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Journal Abstract Search

213 related items for PubMed ID: 22199290

  • 41. Detection of mitochondrial DNA mutations by high-throughput sequencing in the blood of breast cancer patients.
    Li LH, Kang T, Chen L, Zhang W, Liao Y, Chen J, Shi Y.
    Int J Mol Med; 2014 Jan; 33(1):77-82. PubMed ID: 24253185
    [Abstract] [Full Text] [Related]

  • 42. Mutations in the D-loop region and increased copy number of mitochondrial DNA in human laryngeal squamous cell carcinoma.
    Guo W, Yang D, Xu H, Zhang Y, Huang J, Yang Z, Chen X, Huang Z.
    Mol Biol Rep; 2013 Jan; 40(1):13-20. PubMed ID: 23114912
    [Abstract] [Full Text] [Related]

  • 43. Identification of somatic and germline mitochondrial DNA sequence variants in prostate cancer patients.
    Gómez-Zaera M, Abril J, González L, Aguiló F, Condom E, Nadal M, Nunes V.
    Mutat Res; 2006 Mar 20; 595(1-2):42-51. PubMed ID: 16472830
    [Abstract] [Full Text] [Related]

  • 44. Frequent mutations in the mitochondrial control region DNA in breast tissue.
    Rosson D, Keshgegian AA.
    Cancer Lett; 2004 Nov 08; 215(1):89-94. PubMed ID: 15374637
    [Abstract] [Full Text] [Related]

  • 45. Rapid identification of mtDNA somatic mutations in gastric cancer tissues based on the mtDNA phylogeny.
    Bi R, Li WL, Chen MQ, Zhu Z, Yao YG.
    Mutat Res; 2011 May 10; 709-710():15-20. PubMed ID: 21419139
    [Abstract] [Full Text] [Related]

  • 46. Analysis of potential cancer biomarkers in mitochondrial DNA.
    Jakupciak JP, Dakubo GD, Maragh S, Parr RL.
    Curr Opin Mol Ther; 2006 Dec 10; 8(6):500-6. PubMed ID: 17243485
    [Abstract] [Full Text] [Related]

  • 47. Detection of mitochondrial DNA mutations in gestational trophoblastic disease.
    Chiu PM, Liu VW, Ngan HY, Khoo US, Cheung AN.
    Hum Mutat; 2003 Aug 10; 22(2):177. PubMed ID: 12872261
    [Abstract] [Full Text] [Related]

  • 48. Analysis of fluorescence in situ hybridization, mtDNA quantification, and mtDNA sequence for the detection of early bladder cancer.
    Yoo JH, Suh B, Park TS, Shin MG, Choi YD, Lee CH, Choi JR.
    Cancer Genet Cytogenet; 2010 Apr 15; 198(2):107-17. PubMed ID: 20362225
    [Abstract] [Full Text] [Related]

  • 49. Mitochondrial DNA mutations in patients with HRHPV-related cervical lesions.
    Goia-Ruşanu CD, Iancu IV, Botezatu A, Socolov D, Huică I, Pleşa A, Anton G.
    Roum Arch Microbiol Immunol; 2011 Apr 15; 70(1):5-10. PubMed ID: 21717805
    [Abstract] [Full Text] [Related]

  • 50. Mitochondrial NADH-dehydrogenase polymorphisms as sporadic breast cancer risk factor.
    Czarnecka AM, Klemba A, Krawczyk T, Zdrozny M, Arnold RS, Bartnik E, Petros JA.
    Oncol Rep; 2010 Feb 15; 23(2):531-5. PubMed ID: 20043118
    [Abstract] [Full Text] [Related]

  • 51. Use of sequence variation in three highly variable regions of the mitochondrial DNA for the discrimination of allogeneic platelets.
    Warner JB, Bruin EJ, Hannig H, Hellenkamp F, Hörning A, Mittmann K, van der Steege G, de Leij LF, Garritsen HS.
    Transfusion; 2006 Apr 15; 46(4):554-61. PubMed ID: 16584431
    [Abstract] [Full Text] [Related]

  • 52. Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.
    Darvishi K, Sharma S, Bhat AK, Rai E, Bamezai RN.
    Cancer Lett; 2007 May 08; 249(2):249-55. PubMed ID: 17081685
    [Abstract] [Full Text] [Related]

  • 53. Frequent somatic mutations of mitochondrial DNA in esophageal squamous cell carcinoma.
    Kumimoto H, Yamane Y, Nishimoto Y, Fukami H, Shinoda M, Hatooka S, Ishizaki K.
    Int J Cancer; 2004 Jan 10; 108(2):228-31. PubMed ID: 14639607
    [Abstract] [Full Text] [Related]

  • 54. Control region mutations and the 'common deletion' are frequent in the mitochondrial DNA of patients with esophageal squamous cell carcinoma.
    Abnet CC, Huppi K, Carrera A, Armistead D, McKenney K, Hu N, Tang ZZ, Taylor PR, Dawsey SM.
    BMC Cancer; 2004 Jul 01; 4():30. PubMed ID: 15230979
    [Abstract] [Full Text] [Related]

  • 55. Somatic mutation in mitochondrial DNA and nuclear microsatellite instability in gastric cancer.
    Hiyama T, Tanaka S, Shima H, Kose K, Tuncel H, Ito M, Kitadai Y, Sumii M, Yoshihara M, Shimamoto F, Haruma K, Chayama K.
    Oncol Rep; 2003 Jul 01; 10(6):1837-41. PubMed ID: 14534705
    [Abstract] [Full Text] [Related]

  • 56. Detection of mitochondrial DNA mutations in the tumor and cerebrospinal fluid of medulloblastoma patients.
    Wong LJ, Lueth M, Li XN, Lau CC, Vogel H.
    Cancer Res; 2003 Jul 15; 63(14):3866-71. PubMed ID: 12873974
    [Abstract] [Full Text] [Related]

  • 57. Nuclear and mitochondrial genome instability in human breast cancer.
    Richard SM, Bailliet G, Páez GL, Bianchi MS, Peltomäki P, Bianchi NO.
    Cancer Res; 2000 Aug 01; 60(15):4231-7. PubMed ID: 10945635
    [Abstract] [Full Text] [Related]

  • 58. Decreased copy number of mitochondrial DNA in Ewing's sarcoma.
    Yu M, Wan Y, Zou Q.
    Clin Chim Acta; 2010 May 02; 411(9-10):679-83. PubMed ID: 20123091
    [Abstract] [Full Text] [Related]

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  • 60. Tandem duplication/triplication correlated with poly-cytosine stretch variation in human mitochondrial DNA D-loop region.
    Hung WY, Lin JC, Lee LM, Wu CW, Tseng LM, Yin PH, Chi CW, Lee HC.
    Mutagenesis; 2008 Mar 02; 23(2):137-42. PubMed ID: 18252697
    [Abstract] [Full Text] [Related]

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