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Human red blood cell polymorphisms and malaria.

Abstract
Genetic factors are a major determinant of child survival in malaria endemic countries. Identifying which genes are involved and how they affect the malaria disease risk potentially offers a powerful mechanism through which to learn more about the host-parasite relationship. The past few years have seen significant progress towards achieving this goal for some of the best-known malaria resistance genes that determine the structure or function of red blood cells: Gerbich blood group antigen negativity; polymorphisms of the complement receptor genes (most notably CR1); Southeast Asian ovalocytosis; pyruvate kinase deficiency; haemoglobin E; the sickle cell trait; and alpha-thalassaemia are all examples. The challenge for the future must be to translate such advances into fresh approaches to the prevention and treatment of malaria.
AuthorsThomas N Williams
JournalCurrent opinion in microbiology (Curr Opin Microbiol) Vol. 9 Issue 4 Pg. 388-94 (Aug 2006) ISSN: 1369-5274 [Print] England
PMID16815736 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Anion Exchange Protein 1, Erythrocyte
  • Hemoglobin, Sickle
  • Receptors, Complement 3b
  • Viral Envelope Proteins
  • glycoprotein gC, herpes simplex virus type 1
  • Hemoglobin E
Topics
  • Anion Exchange Protein 1, Erythrocyte (genetics)
  • Erythrocytes (metabolism, parasitology)
  • Hemoglobin E (physiology)
  • Hemoglobin, Sickle (physiology)
  • Hemoglobinopathies (genetics)
  • Humans
  • Malaria (genetics, prevention & control)
  • Polymorphism, Genetic
  • Receptors, Complement 3b (genetics)
  • Thalassemia (genetics)
  • Viral Envelope Proteins (genetics)

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