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PARKINSON’S DISEASE-ASSOCIATED MUTATIONS IN LRRK2 CAUSE CENTROSOMAL DEFECTS VIA RAB8A PHOSPHORYLATION.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1501, doi. 10.1016/j.jalz.2017.07.604
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- Article
P3-374: PINK1 transfected cell lines exhibit mitochondrial protection in vitro when exposed to mitochondrial toxins
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- 2006
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- Abstract
P3-374: PINK1 transfected cell lines exhibit mitochondrial protection in vitro when exposed to mitochondrial toxins
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- 2006
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- Abstract
Biochemical Characterization of Highly Purified Leucine-Rich Repeat Kinases 1 and 2 Demonstrates Formation of Homodimers.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043472
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- Article
LRRK2 Kinase Activity Is Dependent on LRRK2 GTP Binding Capacity but Independent of LRRK2 GTP Binding.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023207
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- Article
The Parkinson's Disease Associated LRRK2 Exhibits Weaker In Vitro Phosphorylation of 4E-BP Compared to Autophosphorylation.
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- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008730
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- Article
Mitochondrial Alterations in PINK1 Deficient Cells Are Influenced by Calcineurin-Dependent Dephosphorylation of Dynamin-Related Protein 1.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005701
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- Article
Correction to: Molecular mechanism of olesoxime-mediated neuroprotection through targeting α-synuclein interaction with mitochondrial VDAC.
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- 2020
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- Correction Notice
Molecular mechanism of olesoxime-mediated neuroprotection through targeting α-synuclein interaction with mitochondrial VDAC.
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- Cellular & Molecular Life Sciences, 2020, v. 77, n. 18, p. 3611, doi. 10.1007/s00018-019-03386-w
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- Article
Correction: Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia.
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- 2022
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- Correction Notice
Mutations in LRRK2 linked to Parkinson disease sequester Rab8a to damaged lysosomes and regulate transferrin-mediated iron uptake in microglia.
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- PLoS Biology, 2021, v. 19, n. 12, p. 1, doi. 10.1371/journal.pbio.3001480
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- Article
Comparative Protein Interaction Network Analysis Identifies Shared and Distinct Functions for the Human ROCO Proteins.
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- Proteomics, 2018, v. 18, n. 10, p. 1, doi. 10.1002/pmic.201700444
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- Article
Phosphorylation of LRRK2 by casein kinase 1α regulates trans-Golgi clustering via differential interaction with ARHGEF7.
- Published in:
- Nature Communications, 2014, v. 5, n. 12, p. 5827, doi. 10.1038/ncomms6827
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- Article
Genes associated with Parkinson's disease: regulation of autophagy and beyond.
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- Journal of Neurochemistry, 2016, v. 139, p. 91, doi. 10.1111/jnc.13266
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- Article
Leucine-rich repeat kinase 2 interacts with p21-activated kinase 6 to control neurite complexity in mammalian brain.
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- Journal of Neurochemistry, 2015, v. 135, n. 6, p. 1242, doi. 10.1111/jnc.13369
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- Article
Differential protein-protein interactions of LRRK1 and LRRK2 indicate roles in distinct cellular signaling pathways.
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- Journal of Neurochemistry, 2014, v. 131, n. 2, p. 239, doi. 10.1111/jnc.12798
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- Article
Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout mice.
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- Human Molecular Genetics, 2018, v. 27, n. 18, p. 3257, doi. 10.1093/hmg/ddy232
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- Article
LRRK2 phosphorylates membrane-bound Rabs and is activated by GTP-bound Rab7L1 to promote recruitment to the trans-Golgi network.
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- Human Molecular Genetics, 2018, v. 27, n. 2, p. 385, doi. 10.1093/hmg/ddx410
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- Article
Hexokinases link DJ-1 to the PINK1/parkin pathway.
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- Molecular Neurodegeneration, 2017, v. 12, p. 1, doi. 10.1186/s13024-017-0212-x
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- Article
DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy.
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- Human Molecular Genetics, 2011, v. 20, n. 1, p. 40, doi. 10.1093/hmg/ddq430
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- Article
Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
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- Human Molecular Genetics, 2005, v. 14, n. 23, p. 3661, doi. 10.1093/hmg/ddi394
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- Article
Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element.
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- Human Molecular Genetics, 2004, v. 13, n. 5, p. 543, doi. 10.1093/hmg/ddh053
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- Article
Association of a common genetic variant with Parkinson's disease is mediated by microglia.
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- Science Translational Medicine, 2022, v. 14, n. 655, p. 1, doi. 10.1126/scitranslmed.abp8869
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- Article
Mutations in LRRK2/dardarin associated with Parkinson disease are more toxic than equivalent mutations in the homologous kinase LRRK1.
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- Journal of Neurochemistry, 2007, v. 102, n. 1, p. 93, doi. 10.1111/j.1471-4159.2007.04523.x
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- Article
Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease.
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- Journal of Neurochemistry, 2005, v. 93, n. 1, p. 246, doi. 10.1111/j.1471-4159.2005.03019.x
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- Article
Cell population-specific expression analysis of human cerebellum.
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- BMC Genomics, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2164-13-610
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- Article