Literature DB >> 14644089

Screening for multiple hereditary hypercoagulability factors using the amplification refractory mutation system.

Berthold Hoppe1, Guido A Heymann, Jürgen Koscielny, Peter Hellstern, Holger Kiesewetter, Abdulgabar Salama.   

Abstract

Many hereditary factors have been implicated in the development of arterial and/or venous thromboembolic diseases. A number of these risk factors can be identified by the amplification refractory mutation system (ARMS). However, the underlying technical conditions for performing ARMS are highly variable, and depend on which risk factors are being analyzed. We have now developed a novel ARMS-based system to simultaneously screen for multiple hypercoagulability factors under identical PCR conditions. This can greatly simplify the process of screening for hereditary hypercoagulability.

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Year:  2003        PMID: 14644089     DOI: 10.1016/j.thromres.2003.08.024

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  6 in total

1.  The association between thrombophilic gene mutations and recurrent pregnancy loss.

Authors:  Ahmad Poursadegh Zonouzi; Nader Chaparzadeh; Saeid Ghorbian; Mahzad Mehrzad Sadaghiani; Laya Farzadi; Alieh Ghasemzadeh; Taiebeh Kafshdooz; Masoud Sakhinia; Ebrahim Sakhinia
Journal:  J Assist Reprod Genet       Date:  2013-08-29       Impact factor: 3.412

2.  Evolving methods for single nucleotide polymorphism detection: Factor V Leiden mutation detection.

Authors:  Herin Oh; Cassandra L Smith
Journal:  J Clin Lab Anal       Date:  2011       Impact factor: 2.352

3.  Polymorphisms in thrombophilic genes are associated with deep venous thromboembolism in an Iranian population.

Authors:  Malak Farajzadeh; Nasrin Bargahi; Ahmad Poursadegh Zonouzi; Davoud Farajzadeh; Nasser Pouladi
Journal:  Meta Gene       Date:  2014-07-15

4.  A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease.

Authors:  Juliane Herm; Berthold Hoppe; Bob Siegerink; Christian H Nolte; Jürgen Koscielny; Karl Georg Haeusler
Journal:  Front Cardiovasc Med       Date:  2017-06-09

5.  Methylenetetrahydrofolate Reductase C677T and A1298C Mutations in Women with Recurrent Spontaneous Abortions in the Northwest of Iran.

Authors:  Ahmad Poursadegh Zonouzi; Nader Chaparzadeh; Mehrdad Asghari Estiar; Mahzad Mehrzad Sadaghiani; Laya Farzadi; Alieh Ghasemzadeh; Masoud Sakhinia; Ebrahim Sakhinia
Journal:  ISRN Obstet Gynecol       Date:  2012-11-14

6.  Prevalence of thrombophilic gene polymorphisms in an azari population of iran.

Authors:  Nasrin Bargahi; Malak Farajzadeh; Ahmad Poursadegh-Zonouzi; Davoud Farajzadeh
Journal:  Hematol Rep       Date:  2014-04-22
  6 in total

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