×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
GeneticVariation
disease
CLINVAR
×
Entrez Id:
356
Gene Symbol:
FASLG
FASLG
0.890
Biomarker
disease
CTD_human
×
Entrez Id:
841
Gene Symbol:
CASP8
CASP8
0.330
Biomarker
disease
CTD_human
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Spontaneous murine lupus-like syndromes. Clinical and immunopathological manifestations in several strains.
309911
1978
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Distribution of lymphocytes identified by surface markers in murine strains with systemic lupus erythematosus-like syndromes.
762500
1979
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Splenic immunoglobulin-secreting cells and their regulation in autoimmune mice.
6444324
1980
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Deficient interleukin 2 activity in MRL/Mp and C57BL/6J mice bearing the lpr gene.
6975351
1981
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Dissociation of severe lupus-like disease from polyclonal B cell activation and IL 2 deficiency in C3H-lpr/lpr mice.
6610701
1984
×
Entrez Id:
356
Gene Symbol:
FASLG
FASLG
0.890
Biomarker
disease
MGD
A new mutation, gld, that produces lymphoproliferation and autoimmunity in C3H/HeJ mice.
6693832
1984
×
Entrez Id:
356
Gene Symbol:
FASLG
FASLG
0.890
Biomarker
disease
MGD
Immunologic abnormalities of mice bearing the gld mutation suggest a common pathway for murine nonmalignant lymphoproliferative disorders with autoimmunity.
3856256
1985
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Phenotypic, functional, and molecular genetic comparisons of the abnormal lymphoid cells of C3H-lpr/lpr and C3H-gld/gld mice.
3009614
1986
×
Entrez Id:
356
Gene Symbol:
FASLG
FASLG
0.890
Biomarker
disease
MGD
Phenotypic, functional, and molecular genetic comparisons of the abnormal lymphoid cells of C3H-lpr/lpr and C3H-gld/gld mice.
3009614
1986
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Serological and histological characterization of the new mutant strain of lpr mice, CBA/KlJms-lprcg/lprcg.
2302830
1990
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
A new allele of the lpr locus, lprcg, that complements the gld gene in induction of lymphadenopathy in the mouse.
2406366
1990
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Transfer of Sjögren's syndrome-like autoimmune lesions into SCID mice and prevention of lesions by anti-CD4 and anti-T cell receptor antibody treatment.
7957574
1994
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Comparative influence of steroid hormones and immunosuppressive agents on autoimmune expression in lacrimal glands of a female mouse model of Sjögren's syndrome.
8163351
1994
×
Entrez Id:
356
Gene Symbol:
FASLG
FASLG
0.890
Biomarker
disease
MGD
gld/gld mice are unable to express a functional ligand for Fas.
7512035
1994
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Reduced cell-cell communication in a spontaneous murine model of autoimmune thyroid disease.
7628400
1995
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
GeneticVariation
disease
BEFREE
Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome .
7540117
1995
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
GeneticVariation
disease
UNIPROT
Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome .
7540117
1995
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Targeted mutation in the Fas gene causes hyperplasia in peripheral lymphoid organs and liver.
7581453
1995
TRBV20OR9-2
0.070
GeneticVariation
disease
BEFREE
Five unrelated children are described with a rare autoimmune lymphoproliferative syndrome (ALPS) characterized by massive nonmalignant lymphadenopathy, autoimmune phenomena, and expanded populations of TCR -CD3+CD4-CD8- lymphocytes.
7540117
1995
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
GeneticVariation
disease
UNIPROT
Fas gene mutations in the Canale-Smith syndrome , an inherited lymphoproliferative disorder associated with autoimmunity.
8929361
1996
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
GeneticVariation
disease
BEFREE
Fas gene mutations in the Canale-Smith syndrome , an inherited lymphoproliferative disorder associated with autoimmunity.
8929361
1996
×
Entrez Id:
355
Gene Symbol:
FAS
FAS
1.000
Biomarker
disease
MGD
Enhanced and accelerated lymphoproliferation in Fas-null mice.
8700897
1996