Literature DB >> 14311973

A NEW HAEMOGLOBIN, D IBADAN (BETA-87 THREONINE -- LYSINE), PRODUCING NO SICKLE-CELL HAEMOGLOBIN D DISEASE WITH HAEMOGLOBIN S.

E J WATSON-WILLIAMS, D BEALE, D IRVINE, H LEHMANN.   

Abstract

Entities:  

Keywords:  ANEMIA, SICKLE CELL; CHROMATOGRAPHY; ELECTROPHORESIS; GENETICS, HUMAN; HEMOGLOBINS, ABNORMAL; LYSINE; NIGERIA; THREONINE

Mesh：

Substances：

Year:  1965        PMID： 14311973     DOI： 10.1038/2051273a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  14 in total

1.  A NEW HAEMOGLOBIN IN A THAI FAMILY. A CASE OF HAEMOGLOBIN SIRIRAJ-BETA THALASSAEMIA.

Authors:  S TUCHINDA; D BEALE; H LEHMANN
Journal:  Br Med J       Date:  1965-06-19

Review 2.  Haemoglobin D Punjab (D Los Angeles).

Authors:  F Vella; H Lehmann
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

3.  [Occureence and heterogeneity of abnormal haemoglobins and thalassemia syndromes in the German population (author's transl)].

Authors:  E Kohne; E Kleihauer
Journal:  Klin Wochenschr       Date:  1974-11-01

Review 4.  Molecular basis of hereditary disease.

Authors:  H Harris
Journal:  Br Med J       Date:  1968-04-20

5.  Aseptic necrosis of the femoral head in a white boy with S-D hemoglobinopathy.

Authors:  T L Slovis; J O Haller; W E Berdon; D H Baker
Journal:  Pediatr Radiol       Date:  1973-12

6.  Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S.

Authors:  F I Konotey-Ahulu; J L Kinderlerer; H Lehmann; B Ringelhann
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

7.  The amino acid substitution and some chemical properties of a variant human erythrocyte carbonic anhydrase: carbonic anhydrase Id-Michigan.

Authors:  T B Shows
Journal:  Biochem Genet       Date:  1967-09       Impact factor: 1.890

8.  Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem.

Authors:  F I Konotey-Ahulu; E Gallo; H Lehmann; B Ringelhann
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

9.  The suppression of haemoglobin E synthesis when hemoglobin H disease and hemoglobin E trait occur together.

Authors:  S Tuchinda; D Beale; H Lehman
Journal:  Humangenetik       Date:  1967

Review 10.  Hemoglobin variants: biochemical properties and clinical correlates.

Authors:  Christopher S Thom; Claire F Dickson; David A Gell; Mitchell J Weiss
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915
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