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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1995 3
1996 6
1997 3
1998 3
1999 5
2001 3
2002 11
2003 7
2004 9
2005 5
2006 4
2007 7
2008 10
2009 13
2010 15
2011 11
2012 8
2013 9
2014 9
2015 16
2016 11
2017 14
2018 4
2019 8
2020 14
2021 17
2022 12
2023 9
2024 0

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PubMed (RefSeq) for id: 2217290831

227 results

Results by year

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Page 1
Investigation of the impact of AXL, TLR3, and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein-protein interaction network analyses.
Gomes JA, Sgarioni E, Boquett JA, Kowalski TW, Fraga LR, Terças-Trettel ACP, da Silva JH, Ribeiro BFR, Galera MF, de Oliveira TM, Carvalho de Andrade MDF, Carvalho IF, Schüler-Faccini L, Vianna FSL. Gomes JA, et al. Birth Defects Res. 2023 Oct 1;115(16):1500-1512. doi: 10.1002/bdr2.2232. Epub 2023 Aug 1. Birth Defects Res. 2023. PMID: 37526179
Human inherited complete STAT2 deficiency underlies inflammatory viral diseases.
Bucciol G, Moens L, Ogishi M, Rinchai D, Matuozzo D, Momenilandi M, Kerrouche N, Cale CM, Treffeisen ER, Al Salamah M, Al-Saud BK, Lachaux A, Duclaux-Loras R, Meignien M, Bousfiha A, Benhsaien I, Shcherbina A, Roppelt A; COVID Human Genetic Effort; Gothe F, Houhou-Fidouh N, Hackett SJ, Bartnikas LM, Maciag MC, Alosaimi MF, Chou J, Mohammed RW, Freij BJ, Jouanguy E, Zhang SY, Boisson-Dupuis S, Béziat V, Zhang Q, Duncan CJ, Hambleton S, Casanova JL, Meyts I. Bucciol G, et al. J Clin Invest. 2023 Jun 15;133(12):e168321. doi: 10.1172/JCI168321. J Clin Invest. 2023. PMID: 36976641 Free PMC article.
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2.
Zhu G, Badonyi M, Franklin L, Seabra L, Rice GI, Anne-Boland-Auge, Deleuze JF, El-Chehadeh S, Anheim M, de Saint-Martin A, Pellegrini S, Marsh JA, Crow YJ, El-Daher MT. Zhu G, et al. J Clin Immunol. 2023 May;43(4):808-818. doi: 10.1007/s10875-023-01445-3. Epub 2023 Feb 8. J Clin Immunol. 2023. PMID: 36753016 Free PMC article.
227 results