Literature DB >> 5086396

Hemoglobin Lepore trait: globin synthesis in bone marrow and peripheral blood.

F Gill, J Atwater, E Schwartz.   

Abstract

There was decreased synthesis of the beta-globin chain in the peripheral blood, and equal synthesis of alpha- and non-alpha-chains in the bone marrow of three patients with hemoglobin Lepore trait, similar to the findings in patients with heterozygous beta-thalassemia. There is a relative instability of the synthetic mechanism for normal beta-chain in these patients.

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Year:  1972        PMID: 5086396     DOI: 10.1126/science.178.4061.623

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  4 in total

1.  Imbalance in alpha and beta globin synthesis associated with a hemoglobinopathy.

Authors:  R F Rieder; G W James
Journal:  J Clin Invest       Date:  1974-10       Impact factor: 14.808

Review 2.  The thalassemias: molecular mechanisms of human genetic disease.

Authors:  R A Spritz; B G Forget
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

3.  Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.

Authors:  A W Nienhuis; P H Canfield; W F Anderson
Journal:  J Clin Invest       Date:  1973-07       Impact factor: 14.808

4.  Free alpha-globin pool in human bone marrow.

Authors:  F M Gill; E Schwartz
Journal:  J Clin Invest       Date:  1973-12       Impact factor: 14.808

  4 in total

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