[Lymphoproliferative disorders caused by hereditary genetic defects]

Nihon Rinsho Meneki Gakkai Kaishi. 2003 Dec;26(6):311-22.

[Article in Japanese]

Authors

Hirokazu Kanegane¹, Toshio Miyawaki

Affiliation

¹ Department of Pediatrics, Faculty of Medicine, Toyama Medical and Pharmaceutical University.

PMID: 14752931

No abstract available

Publication types

Review

MeSH terms

Animals
Apoptosis
Autoimmune Diseases*
Carrier Proteins / genetics*
Fas Ligand Protein
Genetic Diseases, Inborn / complications*
Genetic Linkage
Humans
Intracellular Signaling Peptides and Proteins*
Lymphoproliferative Disorders / etiology*
Lymphoproliferative Disorders / genetics*
Lymphoproliferative Disorders / immunology
Membrane Glycoproteins / genetics
Mice
Signaling Lymphocytic Activation Molecule Associated Protein
X Chromosome

Substances

Carrier Proteins
FASLG protein, human
Fas Ligand Protein
Fasl protein, mouse
Intracellular Signaling Peptides and Proteins
Membrane Glycoproteins
SH2D1A protein, human
Sh2d1a protein, mouse
Signaling Lymphocytic Activation Molecule Associated Protein