Literature DB >> 12871427

Budd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin gene.

Z Balim, B Kosova, K Falzon, S Bezzina Wettinger, Y Colak.   

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Year:  2003        PMID： 12871427     DOI： 10.1046/j.1538-7836.2003.t01-2-00115.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  5 in total

Review 1.  A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overview.

Authors:  Jian-Min Chen; Claude Férec; David N Cooper
Journal:  Hum Genet       Date:  2006-04-28       Impact factor: 4.132

Review 2.  3' end mRNA processing: molecular mechanisms and implications for health and disease.

Authors:  Sven Danckwardt; Matthias W Hentze; Andreas E Kulozik
Journal:  EMBO J       Date:  2008-02-06       Impact factor: 11.598

3.  The 3' end prothrombin gene variants in serbian patients with idiopathic thrombophilia.

Authors:  M Aradjanski; V Djordjevic; I Pruner; B Tomic; M Gvozdenov; M Kovac; D Radojkovic
Journal:  Balkan J Med Genet       Date:  2015-04-10       Impact factor: 0.519

Review 4.  Processing and transcriptome expansion at the mRNA 3' end in health and disease: finding the right end.

Authors:  Anton Ogorodnikov; Yulia Kargapolova; Sven Danckwardt
Journal:  Pflugers Arch       Date:  2016-05-25       Impact factor: 3.657

Review 5.  Emerging Roles of RNA 3'-end Cleavage and Polyadenylation in Pathogenesis, Diagnosis and Therapy of Human Disorders.

Authors:  Jamie Nourse; Stefano Spada; Sven Danckwardt
Journal:  Biomolecules       Date:  2020-06-17
  5 in total

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