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Results by year

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

Year Number of Results
2002 1
2003 1
2004 1
2005 2
2006 1
2007 1
2008 3
2009 2
2010 4
2011 2
2012 1
2013 2
2014 2
2015 4
2016 1
2017 3
2018 4
2019 2
2021 2
2022 5
2023 2
2024 0

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PubMed for id: 200162

34 results

Results by year

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Page 1
Reduced SPAG17 Expression in Systemic Sclerosis Triggers Myofibroblast Transition and Drives Fibrosis.
Sapao P, Roberson EDO, Shi B, Assassi S, Skaug B, Lee F, Naba A, Perez White BE, Córdova-Fletes C, Tsou PS, Sawalha AH, Gudjonsson JE, Ma F, Verma P, Bhattacharyya D, Carns M, Strauss JF 3rd, Sicard D, Tschumperlin DJ, Champer MI, Campagnola PJ, Teves ME, Varga J. Sapao P, et al. J Invest Dermatol. 2023 Feb;143(2):284-293. doi: 10.1016/j.jid.2022.08.052. Epub 2022 Sep 15. J Invest Dermatol. 2023. PMID: 36116512 Free PMC article.
Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies.
Córdova-Fletes C, Becerra-Solano LE, Rangel-Sosa MM, Rivas-Estilla AM, Alberto Galán-Huerta K, Ortiz-López R, Rojas-Martínez A, Juárez-Vázquez CI, García-Ortiz JE. Córdova-Fletes C, et al. Eur J Med Genet. 2018 Mar;61(3):161-167. doi: 10.1016/j.ejmg.2017.11.011. Epub 2017 Nov 23. Eur J Med Genet. 2018. PMID: 29174089
Spag17 deficiency results in skeletal malformations and bone abnormalities.
Teves ME, Sundaresan G, Cohen DJ, Hyzy SL, Kajan I, Maczis M, Zhang Z, Costanzo RM, Zweit J, Schwartz Z, Boyan BD, Strauss JF 3rd. Teves ME, et al. PLoS One. 2015 May 27;10(5):e0125936. doi: 10.1371/journal.pone.0125936. eCollection 2015. PLoS One. 2015. PMID: 26017218 Free PMC article.
34 results