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Journal Abstract Search

187 related items for PubMed ID: 17406573

  • 1. Mutation screening using fluorescence multiplex denaturing gradient gel electrophoresis (FMD): detecting mutations in the BRCA1 gene.
    Zhang S, Kuperstein G, Narod SA.
    Nat Protoc; 2006; 1(6):3101-10. PubMed ID: 17406573
    [Abstract] [Full Text] [Related]

  • 2. A fluorescent multiplex-DGGE screening test for mutations in the BRCA1 gene.
    Kuperstein G, Jack E, Narod SA.
    Genet Test; 2006; 10(1):1-7. PubMed ID: 16544996
    [Abstract] [Full Text] [Related]

  • 3. Two-dimensional gene scanning: exploring human genetic variability.
    Vijg J, van Orsouw NJ.
    Electrophoresis; 1999 Jun; 20(6):1239-49. PubMed ID: 10380764
    [Abstract] [Full Text] [Related]

  • 4. BRCA1 mutation screening using restriction endonuclease fingerprinting-single-strand conformation polymorphism in an automated capillary electrophoresis system.
    Kringen P, Egedal S, Pedersen JC, Harbitz TB, Tveit KM, Berg K, Børresen-Dale AL, Andersen TI.
    Electrophoresis; 2002 Dec; 23(24):4085-91. PubMed ID: 12481264
    [Abstract] [Full Text] [Related]

  • 5. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB).
    Azian M, Hapizah MN, Khalid BA, Khalid Y, Rosli A, Jamal R.
    Malays J Pathol; 2006 Jun; 28(1):7-15. PubMed ID: 17694954
    [Abstract] [Full Text] [Related]

  • 6. Mutational scanning of mitochondrial DNA by two-dimensional electrophoresis.
    van Orsouw NJ, Zhang X, Wei JY, Johns DR, Vijg J.
    Genomics; 1998 Aug 15; 52(1):27-36. PubMed ID: 9740668
    [Abstract] [Full Text] [Related]

  • 7. [CSNP discovery by two-dimensional gene scanning (TDGS)].
    Suh Y.
    Exp Mol Med; 2001 Apr 21; 33(1 Suppl):21-47. PubMed ID: 11708324
    [Abstract] [Full Text] [Related]

  • 8. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT.
    Hum Mutat; 2004 Jan 21; 23(1):57-66. PubMed ID: 14695533
    [Abstract] [Full Text] [Related]

  • 9. Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled amplicons.
    Ricevuto E, Sobol H, Stoppa-Lyonnet D, Gulino A, Marchetti P, Ficorella C, Martinotti S, Meo T, Tosi M.
    Clin Cancer Res; 2001 Jun 21; 7(6):1638-46. PubMed ID: 11410501
    [Abstract] [Full Text] [Related]

  • 10. Genetic diagnosis of 21-hydroxylase deficiency: DGGE-based mutation scanning of CYP21.
    Ohlsson G, Müller J, Schwartz M.
    Hum Mutat; 1999 Jun 21; 13(5):385-9. PubMed ID: 10338093
    [Abstract] [Full Text] [Related]

  • 11. Comprehensive mutation analysis of TSC1 using two-dimensional DNA electrophoresis with DGGE.
    Dabora SL, Sigalas I, Hall F, Eng C, Vijg J, Kwiatkowski DJ.
    Ann Hum Genet; 1998 Nov 21; 62(Pt 6):491-504. PubMed ID: 10363127
    [Abstract] [Full Text] [Related]

  • 12. [Methodological evaluation on PCR-DGGE technique in detecting DNA mutation and single nucleotide polymorphism].
    Lu XJ, Jia YQ, Fan H, Zhang L, Jia J.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2007 Sep 21; 38(5):882-4. PubMed ID: 17953384
    [Abstract] [Full Text] [Related]

  • 13. Denaturing gradient-based two-dimensional gene mutation scanning in a polymer microfluidic network.
    Buch JS, Rosenberger F, Highsmith WE, Kimball C, DeVoe DL, Lee CS.
    Lab Chip; 2005 Apr 21; 5(4):392-400. PubMed ID: 15791336
    [Abstract] [Full Text] [Related]

  • 14. Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene.
    Laprise SL, Mak EK, Killoran KA, Layman LC, Gray MR.
    Hum Mutat; 1998 Apr 21; 12(6):393-402. PubMed ID: 9829908
    [Abstract] [Full Text] [Related]

  • 15. Mutation detection by denaturing gradient gel electrophoresis (DGGE).
    Fodde R, Losekoot M.
    Hum Mutat; 1994 Apr 21; 3(2):83-94. PubMed ID: 8199599
    [Abstract] [Full Text] [Related]

  • 16. Analysis of TP53 gene mutations in human lung cancer: comparison of capillary electrophoresis single strand conformation polymorphism assay with denaturing gradient gel electrophoresis and direct sequencing.
    Holmila R, Husgafvel-Pursiainen K.
    Cancer Detect Prev; 2006 Apr 21; 30(1):1-6. PubMed ID: 16458448
    [Abstract] [Full Text] [Related]

  • 17. Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis.
    Lodewyckx L, Vandevyver C, Vandervorst C, Van Steenbergen W, Raus J, Michiels L.
    Hum Mutat; 2001 Sep 21; 18(3):243-50. PubMed ID: 11524735
    [Abstract] [Full Text] [Related]

  • 18. Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method.
    Casadei S, Cortesi L, Pensotti V, Radice P, Pierotti M, Amadori D, Calistri D.
    Br J Cancer; 2001 Sep 14; 85(6):845-9. PubMed ID: 11556835
    [Abstract] [Full Text] [Related]

  • 19. Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.
    Mumm S, Jones J, Finnegan P, Henthorn PS, Podgornik MN, Whyte MP.
    Mol Genet Metab; 2002 Feb 14; 75(2):143-53. PubMed ID: 11855933
    [Abstract] [Full Text] [Related]

  • 20. Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients.
    Duponchel C, Di Rocco C, Cicardi M, Tosi M.
    Hum Mutat; 2001 Feb 14; 17(1):61-70. PubMed ID: 11139243
    [Abstract] [Full Text] [Related]

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