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Feil Family Brain & Mind Research Institute

Publications

Found 4 results
Author Title Type [ Year(Asc)]
Filters: Author is Colak, Dilek  [Clear All Filters]
2019
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D et al..  2019.  Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.. Acta Neuropathol.
Dasouki MJ, Wakil SM, Al-Harazi O, Alkorashy M, Muiya NP, Andres E, Hagos S, Aldusery H, Dzimiri N, Colak D.  2019.  New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia.. OMICS.
Notaras M, Allen M, Longo F, Volk N, Toth M, Jeon NLi, Klann E, Colak D.  2019.  UPF2 leads to degradation of dendritically targeted mRNAs to regulate synaptic plasticity and cognitive function.. Mol Psychiatry.
2015
Deglincerti A, Liu Y, Colak D, Hengst U, Xu G, Jaffrey SR.  2015.  Coupled local translation and degradation regulate growth cone collapse.. Nat Commun. 6:6888.