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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 1 |
2017 | 3 |
2018 | 2 |
2019 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 83479
5 results
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MicroRNA-628-5p inhibits cell proliferation in glioma by targeting DDX59.
J Cell Biochem. 2019 Oct;120(10):17293-17302. doi: 10.1002/jcb.28991. Epub 2019 May 20.
J Cell Biochem. 2019.
PMID: 31111544
EGFR and Ras regulate DDX59 during lung cancer development.
Yang L, Zhang H, Chen D, Ding P, Yuan Y, Zhang Y.
Yang L, et al.
Gene. 2018 Feb 5;642:95-102. doi: 10.1016/j.gene.2017.11.029. Epub 2017 Nov 10.
Gene. 2018.
PMID: 29133145
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A loss-of-function homozygous mutation in DDX59 implicates a conserved DEAD-box RNA helicase in nervous system development and function.
Salpietro V, Efthymiou S, Manole A, Maurya B, Wiethoff S, Ashokkumar B, Cutrupi MC, Dipasquale V, Manti S, Botia JA, Ryten M, Vandrovcova J, Bello OD, Bettencourt C, Mankad K, Mukherjee A, Mutsuddi M, Houlden H.
Salpietro V, et al.
Hum Mutat. 2018 Feb;39(2):187-192. doi: 10.1002/humu.23368. Epub 2017 Nov 27.
Hum Mutat. 2018.
PMID: 29127725
Free PMC article.
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Confirmation that mutations in DDX59 cause an autosomal recessive form of oral-facial-digital syndrome: Further delineation of the DDX59 phenotype in two new families.
Faily S, Perveen R, Urquhart J, Chandler K, Clayton-Smith J.
Faily S, et al.
Eur J Med Genet. 2017 Oct;60(10):527-532. doi: 10.1016/j.ejmg.2017.07.009. Epub 2017 Jul 12.
Eur J Med Genet. 2017.
PMID: 28711741
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Mutations in DDX59 implicate RNA helicase in the pathogenesis of orofaciodigital syndrome.
Shamseldin HE, Rajab A, Alhashem A, Shaheen R, Al-Shidi T, Alamro R, Al Harassi S, Alkuraya FS.
Shamseldin HE, et al.
Am J Hum Genet. 2013 Sep 5;93(3):555-60. doi: 10.1016/j.ajhg.2013.07.012. Epub 2013 Aug 22.
Am J Hum Genet. 2013.
PMID: 23972372
Free PMC article.
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