Scheckel C - Search Results

1

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.

2

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.

3

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.

4

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 Free article.

5

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 Dec 4;104(5):1022. doi: 10.1016/j.neuron.2019.11.010. Neuron. 2019. PMID: 31805257 Free article. No abstract available.

6

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.

7

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 Free PMC article.

8

Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons.

Scheckel C, Imeri M, Schwarz P, Aguzzi A. Scheckel C, et al. Elife. 2020 Sep 22;9:e62911. doi: 10.7554/eLife.62911. Elife. 2020. PMID: 32960170 Free PMC article.

9

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.

10

Soluble dimeric prion protein ligand activates Adgrg6 receptor but does not rescue early signs of demyelination in PrP-deficient mice.

Henzi A, Senatore A, Lakkaraju AKK, Scheckel C, Mühle J, Reimann R, Sorce S, Schertler G, Toyka KV, Aguzzi A. Henzi A, et al. Among authors: scheckel c. PLoS One. 2020 Nov 12;15(11):e0242137. doi: 10.1371/journal.pone.0242137. eCollection 2020. PLoS One. 2020. PMID: 33180885 Free PMC article.

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