Literature DB >> 14093913

CHEMICAL CHARACTERIZATION AND SUBUNIT HYBRIDIZATION OF HUMAN HEMOGLOBIN H AND ASSOCIATED COMPOUNDS.

R T JONES, W A SCHROEDER.   

Abstract

Entities:  

Keywords:  BLOOD PROTEIN ELECTROPHORESIS; CHROMATOGRAPHY; EXPERIMENTAL LAB STUDY; HEMOGLOBINS, ABNORMAL; THALASSEMIA; TRYPSIN; ULTRAVIOLET RAYS

Mesh：

Substances：

Year:  1963        PMID： 14093913     DOI： 10.1021/bi00906a031

Source DB:  PubMed          Journal:  Biochemistry        ISSN： 0006-2960            Impact factor:   3.162


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  5 in total

1.  Thalassaemia.

Authors:  E R Huehns
Journal:  Postgrad Med J       Date:  1965-12       Impact factor: 2.401

2.  An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.

Authors:  G D Efremov; R N Wrightstone; T H Huisman; W A Schroeder; C Hyman; J Ortega; K Williams
Journal:  J Clin Invest       Date:  1971-08       Impact factor: 14.808

3.  Haemoglobin H disease in Arabs in Kuwait.

Authors:  S A Ali
Journal:  J Clin Pathol       Date:  1969-03       Impact factor: 3.411

4.  Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

Authors:  D Housman; B G Forget; A Skoultchi; E J Benz
Journal:  Proc Natl Acad Sci U S A       Date:  1973-06       Impact factor: 11.205

5.  Human embryonic, fetal, and adult hemoglobins have different subunit interface strengths. Correlation with lifespan in the red cell.

Authors:  Lois R Manning; J Eric Russell; Julio C Padovan; Brian T Chait; Anthony Popowicz; Robert S Manning; James M Manning
Journal:  Protein Sci       Date:  2007-08       Impact factor: 6.725
  5 in total

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