Gruber et al., 2020 - Google Patents
Homozygous STAT2 gain-of-function mutation by loss of USP18 activity in a patient with type I interferonopathyGruber et al., 2020
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- 9879206252977885974
- Author
- Gruber C
- Martin-Fernandez M
- Ailal F
- Qiu X
- Taft J
- Altman J
- Rosain J
- Buta S
- Bousfiha A
- Casanova J
- Bustamante J
- Bogunovic D
- Publication year
- Publication venue
- Journal of Experimental Medicine
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Snippet
Type I interferonopathies are monogenic disorders characterized by enhanced type I interferon (IFN-I) cytokine activity. Inherited USP18 and ISG15 deficiencies underlie type I interferonopathies by preventing the regulation of late responses to IFN-I. Specifically …
- 102000004265 STAT2 Transcription Factor 0 title abstract description 147
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
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- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
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- G01N33/53—Immunoassay; Biospecific binding assay
- G01N33/564—Immunoassay; Biospecific binding assay for pre-existing immune complex or autoimmune disease, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9
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