Literature DB >> 5923474

Hemoglobin C trait in Saskatchewan.

F Vella.   

Abstract

In the beta chain of normal adult hemoglobin, the amino acid residues in positions six and seven are glutamic acid. In hemoglobin C, lysine replaces the glutamic acid residue in position six. Two hemoglobin variants have been described in which lysine replaces the glutamic acid residue in position seven.During a search for abnormalities of hemoglobin synthesis detectable by conventional electrophoretic techniques, some 20,000 blood samples were screened from the population of Saskatchewan. Two specimens gave an electrophoretic pattern of hemoglobins A and C. The abnormal hemoglobin was purified and "finger printed" and found to be the same as classical hemoglobin C (i.e. alpha(2)beta(2) 6 glu --> lys). Both specimens had originated from healthy blood donors, one a Ghanaian student and the other a young white man of immigrant Irish-Scottish parents living near Saskatoon.

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Year:  1966        PMID: 5923474      PMCID: PMC1935820     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  16 in total

1.  Homozygous haemoglobin-C disease in a white family with special reference to blood autolysis studies.

Authors:  S M LEWIS; C G ANDERSON; E BASKIND
Journal:  Br J Haematol       Date:  1957-01       Impact factor: 6.998

2.  Malaria in carriers of the sickle-cell trait and in newborn children.

Authors:  A C ALLISON
Journal:  Exp Parasitol       Date:  1957-07       Impact factor: 2.011

3.  Haemoglobin Norfolk: a new haemoglobin found in an English family with observations on the naming of new haemoglobin variants.

Authors:  J A AGER; H LEHMANN; F VELLA
Journal:  Br Med J       Date:  1958-08-30

4.  [Association by electrophoresis of a thalassemic syndrome and an unidentified abnormal hemoglobin in a Frenchman from Picardy; examination by electron microscopy].

Authors:  R ANDRE; M BESSIS; B DREYFUS; S JACOB; R MALASSENET
Journal:  Rev Hematol       Date:  1958 Jan-Mar

5.  Intraerythrocytic crystals in a white patient with hemoglobin C in the absence of other types of hemoglobin.

Authors:  L W DIGGS; A P KRAUS; D B MORRISON; R P RUDNICKI
Journal:  Blood       Date:  1954-12       Impact factor: 22.113

6.  Solubilities of naturally occurring mixtures of human hemoglobin.

Authors:  H A ITANO
Journal:  Arch Biochem Biophys       Date:  1953-11       Impact factor: 4.013

7.  A new inherited abnormality of human hemoglobin.

Authors:  H A ITANO; J V NEEL
Journal:  Proc Natl Acad Sci U S A       Date:  1950-11       Impact factor: 11.205

8.  [Hemoglobin C in Europeans: 1 new, probable homozygote and 3 heterozygote carriers of the anomaly].

Authors:  H R Marti; H Lehmann; G Keiser; W Siegenthaler
Journal:  Blut       Date:  1965-09

9.  Hemoglobin C Harlem: a sickling variant containing amino acid substitutions in two residues of the beta-polypeptide chain.

Authors:  R M Bookchin; R L Nagel; H M Ranney; A S Jacobs
Journal:  Biochem Biophys Res Commun       Date:  1966-04-19       Impact factor: 3.575

10.  A new haemoglobin, J Toronto (alpha-5 alanine to aspartic acid).

Authors:  J H Crookston; D Irvine; D Beale; H Lehmann
Journal:  Nature       Date:  1965-12-11       Impact factor: 49.962

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