Literature DB >> 6278929

Thalassemia: recent insights into molecular mechanisms.

M H Steinberg, J G Adams.   

Abstract

Recent advances in defining the molecular basis for the thalassemia syndromes are discussed. We now realize that the causes of the thalassemia phenotype are diverse and include gene deletions, nuclear RNA processing defects, nonsense mutations, fusion genes, termination codon mutants, and unstable globin chains.

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Year:  1982        PMID: 6278929     DOI: 10.1002/ajh.2830120113

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  3 in total

1.  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

2.  Disruption of the Hbs1l-Myb locus causes hereditary persistence of fetal hemoglobin in a mouse model.

Authors:  Mikiko Suzuki; Hiromi Yamazaki; Harumi Y Mukai; Hozumi Motohashi; Lihong Shi; Osamu Tanabe; James Douglas Engel; Masayuki Yamamoto
Journal:  Mol Cell Biol       Date:  2013-02-19       Impact factor: 4.272

Review 3.  Thalassemic hemoglobinopathies.

Authors:  M H Steinberg; J G Adams
Journal:  Am J Pathol       Date:  1983-12       Impact factor: 4.307

  3 in total

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