, present, and future in Leber's hereditary optic neuropathy].
    Oguchi Y
    Nippon Ganka Gakkai Zasshi; 2001 Dec; 105(12):809-27. PubMed ID: 11802455
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population.
    Dogulu CF; Kansu T; Seyrantepe V; Ozguc M; Topaloglu H; Johns DR
    Eye (Lond); 2001 Apr; 15(Pt 2):183-8. PubMed ID: 11339587
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The usefulness of single-strand DNA conformation polymorphism analysis to detect mutations in protein C deficiency.
    Gómez E; Poort SR; Bertina RM; Reitsma PH
    Blood Coagul Fibrinolysis; 1997 Nov; 8(8):497-502. PubMed ID: 9491267
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Identification of novel mutations in five patients with mitochondrial encephalomyopathy.
    Valente L; Piga D; Lamantea E; Carrara F; Uziel G; Cudia P; Zani A; Farina L; Morandi L; Mora M; Spinazzola A; Zeviani M; Tiranti V
    Biochim Biophys Acta; 2009 May; 1787(5):491-501. PubMed ID: 18977334
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism.
    Jorge SB; Melo MB; Costa FF; Sonati MF
    Braz J Med Biol Res; 2003 Nov; 36(11):1471-4. PubMed ID: 14576901
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mitochondrial DNA point mutations and a novel deletion induced by direct low-LET radiation and by medium from irradiated cells.
    Murphy JE; Nugent S; Seymour C; Mothersill C
    Mutat Res; 2005 Aug; 585(1-2):127-36. PubMed ID: 16002327
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS; Herbert J; Sadiq SA; Miller JR; Madonna M; Hirano M
    Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH; Tong Y; Li BH; Chen YK
    Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation.
    Isashiki Y; Sonoda S; Izumo S; Sakamoto T; Tachikui H; Inoue I
    Ophthalmic Res; 2003; 35(4):224-31. PubMed ID: 12815198
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M; Muntoni F; Savarese N; Serra G; Tiranti V; Carrara F; Mariotti C; DiDonato S
    Eur J Hum Genet; 1993; 1(1):80-7. PubMed ID: 8069654
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Accumulation of mitochondrial DNA mutations in human immunodeficiency virus-infected patients treated with nucleoside-analogue reverse-transcriptase inhibitors.
    Martin AM; Hammond E; Nolan D; Pace C; Den Boer M; Taylor L; Moore H; Martinez OP; Christiansen FT; Mallal S
    Am J Hum Genet; 2003 Mar; 72(3):549-60. PubMed ID: 12587093
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies].
    Xu JB; Ma YN; Pan H; Zheng XF; Zhang Y; Wang ST; Bu DF; Qi Y
    Zhonghua Yi Xue Za Zhi; 2011 Apr; 91(14):969-72. PubMed ID: 21609548
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Rapid and effective detection of mutations in the p53 gene using nonradioactive single-strand conformation polymorphism (SSCP) technique applied on PhastSystem.
    Kurvinen K; Hietanen S; Syrjänen K; Syrjänen S
    J Virol Methods; 1995 Jan; 51(1):43-53. PubMed ID: 7730436
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresis.
    Chen TJ; Boles RG; Wong LJ
    Clin Chem; 1999 Aug; 45(8 Pt 1):1162-7. PubMed ID: 10430780
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathy.
    Verma A; Piccoli DA; Bonilla E; Berry GT; DiMauro S; Moraes CT
    Pediatr Res; 1997 Oct; 42(4):448-54. PubMed ID: 9380435
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Recent developments in the molecular genetics of mitochondrial disorders.
    Graeber MB; Müller U
    J Neurol Sci; 1998 Jan; 153(2):251-63. PubMed ID: 9511882
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
    Shoffner JM; Bialer MG; Pavlakis SG; Lott M; Kaufman A; Dixon J; Teichberg S; Wallace DC
    Neurology; 1995 Feb; 45(2):286-92. PubMed ID: 7854527
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Extensive mtDNA diversity in horses revealed by PCR-SSCP analysis.
    Marklund S; Chaudhary R; Marklund L; Sandberg K; Andersson L
    Anim Genet; 1995 Jun; 26(3):193-6. PubMed ID: 7793689
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Design and use of a peptide nucleic acid for detection of the heteroplasmic low-frequency mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) mutation in human mitochondrial DNA.
    Hancock DK; Schwarz FP; Song F; Wong LJ; Levin BC
    Clin Chem; 2002 Dec; 48(12):2155-63. PubMed ID: 12446471
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel approach for rapid screening of mitochondrial D310 polymorphism.
    Aral C; Kaya H; Ataizi-Celikel C; Akkiprik M; Sonmez O; Gulluoglu BM; Ozer A
    BMC Cancer; 2006 Jan; 6():21. PubMed ID: 16433919
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.