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Corrigendum: Parkinson-causing α-synuclein missense mutations shift native tetramers to monomers as a mechanism for disease initiation.
- Published in:
- Nature Communications, 2015, v. 6, n. 7, p. 8008, doi. 10.1038/ncomms9008
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- Publication type:
- Article
Parkinson-causing α-synuclein missense mutations shift native tetramers to monomers as a mechanism for disease initiation.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7314, doi. 10.1038/ncomms8314
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- Publication type:
- Article
Loss of native α-synuclein multimerization by strategically mutating its amphipathic helix causes abnormal vesicle interactions in neuronal cells.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 18, p. 3466, doi. 10.1093/hmg/ddx227
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- Publication type:
- Article
A good gut feeling on Sarm1-mediated axon degeneration.
- Published in:
- Protein & Cell, 2021, v. 12, n. 8, p. 596, doi. 10.1007/s13238-021-00842-x
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- Publication type:
- Article
The <italic>T</italic>rem<italic>2</italic> R47H variant confers loss-of-function-like phenotypes in Alzheimer's disease.
- Published in:
- Molecular Neurodegeneration, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13024-018-0262-8
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- Publication type:
- Article
TREM2 in Neurodegenerative Diseases.
- Published in:
- Molecular Neurodegeneration, 2017, v. 12, p. 1, doi. 10.1186/s13024-017-0197-5
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- Publication type:
- Article