BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 8755922)

  • 1. Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.
    Andreassen R; Egeland T; Olaisen B
    Am J Hum Genet; 1996 Aug; 59(2):360-7. PubMed ID: 8755922
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo mutations and allelic diversity at minisatellite locus D7S22 investigated by allele-specific four-state MVR-PCR analysis.
    Andreassen R; Olaisen B
    Hum Mol Genet; 1998 Dec; 7(13):2113-20. PubMed ID: 9817929
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Length and sequence variation in D7S22 (g3) alleles studied by high resolution length measurements and nucleotide sequencing.
    Andreassen R; Olaisen B
    Electrophoresis; 1997 May; 18(5):675-81. PubMed ID: 9194589
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation at minisatellite locus DYF155S1: allele length mutation rate is affected by age of progenitor.
    Andreassen R; Lundsted J; Olaisen B
    Electrophoresis; 2002 Aug; 23(15):2377-83. PubMed ID: 12210191
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309).
    May CA; Jeffreys AJ; Armour JA
    Hum Mol Genet; 1996 Nov; 5(11):1823-33. PubMed ID: 8923012
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nucleotide sequence analysis of the apolipoprotein B 3' VNTR.
    Ellsworth DL; Shriver MD; Boerwinkle E
    Hum Mol Genet; 1995 May; 4(5):937-44. PubMed ID: 7633455
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism.
    Monckton DG; Neumann R; Guram T; Fretwell N; Tamaki K; MacLeod A; Jeffreys AJ
    Nat Genet; 1994 Oct; 8(2):162-70. PubMed ID: 7842015
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A HinfI polymorphism in the 5' flanking region of the human VNTR locus D1S80.
    Alonso A; Martin P; Albarrán C; Sancho M
    Int J Legal Med; 1995; 107(4):216-8. PubMed ID: 7599101
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping.
    Neil DL; Jeffreys AJ
    Hum Mol Genet; 1993 Aug; 2(8):1129-35. PubMed ID: 8401494
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characteristics of mutations at the D5S818 locus studied with a tightly linked marker.
    Edwards M; Allen RW
    Transfusion; 2004 Jan; 44(1):83-90. PubMed ID: 14692972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distinguishing minisatellite mutation from non-paternity by MVR-PCR.
    Tamaki K; Brenner CH; Jeffreys AJ
    Forensic Sci Int; 2000 Sep; 113(1-3):55-62. PubMed ID: 10978602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Insulin gene 5' flanking polymorphism. Length of class 1 alleles in number of repeat units.
    McGinnis RE; Spielman RS
    Diabetes; 1995 Nov; 44(11):1296-302. PubMed ID: 7589827
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of allelic drop-out at short tandem repeat loci].
    Chen WJ; Li Y; Wu XJ; Zhang YM; Liu SJ; Chen Y; Chen WH; Sun HY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun; 29(3):360-3. PubMed ID: 22678808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability.
    Armour JA; Harris PC; Jeffreys AJ
    Hum Mol Genet; 1993 Aug; 2(8):1137-45. PubMed ID: 8401495
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA-minisatellite mutations: recent investigations concerning distribution and impact on parentage testing.
    Henke J; Fimmers R; Baur MP; Henke L
    Int J Legal Med; 1993; 105(4):217-22. PubMed ID: 8094296
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Allelic structures at hypervariable minisatellite B6.7 in Japanese show population specificity.
    Mizukoshi T; Tamaki K; Azumi J; Matsumoto H; Imai K; Jeffreys AJ
    J Hum Genet; 2002; 47(5):232-8. PubMed ID: 12032590
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Allele-specific MVR-PCR analysis at minisatellite D1S8.
    Monckton DG; Tamaki K; MacLeod A; Neil DL; Jeffreys AJ
    Hum Mol Genet; 1993 May; 2(5):513-9. PubMed ID: 8518788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7.
    Tamaki K; May CA; Dubrova YE; Jeffreys AJ
    Hum Mol Genet; 1999 May; 8(5):879-88. PubMed ID: 10196378
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Minisatellite and microsatellite length variation at a complex bovine VNTR locus.
    Nave A; Kashi Y; Soller M
    Anim Genet; 1997 Feb; 28(1):52-4. PubMed ID: 9124709
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene.
    Naito E; Dewa K; Fukuda M; Sumi H; Wakabayashi Y; Umetsu K; Yuasa I; Yamanouchi H
    J Forensic Sci; 2003 Nov; 48(6):1275-9. PubMed ID: 14640270
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.