Literature DB >> 10222362

Rapid detection of prothrombotic mutations of prothrombin (G20210A), factor V (G1691A), and methylenetetrahydrofolate reductase (C677T) by real-time fluorescence PCR with the LightCycler.

N von Ahsen1, E Schütz, V W Armstrong, M Oellerich.   

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Year:  1999        PMID: 10222362

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


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  14 in total

1.  Portal vein thrombosis following percutaneous transhepatic cholangiography-An unusual presentation of Prothrombin (Factor II) gene mutation.

Authors:  Ian M Brennan; Muneeb Ahmed
Journal:  World J Radiol       Date:  2012-05-28

2.  Genotyping of single nucleotide substitutions.

Authors:  Cyril D S Mamotte
Journal:  Clin Biochem Rev       Date:  2006-02

3.  Prevalence of the prothrombin G20210A polymorphism in the Lebanese population: use of a reverse hybridization strip assay approach.

Authors:  Amira S Sabbagh; Georges Ibrahim; Ziad Kanaan; Dina M R Shammaa; Rabab Abdel Khalek; Mona Ghasham; Layal Greige; Rami A R Mahfouz
Journal:  Mol Biol Rep       Date:  2007-12-08       Impact factor: 2.316

4.  Rapid genotyping for most common TGFBI mutations with real-time polymerase chain reaction.

Authors:  Shigeo Yoshida; Yoko Yamaji; Ayako Yoshida; Yoshihiro Noda; Yuji Kumano; Tatsuro Ishibashi
Journal:  Hum Genet       Date:  2005-03-03       Impact factor: 4.132

5.  Rapid Screening for Deleted Form of β-thalassemia by Real-Time Quantitative PCR.

Authors:  Liang-Yin Ke; Jan-Gowth Chang; Chao-Sung Chang; Li-Ling Hsieh; Ta-Chih Liu
Journal:  J Clin Lab Anal       Date:  2016-08-16       Impact factor: 2.352

6.  Hemochromatosis and transferrin receptor gene polymorphisms in chronic hepatitis C: impact on iron status, liver injury and HCV genotype.

Authors:  Sven G Gehrke; Wolfgang Stremmel; Inge Mathes; Hans-Dieter Riedel; Karin Bents; Birgit Kallinowski
Journal:  J Mol Med (Berl)       Date:  2003-10-14       Impact factor: 4.599

7.  Multiplex assay for genetic testing of thrombophilia: a method for routine clinical care.

Authors:  Mónica López; Pilar Giraldo; Patricia Alvarez; R Cornudella; Miguel Pocoví; Antonio Martínez; Jordi Fontcuberta; José Manuel Soria
Journal:  J Clin Lab Anal       Date:  2007       Impact factor: 2.352

8.  Analysis of common mutations in the galactose-1-phosphate uridyl transferase gene: new assays to increase the sensitivity and specificity of newborn screening for galactosemia.

Authors:  Steven F Dobrowolski; Richard A Banas; Joseph G Suzow; Michelle Berkley; Edwin W Naylor
Journal:  J Mol Diagn       Date:  2003-02       Impact factor: 5.568

9.  Vitamin B12 level in peripheral arterial disease.

Authors:  Katalin S Zsóri; Zoltán Csiki; Éva Katona; Zsuzsnna Bereczky; Amir-Houshang Shemirani
Journal:  J Thromb Thrombolysis       Date:  2013-07       Impact factor: 2.300

10.  Prothrombin gene G20210A mutation in acute deep venous thrombosis patients with poor response to warfarin therapy.

Authors:  F M Attia; D P Mikhailidis; S A Reffat
Journal:  Open Cardiovasc Med J       Date:  2009-10-21
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