Literature DB >> 8144356

A novel 13 Bp deletion in the 3'UTR of the beta-globin gene causes beta-thalassemia in a Turkish patient.

A N Başak1, A Ozer, B Kirdar, N Akar.   

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Year:  1993        PMID： 8144356     DOI： 10.3109/03630269309043496

Source DB:  PubMed          Journal:  Hemoglobin        ISSN： 0363-0269            Impact factor:   0.849


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  4 in total

1.  A nucleolin-binding 3' untranslated region element stabilizes beta-globin mRNA in vivo.

Authors:  Yong Jiang; Xiang-Sheng Xu; J Eric Russell
Journal:  Mol Cell Biol       Date:  2006-03       Impact factor: 4.272

Review 2.  A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants.

Authors:  Jian-Min Chen; Claude Férec; David N Cooper
Journal:  Hum Genet       Date:  2006-06-29       Impact factor: 4.132

3.  Structural and functional analysis of an mRNP complex that mediates the high stability of human beta-globin mRNA.

Authors:  J Yu; J E Russell
Journal:  Mol Cell Biol       Date:  2001-09       Impact factor: 4.272

4.  Premarital Genetic Diagnosis Revealed Co-heredity Nature of Beta Globin Gene 25-26 del AA and 3'UTR+101 G-C Variants in Two Beta Thalassemia Heterozygotes.

Authors:  Kanay Yararbaş; Yasemin Ardıçoğlu; Nejat Akar
Journal:  Turk J Haematol       Date:  2016-10-18       Impact factor: 1.831
  4 in total

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