Associated Papers
Dysregulation of inflammasomes in autoinflammatory diseases.
Hou C et al.
Joint Bone Spine, 2025
NLRP1- A CINDERELLA STORY: a perspective of recent advances in NLRP1 and the questions they raise.
Barry K et al.
Communications Biology, 2023
38104185 (PubMed )
Supplement: 42003_2023_5684_MOESM1_ESM.pdf
Current understanding of the phenotypic spectrum of patients with NLRP1 variants.
Takeichi T et al.
The British Journal of Dermatology, 2023
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings.
Li M et al.
The British Journal of Dermatology, 2023
NLRP1 Inflammasome Activation in Keratinocytes: Increasing Evidence of Important Roles in Inflammatory Skin Diseases and Immunity.
Fenini G et al.
The Journal of Investigative Dermatology, 2022
The NLRP1 Inflammasome Induces Pyroptosis in Human Corneal Epithelial Cells.
Griswold AR et al.
Investigative Ophthalmology & Visual Science, 2022
Pathogenic insights from genetic causes of autoinflammatory inflammasomopathies and interferonopathies.
Lin B et al.
The Journal of Allergy and Clinical Immunology, 2022
Molecular mechanisms of phenotypic variability in monogenic autoinflammatory diseases.
Aksentijevich I et al.
Nature Reviews. Rheumatology, 2021
The NLRP1 Inflammasome in Human Skin and Beyond.
Fenini G et al.
International Journal of Molecular Sciences, 2020
Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis.
Drutman SB et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019
NLRP1-associated autoinflammatory disease with epithelial dyskeratosis.
Lemus-Arteaga K et al.
Pediatric Dermatology, 0
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