These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
172 related articles for article (PubMed ID: 36194522)
1. Equally potent: Nlrp3 mutation in macrophages or neutrophils is sufficient to drive autoinflammation. Chen KW EMBO Rep; 2022 Nov; 23(11):e56091. PubMed ID: 36194522 [TBL] [Abstract][Full Text] [Related]
2. A Novel Mutation in the Pyrin Domain of the NOD-like Receptor Family Pyrin Domain Containing Protein 3 in Muckle-Wells Syndrome. Hu J; Zhu Y; Zhang JZ; Zhang RG; Li HM Chin Med J (Engl); 2017 Mar; 130(5):586-593. PubMed ID: 28229991 [TBL] [Abstract][Full Text] [Related]
3. Nlrp3 inflammasome activation in macrophages suffices for inducing autoinflammation in mice. Frising UC; Ribo S; Doglio MG; Malissen B; van Loo G; Wullaert A EMBO Rep; 2022 Jul; 23(7):e54339. PubMed ID: 35574994 [TBL] [Abstract][Full Text] [Related]
4. Computational Modeling of NLRP3 Identifies Enhanced ATP Binding and Multimerization in Cryopyrin-Associated Periodic Syndromes. Samson JM; Ravindran Menon D; Vaddi PK; Kalani Williams N; Domenico J; Zhai Z; Backos DS; Fujita M Front Immunol; 2020; 11():584364. PubMed ID: 33329557 [TBL] [Abstract][Full Text] [Related]
5. [Genetics of cryopyrin-associated periodic syndrome]. Kümmerle-Deschner JB; Lohse P Z Rheumatol; 2017 May; 76(4):313-321. PubMed ID: 28197772 [TBL] [Abstract][Full Text] [Related]
6. A case of cryopyrin-associated periodic syndrome due to somatic mosaic mutation complicated with recurrent circinate erythematous psoriasis. Ando T; Abe Y; Yamaji K; Nishikomori R; Tamura N Mod Rheumatol Case Rep; 2024 Jul; 8(2):368-372. PubMed ID: 38036300 [TBL] [Abstract][Full Text] [Related]
11. NLRP3 A439V Mutation in a Large Family with Cryopyrin-associated Periodic Syndrome: Description of Ophthalmologic Symptoms in Correlation with Other Organ Symptoms. Sobolewska B; Angermair E; Deuter C; Doycheva D; Kuemmerle-Deschner J; Zierhut M J Rheumatol; 2016 Jun; 43(6):1101-6. PubMed ID: 27134254 [TBL] [Abstract][Full Text] [Related]
12. Identification of a variant in NLRP3 gene in a patient with Muckle-Wells syndrome: a case report and review of literature. Liu J; Zhang R; Yi Z; Lin Y; Chang H; Zhang Q Pediatr Rheumatol Online J; 2023 Feb; 21(1):15. PubMed ID: 36765385 [TBL] [Abstract][Full Text] [Related]