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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 17614297)

  • 1. Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff.
    Schoenborn V; Gohlke H; Heid IM; Illig T; Utermann G; Kronenberg F
    Hum Mutat; 2007 Nov; 28(11):1141-9. PubMed ID: 17614297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MALDI-TOF MS and TaqMan assisted SNP genotyping of DNA isolated from formalin-fixed and paraffin-embedded tissues (FFPET).
    Jaremko M; Justenhoven C; Abraham BK; Schroth W; Fritz P; Brod S; Vollmert C; Illig T; Brauch H
    Hum Mutat; 2005 Mar; 25(3):232-8. PubMed ID: 15706592
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improved multiple displacement amplification with phi29 DNA polymerase for genotyping of single human cells.
    Kumar G; Garnova E; Reagin M; Vidali A
    Biotechniques; 2008 Jun; 44(7):879-90. PubMed ID: 18533898
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex whole genome amplified DNA generated from multiple DNA sources.
    Bergen AW; Haque KA; Qi Y; Beerman MB; Garcia-Closas M; Rothman N; Chanock SJ
    Hum Mutat; 2005 Sep; 26(3):262-70. PubMed ID: 16086324
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple displacement amplification to create a long-lasting source of DNA for genetic studies.
    Lovmar L; Syvänen AC
    Hum Mutat; 2006 Jul; 27(7):603-14. PubMed ID: 16786504
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tri-allelic SNP markers enable analysis of mixed and degraded DNA samples.
    Westen AA; Matai AS; Laros JF; Meiland HC; Jasper M; de Leeuw WJ; de Knijff P; Sijen T
    Forensic Sci Int Genet; 2009 Sep; 3(4):233-41. PubMed ID: 19647708
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.
    Hollegaard MV; Thorsen P; Norgaard-Pedersen B; Hougaard DM
    Electrophoresis; 2009 Jul; 30(14):2532-5. PubMed ID: 19639574
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-genome amplification of oral rinse self-collected DNA in a population-based case-control study of breast cancer.
    Liang X; Trentham-Dietz A; Titus-Ernstoff L; Newcomb PA; Welch RA; Hutchinson AA; Hampton JM; Sutcliffe CB; Haines JL; Egan KM
    Cancer Epidemiol Biomarkers Prev; 2007 Aug; 16(8):1610-4. PubMed ID: 17684135
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analysis of multiple single nucleotide polymorphisms (SNP) on DNA traces from plasma and dried blood samples.
    Catsburg A; van der Zwet WC; Morré SA; Ouburg S; Vandenbroucke-Grauls CM; Savelkoul PH
    J Immunol Methods; 2007 Apr; 321(1-2):135-41. PubMed ID: 17321541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens.
    Garritsen HS; Fan AX; Bosse N; Hannig H; Kelsch R; Kroll H; Holzgreve W; Zhong XY
    Transfusion; 2009 Feb; 49(2):252-8. PubMed ID: 18980617
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Decreasing amplification bias associated with multiple displacement amplification and short tandem repeat genotyping.
    Ballantyne KN; van Oorschot RA; Muharam I; van Daal A; John Mitchell R
    Anal Biochem; 2007 Sep; 368(2):222-9. PubMed ID: 17583668
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular crowding increases the amplification success of multiple displacement amplification and short tandem repeat genotyping.
    Ballantyne KN; van Oorschot RA; Mitchell RJ; Koukoulas I
    Anal Biochem; 2006 Aug; 355(2):298-303. PubMed ID: 16737679
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of whole-genome amplification of low-copy-number DNA in chimerism analysis after allogeneic stem cell transplantation using STR marker typing.
    Nagy M; Rascon J; Massenkeil G; Ebell W; Roewer L
    Electrophoresis; 2006 Aug; 27(15):3028-37. PubMed ID: 16807933
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Automating sequence-based detection and genotyping of SNPs from diploid samples.
    Stephens M; Sloan JS; Robertson PD; Scheet P; Nickerson DA
    Nat Genet; 2006 Mar; 38(3):375-81. PubMed ID: 16493422
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA quantification of whole genome amplified samples for genotyping on a multiplexed bead array platform.
    Hansen HM; Wiemels JL; Wrensch M; Wiencke JK
    Cancer Epidemiol Biomarkers Prev; 2007 Aug; 16(8):1686-90. PubMed ID: 17684147
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Improved technique that allows the performance of large-scale SNP genotyping on DNA immobilized by FTA technology.
    He H; Argiro L; Dessein H; Chevillard C
    Infect Genet Evol; 2007 Jan; 7(1):128-32. PubMed ID: 16920406
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole genome amplification of DNA extracted from hair samples: potential for use in molecular epidemiologic studies.
    Leanza SM; Burk RD; Rohan TE
    Cancer Detect Prev; 2007; 31(6):480-8. PubMed ID: 18061366
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A low-cost, high-throughput, automated single nucleotide polymorphism assay for forensic human DNA applications.
    Pomeroy R; Duncan G; Sunar-Reeder B; Ortenberg E; Ketchum M; Wasiluk H; Reeder D
    Anal Biochem; 2009 Dec; 395(1):61-7. PubMed ID: 19646946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Optimized DNA extraction to improve reproducibility of short tandem repeat genotyping with highly degraded DNA as target.
    Schmerer WM; Hummel S; Herrmann B
    Electrophoresis; 1999 Jun; 20(8):1712-6. PubMed ID: 10435436
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers.
    Phillips C; Fondevila M; García-Magariños M; Rodriguez A; Salas A; Carracedo A; Lareu MV
    Forensic Sci Int Genet; 2008 Jun; 2(3):198-204. PubMed ID: 19083821
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.