BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 1301951)

  • 1. A modified approach to identification of the sickle cell anemia mutation by means of allele-specific polymerase chain reaction.
    Birikh KR; Plutalov OV; Schwartz EI; Devi PS; Berlin YA
    Hum Mutat; 1992; 1(5):417-9. PubMed ID: 1301951
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of the sickle-cell anemia mutation by means of the PCR-mediated mismatch-dependent primer extension.
    Birikh KR; Plutalov OV; Schwartz EI; Berlin YuA
    Nucleic Acids Symp Ser; 1991; (24):317. PubMed ID: 1841370
    [No Abstract]   [Full Text] [Related]  

  • 3. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
    Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sequence of the -530 region of the beta-globin gene of sickle cell anemia patients with the Arabian haplotype.
    Zeng FY; Rodgers GP; Huang SZ; Schechter AN; Salamah M; Perrine S; Berg PE
    Hum Mutat; 1994; 3(2):163-5. PubMed ID: 8199597
    [No Abstract]   [Full Text] [Related]  

  • 5. [Detection of sickle cell gene by analysis of amplified DNA sequences].
    Huang SZ; Sheng M; Zhao JQ; Qiu XK; Zeng YT; Wang QS; He MX; Zhu JM; Liu WP; Li WW
    Yi Chuan Xue Bao; 1989; 16(6):475-82. PubMed ID: 2640144
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of sickle cell gene using polymerase chain reaction & restriction enzyme Bsu 361.
    Husain SM; Kalavathi P; Anandaraj MP
    Indian J Med Res; 1995 Jun; 101():273-6. PubMed ID: 7672839
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of Iranian families with sickle cell disease.
    Ayatollahi M; Zakerinia M; Haghshenas M
    J Trop Pediatr; 2005 Jun; 51(3):136-40. PubMed ID: 15831669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of unusual hemoglobinopathies.
    Kim JH; Lebo RV; Cai SP; Su X; Chung JH; Mentzer WC; Golbus MS
    Am J Med Genet; 1994 Mar; 50(1):15-20. PubMed ID: 8160747
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular exclusion of haemoglobin SD disease by prenatal diagnosis.
    Fodor FH; Eng CM
    Prenat Diagn; 1999 Jan; 19(1):58-60. PubMed ID: 10073909
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An alternate nonisotopic technique of PCR-mediated allele-specific oligonucleotide analysis for the detection of a point mutation.
    Nakajima H; Hamaguchi T; Tomita K; Uenaka R; Yamagata K; Hanafusa T; Kuwajima M; Noguchi T; Tanaka T; Kono N
    Res Commun Chem Pathol Pharmacol; 1993 Jan; 79(1):3-10. PubMed ID: 8434131
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM; El-Khatib FF; Ayesh S
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC.
    Su YN; Lee CN; Hung CC; Chen CA; Cheng WF; Tsao PN; Yu CL; Hsieh FJ
    Hum Mutat; 2003 Oct; 22(4):326-36. PubMed ID: 12955718
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of mutations using microarrays of poly(C)10-poly(T)10 modified DNA probes immobilized on agarose films.
    Dufva M; Petersen J; Stoltenborg M; Birgens H; Christensen CB
    Anal Biochem; 2006 May; 352(2):188-97. PubMed ID: 16615930
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia.
    Foglieni B; Galbiati S; Ferrari M; Cremonesi L
    Methods Mol Biol; 2008; 444():169-82. PubMed ID: 18425480
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA; Wering ME; Luo HY; Basran RK; Steinberg MH; Smith HP; Chui DH
    Eur J Haematol; 2007 Jan; 78(1):82-5. PubMed ID: 17038017
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development of a PCR/ligase detection reaction/nanogold-based universal array approach for the detection of low-abundant DNA point mutations.
    Yi P; Lu W; Guo J; Liu Q; Chen Z; Han J; Li L
    Cell Biochem Biophys; 2011 Dec; 61(3):629-36. PubMed ID: 21847634
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homogeneity of beta(0)-thalassemia codon 17 (A-->T) alleles in Northern Thailand using a direct DNA sequencing method.
    Sanguansermsri P; Shimbhu D; Wongvilairat R; Saetung R; Sanguansermsri T
    J Med Assoc Thai; 2004 Aug; 87(8):883-6. PubMed ID: 15471290
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA.
    Kobayashi M; Rappaport E; Blasband A; Semeraro A; Sartore M; Surrey S; Fortina P
    Mol Cell Probes; 1995 Jun; 9(3):175-82. PubMed ID: 7477010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P; Flierl A; Kottlors M; Reichmann H
    Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel diagnostic test detects a low frequency of the hemicentin Gln5345Arg variant among Northern Irish age related macular degeneration patients.
    McKay GJ; Clarke S; Hughes A; McConnell V; Schultz DW; Klein ML; Silvestri G; Simpson DA
    Mol Vis; 2004 Sep; 10():682-7. PubMed ID: 15467524
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.