Found: 17
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Lack of Transmission of Chronic Wasting Disease Prions to Human Cerebral Organoids.
- Published in:
- Emerging Infectious Diseases, 2024, v. 30, n. 6, p. 1193, doi. 10.3201/eid3006.231568
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- Publication type:
- Article
Transmission characteristics of variably protease-sensitive prionopathy.
- Published in:
- 2014
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- Publication type:
- journal article
Preparation and Evaluation of Andrographolide Solid Dispersion Vectored by Silicon Dioxide.
- Published in:
- Pharmacognosy Magazine, 2016, v. 12, p. S245, doi. 10.4103/0973-1296.182156
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- Publication type:
- Article
Early onset and rapid course of Alzheimer disease associated with the I143T PSEN1 mutation.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P629, doi. 10.1016/j.jalz.2014.05.1095
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- Publication type:
- Article
Chronic Wasting Disease of Elk: Transmissibility to Humans Examined by Transgenic Mouse Models.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 35, p. 7944, doi. 10.1523/JNEUROSCI.2467-05.2005
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- Publication type:
- Article
Analysis and study on quality control methods and modes of traditional Chinese medicine preparations.
- Published in:
- China Journal of Chinese Materia Medica, 2012, v. 37, n. 9, p. 1332, doi. 10.4268/cjcmm20120934
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- Publication type:
- Article
United Plackett-Burman and Box-Behnken design to control formation of indirubin in process of preparing indigo naturalis.
- Published in:
- China Journal of Chinese Materia Medica, 2010, v. 35, n. 19, p. 2551, doi. 10.4268/cjcmm20101911
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- Publication type:
- Article
Study on mechanism of precursors transforming into indigo and indirubin in blue-genera plants.
- Published in:
- China Journal of Chinese Materia Medica, 2010, v. 35, n. 7, p. 928, doi. 10.4268/cjcmm20100728
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- Publication type:
- Article
Pathogenic Prion Protein Isoforms Are Not Present in Cerebral Organoids Generated from Asymptomatic Donors Carrying the E200K Mutation Associated with Familial Prion Disease.
- Published in:
- Pathogens, 2020, v. 9, n. 6, p. 482, doi. 10.3390/pathogens9060482
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- Publication type:
- Article
Correction: Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains.
- Published in:
- 2015
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- Publication type:
- Correction Notice
Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains.
- Published in:
- PLoS Pathogens, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.ppat.1004983
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- Publication type:
- Article
COASY variant as a new genetic cause of riboflavin-responsive lipid storage myopathy.
- Published in:
- Cell Discovery, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41421-023-00641-0
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- Publication type:
- Article
Sporadic and familial CJD: classification and characterisation.
- Published in:
- British Medical Bulletin, 2003, v. 66, n. 1, p. 213, doi. 10.1093/bmb/66.1.213
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- Publication type:
- Article
Stress and viral insults do not trigger E200K PrP conversion in human cerebral organoids.
- Published in:
- PLoS ONE, 2022, v. 17, n. 10, p. 1, doi. 10.1371/journal.pone.0277051
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- Publication type:
- Article
High-Yield α-Synuclein Purification and Ionic Strength Modification Pivotal to Seed Amplification Assay Performance and Reproducibility.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 11, p. 5988, doi. 10.3390/ijms25115988
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- Publication type:
- Article
Structural evidence for the critical role of the prion protein hydrophobic region in forming an infectious prion.
- Published in:
- PLoS Pathogens, 2019, v. 15, n. 12, p. 1, doi. 10.1371/journal.ppat.1008139
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- Publication type:
- Article
Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases.
- Published in:
- Molecular Brain, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13041-021-00864-w
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- Publication type:
- Article