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Prions, prionoids and protein misfolding disorders.
Scheckel C, Aguzzi A. Scheckel C, et al. Nat Rev Genet. 2018 Jul;19(7):405-418. doi: 10.1038/s41576-018-0011-4. Nat Rev Genet. 2018. PMID: 29713012 Review.
We now know that prions consist of PrP(Sc), the pathological aggregated form of the cellular prion protein PrP(C). Over the years, the term has been semantically broadened to describe aggregates irrespective of their infectivity, and the prion concept is now being applied, …
We now know that prions consist of PrP(Sc), the pathological aggregated form of the cellular prion protein PrP(C). Over the years, th …
Genome-wide identification of microRNAs regulating the human prion protein.
Pease D, Scheckel C, Schaper E, Eckhardt V, Emmenegger M, Xenarios I, Aguzzi A. Pease D, et al. Among authors: scheckel c. Brain Pathol. 2019 Mar;29(2):232-244. doi: 10.1111/bpa.12679. Epub 2018 Dec 21. Brain Pathol. 2019. PMID: 30451334
The cellular prion protein (PrP(C) ) is best known for its misfolded disease-causing conformer, PrP(Sc) . Because the availability of PrP(C) is often limiting for prion propagation, understanding its regulation may point to possible therapeutic targets. We sought to …
The cellular prion protein (PrP(C) ) is best known for its misfolded disease-causing conformer, PrP(Sc) . Because the availability of …
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Zhou J, Park CY, Theesfeld CL, Wong AK, Yuan Y, Scheckel C, Fak JJ, Funk J, Yao K, Tajima Y, Packer A, Darnell RB, Troyanskaya OG. Zhou J, et al. Among authors: scheckel c. Nat Genet. 2019 Jun;51(6):973-980. doi: 10.1038/s41588-019-0420-0. Epub 2019 May 27. Nat Genet. 2019. PMID: 31133750 Free PMC article.
Genome-wide transcriptomics identifies an early preclinical signature of prion infection.
Sorce S, Nuvolone M, Russo G, Chincisan A, Heinzer D, Avar M, Pfammatter M, Schwarz P, Delic M, Müller M, Hornemann S, Sanoudou D, Scheckel C, Aguzzi A. Sorce S, et al. Among authors: scheckel c. PLoS Pathog. 2020 Jun 29;16(6):e1008653. doi: 10.1371/journal.ppat.1008653. eCollection 2020 Jun. PLoS Pathog. 2020. PMID: 32598380 Free PMC article.
Microexons--tiny but mighty.
Scheckel C, Darnell RB. Scheckel C, et al. EMBO J. 2015 Feb 3;34(3):273-4. doi: 10.15252/embj.201490651. Epub 2014 Dec 22. EMBO J. 2015. PMID: 25535247 Free PMC article.
Regulatory consequences of neuronal ELAV-like protein binding to coding and non-coding RNAs in human brain.
Scheckel C, Drapeau E, Frias MA, Park CY, Fak J, Zucker-Scharff I, Kou Y, Haroutunian V, Ma'ayan A, Buxbaum JD, Darnell RB. Scheckel C, et al. Elife. 2016 Feb 19;5:e10421. doi: 10.7554/eLife.10421. Elife. 2016. PMID: 26894958 Free PMC article.
Genome-wide analysis of GLD-1-mediated mRNA regulation suggests a role in mRNA storage.
Scheckel C, Gaidatzis D, Wright JE, Ciosk R. Scheckel C, et al. PLoS Genet. 2012 May;8(5):e1002742. doi: 10.1371/journal.pgen.1002742. Epub 2012 May 31. PLoS Genet. 2012. PMID: 22693456 Free PMC article.
LARP-1 promotes oogenesis by repressing fem-3 in the C. elegans germline.
Zanin E, Pacquelet A, Scheckel C, Ciosk R, Gotta M. Zanin E, et al. Among authors: scheckel c. J Cell Sci. 2010 Aug 15;123(Pt 16):2717-24. doi: 10.1242/jcs.066761. Epub 2010 Jul 27. J Cell Sci. 2010. PMID: 20663921
In C. elegans hermaphrodites, a complex regulatory network regulates the switch from sperm to oocyte production. We find that simultaneous depletion of larp-1 and the Nanos homologue nos-3 results in germline masculinization. ...
In C. elegans hermaphrodites, a complex regulatory network regulates the switch from sperm to oocyte production. We find that simulta …
Functional characterization of C. elegans Y-box-binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes.
Arnold A, Rahman MM, Lee MC, Muehlhaeusser S, Katic I, Gaidatzis D, Hess D, Scheckel C, Wright JE, Stetak A, Boag PR, Ciosk R. Arnold A, et al. Among authors: scheckel c. Nucleic Acids Res. 2014 Dec 1;42(21):13353-69. doi: 10.1093/nar/gku1077. Epub 2014 Nov 5. Nucleic Acids Res. 2014. PMID: 25378320 Free PMC article.
In this study, we set out to fill this gap and present a functional characterization of CEYs, the C. elegans Y-box-binding proteins. ...
In this study, we set out to fill this gap and present a functional characterization of CEYs, the C. elegans Y-box-binding proteins. …
A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not Aβ.
Kwart D, Gregg A, Scheckel C, Murphy EA, Paquet D, Duffield M, Fak J, Olsen O, Darnell RB, Tessier-Lavigne M. Kwart D, et al. Among authors: scheckel c. Neuron. 2019 Oct 23;104(2):256-270.e5. doi: 10.1016/j.neuron.2019.07.010. Epub 2019 Aug 12. Neuron. 2019. PMID: 31416668
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