Literature DB >> 4855313

Unbalanced globin chain synthesis in reticulocytes of sickle cell trait individuals with low concentrations of hemoglobin S.

J DeSimone, L Kleve, M A Longley, J Shaeffer.   

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Year:  1974        PMID： 4855313     DOI： 10.1016/s0006-291x(74)80017-3

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


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  5 in total

1.  A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.

Authors:  T H Huisman; A Miller; W A Schroeder
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025

2.  Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.

Authors:  J R Shaeffer; J DeSimone; L J Kleve
Journal:  Biochem Genet       Date:  1975-12       Impact factor: 1.890

3.  beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].

Authors:  J G Adams; M H Steinberg; M V Newman; W T Morrison; E J Benz; R Iyer
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

4.  Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.

Authors:  A E Felice; R Ozdonmez; M E Headlee; T H Huisman
Journal:  Biochem Genet       Date:  1982-08       Impact factor: 1.890

5.  Modification of hemoglobin H disease by sickle trait.

Authors:  K K Matthay; W C Mentzer; A M Dozy; Y W Kan; D F Bainton
Journal:  J Clin Invest       Date:  1979-10       Impact factor: 14.808
  5 in total

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