Literature DB >> 12406100

Rapid detection of the major Mediterranean beta-thalassaemia mutations by real-time polymerase chain reaction using fluorophore-labelled hybridization probes.

Isabel Moreno1, Pascual Bolufer, M Luz Perez, Eva Barragán, Miguel A Sanz.   

Abstract

We present a new method to detect the major beta-thalassaemia mutations of the Mediterranean countries (IVS I-1, IVS I-6, IVS I-110, CD-37 and CD-39). The procedure is based upon real-time polymerase chain reaction (PCR), using specific fluorescently labelled hybridization probes. The melting curves for each of the specific probes obtained after PCR enabled the identification of different alleles. Genotyping of 71 patients with thalassaemia and 20 controls without thalassaemia by the established method and conventional allele-specific restriction enzyme analysis produced identical results. The established method is a robust, fast and straightforward assay that allows detection of the major Mediterranean beta-thalassaemia mutations simultaneously in less than 60 min.

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Year:  2002        PMID: 12406100     DOI: 10.1046/j.1365-2141.2002.03823.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  5 in total

1.  A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contamination.

Authors:  Catherine Costa; Serge Pissard; Emmanuelle Girodon; Danièle Huot; Michel Goossens
Journal:  Mol Diagn       Date:  2003

2.  Real-time PCR genotyping using displacing probes.

Authors:  Jinping Cheng; Yongyou Zhang; Qingge Li
Journal:  Nucleic Acids Res       Date:  2004-04-15       Impact factor: 16.971

3.  beta-Thalassaemia Major in a Spanish Patient due to a Compound Heterozygosity for CD39 C --> T/-28 A --> C.

Authors:  Soledad Gamarra; Guillermo Garcia-Effron; Carmen Monteserin; Isabel Lopez-Villar; Florinda Gilsanz; Joaquín Martinez-Lopez
Journal:  Adv Hematol       Date:  2009-07-28

4.  Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations.

Authors:  Chia-Cheng Hung; Yi-Ning Su; Chia-Yun Lin; Yin-Fei Chang; Chien-Hui Chang; Wen-Fang Cheng; Chi-An Chen; Chien-Nan Lee; Win-Li Lin
Journal:  BMC Biotechnol       Date:  2008-08-12       Impact factor: 2.563

5.  2. Post-Natal Molecular Diagnosis of Inherited Diseases.

Authors:  Maurizio Ferrari; Laura Cremonesi; Stefania Stenirri
Journal:  EJIFCC       Date:  2008-04-03
  5 in total

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