Associated Papers
Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assembly.
Sobh A et al.
The Journal of Allergy and Clinical Immunology, 2016
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib.
Bi LL et al.
Bmc Medical Genetics, 2007
A homozygous Fas ligand gene mutation in a patient causes a new type of autoimmune lymphoproliferative syndrome.
Del-Rey M et al.
Blood, 2006
Separate domains of the human fas ligand dictate self-association and receptor binding.
Orlinick JR et al.
The Journal of Biological Chemistry, 1997
Characterization of Fas (Apo-1, CD95)-Fas ligand interaction.
Schneider P et al.
The Journal of Biological Chemistry, 1997
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