These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 15251970

  • 1. A new technology for mutation detection.
    Shackelford W, Deng S, Murayama K, Wang J.
    Ann N Y Acad Sci; 2004 Jun; 1022():257-62. PubMed ID: 15251970
    [Abstract] [Full Text] [Related]

  • 2. RNA mutations of prox1 detected in human esophageal cancer cells by the shifted termination assay.
    Yoshimoto T, Takahashi M, Nagayama S, Watanabe G, Shimada Y, Sakasi Y, Kubo H.
    Biochem Biophys Res Commun; 2007 Jul 27; 359(2):258-62. PubMed ID: 17533110
    [Abstract] [Full Text] [Related]

  • 3. Wild-type blocking polymerase chain reaction for detection of single nucleotide minority mutations from clinical specimens.
    Dominguez PL, Kolodney MS.
    Oncogene; 2005 Oct 13; 24(45):6830-4. PubMed ID: 16116485
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 13; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Detection of hotspot mutations and polymorphisms using an enhanced PCR-RFLP approach.
    Liu WH, Kaur M, Makrigiorgos GM.
    Hum Mutat; 2003 May 13; 21(5):535-41. PubMed ID: 12673796
    [Abstract] [Full Text] [Related]

  • 9. From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms.
    Syvänen AC.
    Hum Mutat; 1999 May 13; 13(1):1-10. PubMed ID: 9888384
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. A highly sensitive detection method for somatic mutations in p53 gene.
    Sato T, Sato A, Ishihara H, Konishi K.
    Rinsho Byori; 2003 Feb 13; 51(2):98-106. PubMed ID: 12690626
    [Abstract] [Full Text] [Related]

  • 14. Serial processing of biological reactions using flow-through microfluidic devices: coupled PCR/LDR for the detection of low-abundant DNA point mutations.
    Hashimoto M, Barany F, Xu F, Soper SA.
    Analyst; 2007 Sep 13; 132(9):913-21. PubMed ID: 17710267
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Application of oligonucleotide microarray primer extension to detection of p53 single nucleotide polymorphisms].
    Wu QH, Ma WL, Zhang B, Guo QY, Li L, Zheng WL.
    Ai Zheng; 2005 Jul 15; 24(7):898-902. PubMed ID: 16004824
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Simple polymerase chain reaction for the detection of mutations and deletions in the epidermal growth factor receptor gene: applications of this method for the diagnosis of non-small-cell lung cancer.
    Uhara M, Matsuda K, Taira C, Higuchi Y, Okumura N, Yamauchi K.
    Clin Chim Acta; 2009 Mar 15; 401(1-2):68-72. PubMed ID: 19063875
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.