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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2013 | 1 |
2014 | 1 |
2018 | 1 |
2020 | 2 |
2021 | 3 |
2024 | 0 |
PubMed (GeneRIF) for id: 161725
7 results
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Page 1
SPOP and OTUD7A Control EWS-FLI1 Protein Stability to Govern Ewing Sarcoma Growth.
Adv Sci (Weinh). 2021 Jul;8(14):e2004846. doi: 10.1002/advs.202004846. Epub 2021 Jun 1.
Adv Sci (Weinh). 2021.
PMID: 34060252
Free PMC article.
CircRNA_OTUD7A upregulates FOXP1 expression to facilitate the progression of diffuse large B-cell lymphoma via acting as a sponge of miR-431-5p.
Liu W, Lei L, Liu X, Ye S.
Liu W, et al.
Genes Genomics. 2021 Jun;43(6):653-667. doi: 10.1007/s13258-021-01094-z. Epub 2021 Apr 8.
Genes Genomics. 2021.
PMID: 33830472
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Biallelic loss of OTUD7A causes severe muscular hypotonia, intellectual disability, and seizures.
Suzuki H, Inaba M, Yamada M, Uehara T, Takenouchi T, Mizuno S, Kosaki K, Doi M.
Suzuki H, et al.
Am J Med Genet A. 2021 Apr;185(4):1182-1186. doi: 10.1002/ajmg.a.62054. Epub 2020 Dec 31.
Am J Med Genet A. 2021.
PMID: 33381903
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Report of the first patient with a homozygous OTUD7A variant responsible for epileptic encephalopathy and related proteasome dysfunction.
Garret P, Ebstein F, Delplancq G, Dozieres-Puyravel B, Boughalem A, Auvin S, Duffourd Y, Klafack S, Zieba BA, Mahmoudi S, Singh KK, Duplomb L, Thauvin-Robinet C, Costa JM, Krüger E, Trost D, Verloes A, Faivre L, Vitobello A.
Garret P, et al.
Clin Genet. 2020 Apr;97(4):567-575. doi: 10.1111/cge.13709. Epub 2020 Feb 11.
Clin Genet. 2020.
PMID: 31997314
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OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome.
Uddin M, Unda BK, Kwan V, Holzapfel NT, White SH, Chalil L, Woodbury-Smith M, Ho KS, Harward E, Murtaza N, Dave B, Pellecchia G, D'Abate L, Nalpathamkalam T, Lamoureux S, Wei J, Speevak M, Stavropoulos J, Hope KJ, Doble BW, Nielsen J, Wassman ER, Scherer SW, Singh KK.
Uddin M, et al.
Am J Hum Genet. 2018 Feb 1;102(2):278-295. doi: 10.1016/j.ajhg.2018.01.006.
Am J Hum Genet. 2018.
PMID: 29395074
Free PMC article.
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Snail1-dependent transcriptional repression of Cezanne2 in hepatocellular carcinoma.
Xu Z, Pei L, Wang L, Zhang F, Hu X, Gui Y.
Xu Z, et al.
Oncogene. 2014 May 29;33(22):2836-45. doi: 10.1038/onc.2013.243. Epub 2013 Jun 24.
Oncogene. 2014.
PMID: 23792447
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Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.
Morrison AC, Felix JF, Cupples LA, Glazer NL, Loehr LR, Dehghan A, Demissie S, Bis JC, Rosamond WD, Aulchenko YS, Wang YA, Haritunians T, Folsom AR, Rivadeneira F, Benjamin EJ, Lumley T, Couper D, Stricker BH, O'Donnell CJ, Rice KM, Chang PP, Hofman A, Levy D, Rotter JI, Fox ER, Uitterlinden AG, Wang TJ, Psaty BM, Willerson JT, van Duijn CM, Boerwinkle E, Witteman JC, Vasan RS, Smith NL.
Morrison AC, et al.
Circ Cardiovasc Genet. 2010 Jun;3(3):248-55. doi: 10.1161/CIRCGENETICS.109.895995. Epub 2010 Apr 17.
Circ Cardiovasc Genet. 2010.
PMID: 20400778
Free PMC article.
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