Literature DB >> 1248825

Is haemoglobin G alpha Philadelphia linked to alpha-thalassaemia?

C Politis-Tsegos, A Lang, R Stathopoulou, H Lehmann.   

Abstract

The question, "Is Hb G alpha Philadelphia linked to alpha-thalassaemia?" was first posed because the abnormal haemoglobin is found in heterozygotes at a concentration greater than 25%, the proportion predicted from a 4 alpha-chain gene model. Globin chain biosynthesis was studied in a West Indian family in which one parent had beta + thalassaemia and the other was heterozygous for the G alpha Philadelphia chain gene. The former had a globin chain production ratio alpha/beta well above 1, while the latter had a ratio significantly less than 1. One child of the marriage had inherited the beta + thalassaemia from one parent and the G alpha Philadelphia chain gene from the other and showed the typical picture of alpha/beta-thalassaemia (alpha/beta ratio slightly above normal). It is explained in the discussion that the evidence favours a close linkage of 2 alpha-chain genes.

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Year:  1976        PMID: 1248825     DOI: 10.1007/bf00270401

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  25 in total

Review 1.  Hemoglobin Constant Spring, and unusual alpha-chain variant involved in the etiology of hemoglobin H disease.

Authors:  J B Clegg; D J Weatherall
Journal:  Ann N Y Acad Sci       Date:  1974       Impact factor: 5.691

2.  Multiple alpha chain loci for human haemoglobins: Hb J-Buda and Hb G-Pest.

Authors:  S R Hollán; J G Szelenyi; G Brimhall; M Duerst; R T Jones; R D Koler; Z Stocklen
Journal:  Nature       Date:  1972-01-07       Impact factor: 49.962

Review 3.  Duplication of structural genes for hemoglobin alpha and beta chains in man.

Authors:  D L Rucknagel; W P Winter
Journal:  Ann N Y Acad Sci       Date:  1974-11-29       Impact factor: 5.691

4.  The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.

Authors:  S Ottolenghi; W G Lanyon; J Paul; R Williamson; D J Weatherall; J B Clegg; J Pritchard; S Pootrakul; W H Boon
Journal:  Nature       Date:  1974-10-04       Impact factor: 49.962

5.  Different types of alpha-thalassaemia and significance of haemoglobin Bart's in neonates.

Authors:  H Lehmann
Journal:  Lancet       Date:  1970-07-11       Impact factor: 79.321

6.  Hb K Woolwich the cause of a thalassaemia.

Authors:  A Lang; H Lehmann; P A King-Lewis
Journal:  Nature       Date:  1974-05-31       Impact factor: 49.962

7.  The clinical and biosynthetic characterization of -thalassaemia.

Authors:  H H Knox-Macaulay; D J Weatherall; J B Clegg; J Bradley; M J Brown
Journal:  Br J Haematol       Date:  1972-04       Impact factor: 6.998

8.  Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.

Authors:  T H Huisman; A M Dozy
Journal:  J Chromatogr       Date:  1965-07

Review 9.  Multiple hemoglobin alpha-chain loci in monkeys, apes, and man.

Authors:  P E Nute
Journal:  Ann N Y Acad Sci       Date:  1974-11-29       Impact factor: 5.691

10.  Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene.

Authors:  H Lehmann; R W Carrell
Journal:  Br Med J       Date:  1968-12-21
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  2 in total

1.  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

2.  Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.

Authors:  A E Felice; B B Webber; T H Huisman
Journal:  Biochem Genet       Date:  1981-06       Impact factor: 1.890

  2 in total

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