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Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
Brehm A, Liu Y, Sheikh A, Marrero B, Omoyinmi E, Zhou Q, Montealegre G, Biancotto A, Reinhardt A, Almeida de Jesus A, Pelletier M, Tsai WL, Remmers EF, Kardava L, Hill S, Kim H, Lachmann HJ, Megarbane A, Chae JJ, Brady J, Castillo RD, Brown D, Casano AV, Gao L, Chapelle D, Huang Y, Stone D, Chen Y, Sotzny F, Lee CC, Kastner DL, Torrelo A, Zlotogorski A, Moir S, Gadina M, McCoy P, Wesley R, Rother KI, Hildebrand PW, Brogan P, Krüger E, Aksentijevich I, Goldbach-Mansky R. Brehm A, et al. Among authors: omoyinmi e. J Clin Invest. 2015 Nov 2;125(11):4196-211. doi: 10.1172/JCI81260. Epub 2015 Oct 20. J Clin Invest. 2015. PMID: 26524591 Free PMC article.
Gene hunting in autoinflammation.
Standing A, Omoyinmi E, Brogan P. Standing A, et al. Among authors: omoyinmi e. Clin Transl Allergy. 2013 Sep 26;3(1):32. doi: 10.1186/2045-7022-3-32. Clin Transl Allergy. 2013. PMID: 24070009 Free PMC article.
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
Brehm A, Liu Y, Sheikh A, Marrero B, Omoyinmi E, Zhou Q, Montealegre G, Biancotto A, Reinhardt A, de Jesus AA, Pelletier M, Tsai WL, Remmers EF, Kardava L, Hill S, Kim H, Lachmann HJ, Megarbane A, Chae JJ, Brady J, Castillo RD, Brown D, Casano AV, Gao L, Chapelle D, Huang Y, Stone D, Chen Y, Sotzny F, Lee CC, Kastner DL, Torrelo A, Zlotogorski A, Moir S, Gadina M, McCoy P, Wesley R, Rother KI, Hildebrand PW, Brogan P, Krüger E, Aksentijevich I, Goldbach-Mansky R. Brehm A, et al. Among authors: omoyinmi e. J Clin Invest. 2016 Feb;126(2):795. doi: 10.1172/JCI86020. Epub 2016 Feb 1. J Clin Invest. 2016. PMID: 26829627 Free PMC article. No abstract available.
Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.
Rowczenio DM, Trojer H, Omoyinmi E, Aróstegui JI, Arakelov G, Mensa-Vilaro A, Baginska A, Silva Pilorz C, Wang G, Lane T, Brogan P, Hawkins PN, Lachmann HJ. Rowczenio DM, et al. Among authors: omoyinmi e. Arthritis Rheumatol. 2016 Aug;68(8):2044-9. doi: 10.1002/art.39683. Arthritis Rheumatol. 2016. PMID: 26992170
TRAP1 chaperone protein mutations and autoinflammation.
Standing AS, Hong Y, Paisan-Ruiz C, Omoyinmi E, Medlar A, Stanescu H, Kleta R, Rowcenzio D, Hawkins P, Lachmann H, McDermott MF, Eleftheriou D, Klein N, Brogan PA. Standing AS, et al. Among authors: omoyinmi e. Life Sci Alliance. 2019 Dec 27;3(2):e201900376. doi: 10.26508/lsa.201900376. Print 2020 Feb. Life Sci Alliance. 2019. PMID: 31882397 Free PMC article.
De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis.
Mauro A, Omoyinmi E, Sebire NJ, Barnicoat A, Brogan P. Mauro A, et al. Among authors: omoyinmi e. Case Rep Pediatr. 2017;2017:9682803. doi: 10.1155/2017/9682803. Epub 2017 Apr 24. Case Rep Pediatr. 2017. PMID: 28523199 Free PMC article.
46 results