BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 9798659)

  • 1. Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutations.
    Ugozzoli LA; Lowery JD; Reyes AA; Lin CI; Re A; Locati F; Galanello R; Macioni L; Maggio A; Giambona A; Loutradi A; Boussiou M; Wallace RB
    Am J Hematol; 1998 Nov; 59(3):214-22. PubMed ID: 9798659
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of four beta-thalassemia point mutations in Iranians using a PCR-ELISA genotyping system.
    Gill P; Forouzandeh M; Eshraghi N; Ghalami M; Safa M; Noori-Daloii MR
    Mol Cell Probes; 2008 Apr; 22(2):103-9. PubMed ID: 18036776
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.
    Naja RP; Kaspar H; Shbaklo H; Chakar N; Makhoul NJ; Zalloua PA
    Am J Hematol; 2004 Apr; 75(4):220-4. PubMed ID: 15054814
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A new method of nonradioactive labelling of oligonucleotides and their use as allele-specific probes for detecting mutations causing beta-thalassemia].
    Lebedeva IV; Ivanovskaia MG; Fedorov AN; Limborskaia SA; Shabarova ZA
    Mol Biol (Mosk); 1994; 28(4):796-804. PubMed ID: 7990807
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily.
    Maggio A; Giambona A; Cai SP; Wall J; Kan YW; Chehab FF
    Blood; 1993 Jan; 81(1):239-42. PubMed ID: 8417793
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis for beta-thalassemia syndromes using HRP-labeled oligonucleotide probes at Siriraj Hospital.
    Winichagoon P; Fucharoen S; Siritanaratkul N; Tassana P; Thonglairoam V; Siriboon W; Kanokpongsakdi S
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():282-6. PubMed ID: 8629125
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nonisotopic detection of human papillomavirus DNA in clinical specimens using a consensus PCR and a generic probe mix in an enzyme-linked immunosorbent assay format.
    Kornegay JR; Shepard AP; Hankins C; Franco E; Lapointe N; Richardson H; Coutleé F;
    J Clin Microbiol; 2001 Oct; 39(10):3530-6. PubMed ID: 11574568
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.
    Wang W; Kham SK; Yeo GH; Quah TC; Chong SS
    Clin Chem; 2003 Feb; 49(2):209-18. PubMed ID: 12560342
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients.
    Honardoost MA; Tabatabaeian H; Akbari M; Salehi M
    Gene; 2014 Oct; 549(1):1-6. PubMed ID: 24946023
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma.
    Li Y; Di Naro E; Vitucci A; Zimmermann B; Holzgreve W; Hahn S
    JAMA; 2005 Feb; 293(7):843-9. PubMed ID: 15713774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Beta-thalassemia mutations in Singapore--a strategy for prenatal diagnosis.
    Ng IS; Ong JB; Tan CL; Law HY
    Hum Genet; 1994 Oct; 94(4):385-8. PubMed ID: 7927334
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of beta-thalassemia mutations by ASO hybridization of PCR amplified DNA with digoxigenin ddUTP labeled oligonucleotides.
    Efremov DG; Dimovski AJ; Efremov GD
    Hemoglobin; 1991; 15(6):525-33. PubMed ID: 1814858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Utility of the polymerase chain reaction (PCR) for prenatal diagnosis of genetic disease.
    Lindeman R; Wallace R; Volpato F; Hu SP; Trent RJ
    Pathology; 1991 Apr; 23(2):158-63. PubMed ID: 1745568
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Development and evaluation of a reverse dot blot assay for the simultaneous detection of common alpha and beta thalassemia in Chinese.
    Lin M; Zhu JJ; Wang Q; Xie LX; Lu M; Wang JL; Wang CF; Zhong TY; Zheng L; Pan MC; Wu JR; Wen YF; Liu GR; Zhan XF; Lin F; Yang LY
    Blood Cells Mol Dis; 2012 Feb; 48(2):86-90. PubMed ID: 22197394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W; Schleiemacher E; Panich V; Nopparatana C; Saechan V; Laosombat V; Pornpatkul M; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotyping of β-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
    Durmaz B; Ozkinay F; Onay H; Karaca E; Aydinok Y; Tavmergen E; Vrettou C; Traeger-Synodinos J; Kanavakis E
    Hemoglobin; 2012; 36(3):230-43. PubMed ID: 22524255
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes.
    Saiki RK; Walsh PS; Levenson CH; Erlich HA
    Proc Natl Acad Sci U S A; 1989 Aug; 86(16):6230-4. PubMed ID: 2762325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Improvement of detection of paternally inherited fetal mutant genes for β-globin in maternal plasma by PNA clamp].
    Huang K; Pan HF
    Zhonghua Xue Ye Xue Za Zhi; 2013 Mar; 34(3):233-6. PubMed ID: 23683423
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lateral flow dipstick test for genotyping of 15 beta-globin gene (HBB) mutations with naked-eye detection.
    Papanikos F; Iliadi A; Petropoulou M; Ioannou PC; Christopoulos TK; Kanavakis E; Traeger-Synodinos J
    Anal Chim Acta; 2012 May; 727():61-6. PubMed ID: 22541824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations.
    Teh LK; Lee TY; Tan JA; Lai MI; George E
    Int J Lab Hematol; 2015 Feb; 37(1):79-89. PubMed ID: 24725998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.