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

Year Number of Results
2002 2
2003 2
2004 1
2005 3
2006 3
2007 6
2008 13
2009 16
2010 15
2011 27
2012 25
2013 42
2014 41
2015 57
2016 53
2017 59
2018 70
2019 70
2020 46
2021 56
2022 26
2023 33
2024 6

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PubMed (GeneRIF) for id: 6935

581 results

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Page 1
ZEB1 shapes AML immunological niches, suppressing CD8 T cell activity while fostering Th17 cell expansion.
Bassani B, Simonetti G, Cancila V, Fiorino A, Ciciarello M, Piva A, Khorasani AM, Chiodoni C, Lecis D, Gulino A, Fonzi E, Botti L, Portararo P, Costanza M, Brambilla M, Colombo G, Schwaller J, Tzankov A, Ponzoni M, Ciceri F, Bolli N, Curti A, Tripodo C, Colombo MP, Sangaletti S. Bassani B, et al. Cell Rep. 2024 Feb 27;43(2):113794. doi: 10.1016/j.celrep.2024.113794. Epub 2024 Feb 15. Cell Rep. 2024. PMID: 38363677 Free article.
ZEB1 hypermethylation is associated with better prognosis in patients with colon cancer.
Fernandez-De-Los-Reyes I, Gomez-Dorronsoro M, Monreal-Santesteban I, Fernandez-Fernandez A, Fraga M, Azcue P, Alonso L, Fernandez-Marlasca B, Suarez J, Cordoba-Iturriagagoitia A, Guerrero-Setas D. Fernandez-De-Los-Reyes I, et al. Clin Epigenetics. 2023 Dec 13;15(1):193. doi: 10.1186/s13148-023-01605-7. Clin Epigenetics. 2023. PMID: 38093305 Free PMC article.
The EMT factor ZEB1 paradoxically inhibits EMT in BRAF-mutant carcinomas.
Sánchez-Tilló E, Pedrosa L, Vila I, Chen Y, Győrffy B, Sánchez-Moral L, Siles L, Lozano JJ, Esteve-Codina A, Darling DS, Cuatrecasas M, Castells A, Maurel J, Postigo A. Sánchez-Tilló E, et al. JCI Insight. 2023 Oct 23;8(20):e164629. doi: 10.1172/jci.insight.164629. JCI Insight. 2023. PMID: 37870961 Free PMC article.
Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.
Heide S, Argilli E, Valence S, Boutaud L, Roux N, Mignot C, Nava C, Keren B, Giraudat K, Faudet A, Gerasimenko A, Garel C, Blondiaux E, Rastetter A, Grevent D, Le C, Mackenzie L, Richards L, Attié-Bitach T, Depienne C, Sherr E, Héron D. Heide S, et al. J Med Genet. 2024 Feb 21;61(3):244-249. doi: 10.1136/jmg-2023-109293. J Med Genet. 2024. PMID: 37857482
581 results