Found: 15
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Personalized Treatment for Infantile Ascending Hereditary Spastic Paralysis Based on In Silico Strategies.
- Published in:
- Molecules, 2022, v. 27, n. 20, p. 7063, doi. 10.3390/molecules27207063
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- Article
Monitoring the autophagy-endolysosomal system using monomeric Keima-fused MAP1LC3B.
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- PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0234180
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- Article
Defective relocalization of ALS2/alsin missense mutants to Rac1-induced macropinosomes accounts for loss of their cellular function and leads to disturbed amphisome formation
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- FEBS Letters, 2011, v. 585, n. 5, p. 730, doi. 10.1016/j.febslet.2011.01.045
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- Article
Functional links between SQSTM1 and ALS2 in the pathogenesis of ALS: cumulative impact on the protection against mutant SOD1-mediated motor dysfunction in mice.
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- Human Molecular Genetics, 2016, v. 25, n. 15, p. 3321, doi. 10.1093/hmg/ddw180
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- Article
GRP78 Suppresses Lipid Peroxidation and Promotes Cellular Antioxidant Levels in Glial Cells following Hydrogen Peroxide Exposure.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0086951
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- Article
Different Human Copper-Zinc Superoxide Dismutase Mutants, SOD1<sup>G93A</sup> and SOD1<sup>H46R</sup>, Exert Distinct Harmful Effects on Gross Phenotype in Mice.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033409
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- Article
Loss of ALS2/Alsin Exacerbates Motor Dysfunction in a SOD1<sup>H46R</sup>-Expressing Mouse ALS Model by Disturbing Endolysosomal Trafficking.
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- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009805
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- Article
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
- Published in:
- Nature Genetics, 2001, v. 29, n. 2, p. 166, doi. 10.1038/ng1001-166
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- Article
Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking.
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- Human Molecular Genetics, 2006, v. 15, n. 2, p. 233, doi. 10.1093/hmg/ddi440
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- Article
ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamics.
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- Human Molecular Genetics, 2003, v. 12, n. 14, p. 1671, doi. 10.1093/hmg/ddg184
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- Article
Systemic overexpression of SQSTM1/p62 accelerates disease onset in a SOD1<sup>H46R</sup>-expressing ALS mouse model.
- Published in:
- Molecular Brain, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13041-018-0373-8
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- Article
Efficient differentiation and polarization of primary cultured neurons on poly(lactic acid) scaffolds with microgrooved structures.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63537-z
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- Article
Human PZP and common marmoset A2ML1 as pregnancy related proteins.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61714-8
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- Article
Dysregulation of the Autophagy-Endolysosomal System in Amyotrophic Lateral Sclerosis and Related Motor Neuron Diseases.
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- Neurology Research International, 2012, p. 1, doi. 10.1155/2012/498428
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- Article
ALS2CL, the novel protein highly homologous to the carboxy-terminal half of ALS2, binds to Rab5 and modulates endosome dynamics
- Published in:
- FEBS Letters, 2004, v. 575, n. 1-3, p. 64, doi. 10.1016/j.febslet.2004.07.092
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- Article