Deriziotis P - Search Results

1

Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry.

Deriziotis P, André R, Smith DM, Goold R, Kinghorn KJ, Kristiansen M, Nathan JA, Rosenzweig R, Krutauz D, Glickman MH, Collinge J, Goldberg AL, Tabrizi SJ. Deriziotis P, et al. EMBO J. 2011 Jul 8;30(15):3065-77. doi: 10.1038/emboj.2011.224. EMBO J. 2011. PMID: 21743439 Free PMC article.

2

Disease-associated prion protein oligomers inhibit the 26S proteasome.

Kristiansen M, Deriziotis P, Dimcheff DE, Jackson GS, Ovaa H, Naumann H, Clarke AR, van Leeuwen FW, Menéndez-Benito V, Dantuma NP, Portis JL, Collinge J, Tabrizi SJ. Kristiansen M, et al. Among authors: deriziotis p. Mol Cell. 2007 Apr 27;26(2):175-88. doi: 10.1016/j.molcel.2007.04.001. Mol Cell. 2007. PMID: 17466621 Free article.

3

Prions and the proteasome.

Deriziotis P, Tabrizi SJ. Deriziotis P, et al. Biochim Biophys Acta. 2008 Dec;1782(12):713-22. doi: 10.1016/j.bbadis.2008.06.011. Epub 2008 Jul 1. Biochim Biophys Acta. 2008. PMID: 18644436 Free article. Review.

4

Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.

Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J. Mead S, et al. Among authors: deriziotis p. Lancet Neurol. 2009 Jan;8(1):57-66. doi: 10.1016/S1474-4422(08)70265-5. Lancet Neurol. 2009. PMID: 19081515 Free PMC article.

5

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.

Dias C, Estruch SB, Graham SA, McRae J, Sawiak SJ, Hurst JA, Joss SK, Holder SE, Morton JE, Turner C, Thevenon J, Mellul K, Sánchez-Andrade G, Ibarra-Soria X, Deriziotis P, Santos RF, Lee SC, Faivre L, Kleefstra T, Liu P, Hurles ME; DDD Study; Fisher SE, Logan DW. Dias C, et al. Among authors: deriziotis p. Am J Hum Genet. 2016 Aug 4;99(2):253-74. doi: 10.1016/j.ajhg.2016.05.030. Epub 2016 Jul 21. Am J Hum Genet. 2016. PMID: 27453576 Free PMC article.

6

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.

Lozano R, Vino A, Lozano C, Fisher SE, Deriziotis P. Lozano R, et al. Among authors: deriziotis p. Eur J Hum Genet. 2015 Dec;23(12):1702-7. doi: 10.1038/ejhg.2015.66. Epub 2015 Apr 8. Eur J Hum Genet. 2015. PMID: 25853299 Free PMC article.

7

Insights into the genetic foundations of human communication.

Graham SA, Deriziotis P, Fisher SE. Graham SA, et al. Among authors: deriziotis p. Neuropsychol Rev. 2015 Mar;25(1):3-26. doi: 10.1007/s11065-014-9277-2. Epub 2015 Jan 18. Neuropsychol Rev. 2015. PMID: 25597031 Review.

8

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE. Sollis E, et al. Among authors: deriziotis p. Hum Mol Genet. 2016 Feb 1;25(3):546-57. doi: 10.1093/hmg/ddv495. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647308

9

Estruch SB, Graham SA, Deriziotis P, Fisher SE. Estruch SB, et al. Among authors: deriziotis p. Sci Rep. 2016 Feb 12;6:20911. doi: 10.1038/srep20911. Sci Rep. 2016. PMID: 26867680 Free PMC article.

10

Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.

Deriziotis P, Graham SA, Estruch SB, Fisher SE. Deriziotis P, et al. J Vis Exp. 2014 May 26;(87):51438. doi: 10.3791/51438. J Vis Exp. 2014. PMID: 24893771 Free PMC article.

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