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Cited by 472

The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.

Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease.

Open access
Wu, J, Wilson, J, He, J, Xiang, L, Schur, P H, Mountz, J D·1996·Journal of Clinical Investigation

Abstract

The pathogenesis of systemic lupus erythematosus (SLE) is multifactorial and multigenetic. The apoptosis genes, fas and fas ligand (fasL), are candidate contributory genes in human SLE, as mutations of these genes result in autoimmunity in several murine models of this disease. In humans, fas mutations result in a familial autoimmune lymphoproliferative syndrome, but defects in FasL have not yet been identified. In this study, DNA from 75 patients with SLE was screened by single-stranded conformational polymorphism analysis for potential mutations of the extracellular domain of FasL. A heterozygous single-stranded conformational polymorphism for FasL, was identified in one SLE patient, who exhibited lymphadenopathy. Molecular cloning and sequencing indicated that the genomic DNA of this patient contained an 84-bp deletion within exon 4 of the fasL gene, resulting in a predicted 28 amino acid in-frame deletion. Analysis of PBMC from this patient revealed decreased FasL activity, decreased activation-induced cell death, and increased T cell proliferation after activation. This is the first report of defective FasL-mediated apoptosis related to a mutation of the human Fasl, gene in a patient with SLE and suggests that fasL mutations are an uncommon cause of the disease.

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Metadata

Authors
Wu, J., Wilson, J., He, J., Xiang, L., Schur, P. H., & Mountz, J. D.
Venue
Journal of Clinical Investigation
Published
1996-09-01
Volume
98
Issue
5
Pages
1107-1113
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2074280352
Cited by
472
References
31
FWCI
19.19
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease. https://app.cochat.ai/papers/10.1172/jci118892
The paper
Wu, J., Wilson, J., He, J., Xiang, L., Schur, P. H., & Mountz, J. D. (1996). Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease. Journal of Clinical Investigation. https://doi.org/10.1172/jci118892

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.