The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome.
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Summary
The X chromosome-linked scurfy (sf) mutant of the mouse is recognized by the scaliness of the skin from which the name is derived and results in death of affected males at about 3-4 weeks of age.
- Type
- article
- Published
- 1990-04-01
- Cited by
- 199
- References
- 2
- Access
- Open access
- OpenAlex
- https://openalex.org/W2072227251
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:25455557
Keywords
Wiskott–Aldrich syndrome, Biology, Immunology, Mutant, Immunodeficiency
References
Cited by
- Mary Lyon: an appreciation.
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- X-linked immunodeficiencies.
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- Therapeutic Effects of Tumor Necrosis Factor Receptor Superfamily 25 (TNFRSF25)-Mediated Expansion of T-Regulatory Cells in Allergic Lung Inflammation and Airway Remodeling
- The Function of LAT in T Cell Activation and Autoimmunity
- Scurfy, the Foxp3 locus, and the molecular basis of peripheral tolerance.
- Immunology, Phenotype First: How Mutations Have Established New Principles and Pathways in Immunology - Preface
- Genetics of murine lung tumors.
- The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
- Cellular and molecular characterization of the scurfy mouse mutant.
- Type-1 immunity drives early lethality in scurfy mice
- X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
- The role of TCR specificity in the regulation of the immune response to self and commensal antigens
- The role of IL-27 and IL-35 in inflammatory diseases.
- Antiestrogens induce TGFß-mediated immunosuppression in breast cancer
- Interleukin‐21–Producing c‐Maf–Expressing CD4+ T Cells Induce Effector CD8+ T Cells and Enhance Autoimmune Inflammation in Scurfy Mice
- Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
- Immunodeficiencies with autoimmune consequences.
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