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 *

80 related articles for article (PubMed ID: 19381956)

  • 1. High-throughput mutation screening using a single amplification condition.
    Shi L; Landers JE
    Methods Mol Biol; 2009; 520():195-204. PubMed ID: 19381956
    [TBL] [Abstract][Full Text] [Related]  

  • 2. COLD-PCR: a new platform for highly improved mutation detection in cancer and genetic testing.
    Li J; Makrigiorgos GM
    Biochem Soc Trans; 2009 Apr; 37(Pt 2):427-32. PubMed ID: 19290875
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations.
    Vidal F; Farssac E; Altisent C; Puig L; Gallardo D
    Thromb Haemost; 2001 Apr; 85(4):580-3. PubMed ID: 11341489
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiplex PCR-SSCP for simultaneous screening for mutations in several exons of p53.
    Ozçelik H; Andrulis IL
    Biotechniques; 1995 May; 18(5):742-4. PubMed ID: 7619467
    [No Abstract]   [Full Text] [Related]  

  • 5. Rapid genotyping of factor V Leiden mutation using single-tube bidirectional allele-specific amplification and automated ultrathin-layer agarose gel electrophoresis.
    Sasvari-Szekely M; Gerstner A; Ronai Z; Staub M; Guttman A
    Electrophoresis; 2000 Mar; 21(4):816-21. PubMed ID: 10733227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Optimization of asymmetric polymerase chain reaction for rapid fluorescent DNA sequencing.
    Wilson RK; Chen C; Hood L
    Biotechniques; 1990 Feb; 8(2):184-9. PubMed ID: 2317375
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation screening system for Ehlers-Danlos Syndrome, vascular type by high-resolution melting curve analysis in combination with small amplicon genotyping using genomic DNA.
    Naing BT; Watanabe A; Shimada T
    Biochem Biophys Res Commun; 2011 Feb; 405(3):368-72. PubMed ID: 21219851
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Limited efficiency of universal mini-barcode primers for DNA amplification from desert reptiles, birds and mammals.
    Arif IA; Khan HA; Al Sadoon M; Shobrak M
    Genet Mol Res; 2011 Oct; 10(4):3559-64. PubMed ID: 22057991
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise.
    Bray MS; Boerwinkle E; Doris PA
    Hum Mutat; 2001 Apr; 17(4):296-304. PubMed ID: 11295828
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA) and heteroduplex analysis.
    Crépin M; Escande F; Pigny P; Buisine MP; Calender A; Porchet N; Odou MF;
    Electrophoresis; 2003 Jan; 24(1-2):26-33. PubMed ID: 12652570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-throughput genetic analysis using time-resolved fluorometry and closed-tube detection.
    Nurmi J; Kiviniemi M; Kujanpää M; Sjöroos M; Ilonen J; Lövgren T
    Anal Biochem; 2001 Dec; 299(2):211-7. PubMed ID: 11730345
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Improved sizing of fragile X CCG repeats by nested polymerase chain reaction.
    Levinson G; Maddalena A; Palmer FT; Harton GL; Bick DP; Howard-Peebles PN; Black SH; Schulman JD
    Am J Med Genet; 1994 Jul; 51(4):527-34. PubMed ID: 7943035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detection.
    Larsen LA; Jespersgaard C; Andersen PS
    Nat Protoc; 2007; 2(6):1458-66. PubMed ID: 17545982
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Simple preparation method of PCR fragments for automated DNA sequencing.
    Høgdall E; Boye K; Vuust J
    J Cell Biochem; 1999 Jun; 73(4):433-6. PubMed ID: 10733337
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single-molecule polymerase chain reaction reduces bias: application to DNA methylation analysis by bisulfite sequencing.
    Chhibber A; Schroeder BG
    Anal Biochem; 2008 Jun; 377(1):46-54. PubMed ID: 18358818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Long distance PCR in detection of inversion mutations of F8C gene in hemophilia A patients.
    Poláková H; Zmetáková I; Kádasi L
    Gen Physiol Biophys; 2003 Jun; 22(2):243-53. PubMed ID: 14699993
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A method for the simulation of normal, carrier and affected controls for PCR-RFLP screening of a genetic disease in dairy cattle.
    Mukhopadhyaya PN; Mehta HH; Rathod RN
    Mol Cell Probes; 2000 Dec; 14(6):381-4. PubMed ID: 11090268
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Single nucleotide polymorphism screening with denaturing gradient gel electrophoresis.
    Knapp LA
    Methods Mol Biol; 2009; 578():137-51. PubMed ID: 19768591
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Population-based screening for rare mutations: high-throughput DNA extraction and molecular amplification from Guthrie cards.
    Hamvas A; Trusgnich M; Brice H; Baumgartner J; Hong Y; Nogee LM; Cole FS
    Pediatr Res; 2001 Nov; 50(5):666-8. PubMed ID: 11641464
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.