Genetic analysis of integrin function in man: LAD-1 and other syndromes

This publication has 70 references indexed in Scilit:

• Model building by comparison at CASP3: Using expert knowledge and computer automation
  Proteins-Structure Function and Bioinformatics, 1999
• The dermal—epidermal junction
  Current Opinion in Cell Biology, 1997
• Lymphocyte Homing and Homeostasis
  Science, 1996
• β2 (CD18) Mutations Abolish Ligand Recognition by I Domain Integrins LFA-1 ( αLβ2, CD11a/CD18) and MAC-1 ( αMβ2, CD11b/CD18)
  Published by Elsevier ,1995
• Ligand and cation binding are dual functions of a discrete segment of the integrin β3 subunit: Cation displacement is involved in ligand binding
  Cell, 1994
• Ser-752-->Pro mutation in the cytoplasmic domain of integrin beta 3 subunit and defective activation of platelet integrin alpha IIb beta 3 (glycoprotein IIb-IIIa) in a variant of Glanzmann thrombasthenia.
  Proceedings of the National Academy of Sciences, 1992
• Molecular basis for a severe case of leukocyte adhesion deficiency
  European Journal of Immunology, 1992
• Localization of an Arg-Gly-Asp Recognition Site Within an Integrin Adhesion Receptor
  Science, 1988
• LEUKOCYTE ADHESION DEFICIENCY: An Inherited Defect in the Mac-1, LFA-1, and p150,95 Glycoproteins
  Annual Review of Medicine, 1987
• The Severe and Moderate Phenotypes of Heritable Mac-1, LFA-1 Deficiency: Their Quantitative Definition and Relation to Leukocyte Dysfunction and Clinical Features
  The Journal of Infectious Diseases, 1985