Found: 14
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Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation.
- Published in:
- EMBO Molecular Medicine, 2015, v. 7, n. 3, p. 339, doi. 10.15252/emmm.201404588
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- Article
Disruption of the c‐terminal serine protease domain of Fam111a does not alter calcium homeostasis in mice.
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- Physiological Reports, 2024, v. 12, n. 9, p. 1, doi. 10.14814/phy2.15977
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- Article
Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope.
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- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01132-y
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- Article
Still Heart Encodes a Structural HMT, SMYD1b, with Chaperone-Like Function during Fast Muscle Sarcomere Assembly.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0142528
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- Article
Amyloid Beta Precursor Protein and Prion Protein Have a Conserved Interaction Affecting Cell Adhesion and CNS Development.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051305
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- Article
Frequent Missense and Insertion/Deletion Polymorphisms in the Ovine Shadoo Gene Parallel Species-Specific Variation in PrP.
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- PLoS ONE, 2009, v. 4, n. 8, p. 1, doi. 10.1371/journal.pone.0006538
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- Article
Endoproteolytic processing of the mammalian prion glycoprotein family.
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- FEBS Journal, 2014, v. 281, n. 3, p. 862, doi. 10.1111/febs.12654
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- Article
Wild-type Shadoo proteins convert to amyloid-like forms under native conditions.
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- Journal of Neurochemistry, 2010, v. 113, n. 1, p. 92, doi. 10.1111/j.1471-4159.2010.06575.x
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- Article
Susceptibility of Beavers to Chronic Wasting Disease.
- Published in:
- Biology (2079-7737), 2022, v. 11, n. 5, p. 667, doi. 10.3390/biology11050667
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- Article
Correction: Still Heart Encodes a Structural HMT, SMYD1b, with Chaperone-Like Function during Fast Muscle Sarcomere Assembly.
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- 2016
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- Correction Notice
A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.
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- PLoS Pathogens, 2018, v. 14, n. 1, p. 1, doi. 10.1371/journal.ppat.1006826
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- Article
Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation.
- Published in:
- 2021
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- Correction Notice
Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1045, doi. 10.1007/s00401-020-02148-4
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- Publication type:
- Article
Investigating CRISPR/Cas9 gene drive for production of disease-preventing prion gene alleles.
- Published in:
- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269342
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- Article