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Trends in Glucocerebrosides Research: A Systematic Review.
- Published in:
- Frontiers in Physiology, 2020, v. 11, p. N.PAG, doi. 10.3389/fphys.2020.558090
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- Publication type:
- Article
Genetic studies on chromosome 12 in late-onset Alzheimer disease.
- Published in:
- 1998
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- Publication type:
- journal article
PAK6 Phosphorylates 14-3-3γ to Regulate Steady State Phosphorylation of LRRK2.
- Published in:
- Frontiers in Molecular Neuroscience, 2017, p. 1, doi. 10.3389/fnmol.2017.00417
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- Publication type:
- Article
The C-Terminal Domain of LRRK2 with the G2019S Substitution Increases Mutant A53T α-Synuclein Toxicity in Dopaminergic Neurons In Vivo.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6760, doi. 10.3390/ijms22136760
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- Publication type:
- Article
Centrosomal cohesion deficits as cellular biomarker in lymphoblastoid cell lines from LRRK2 Parkinson's disease patients.
- Published in:
- Biochemical Journal, 2019, v. 476, n. 19, p. 2797, doi. 10.1042/BCJ20190315
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- Publication type:
- Article
Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00321
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- Publication type:
- Article
PARKINSON’S DISEASE-ASSOCIATED MUTATIONS IN LRRK2 CAUSE CENTROSOMAL DEFECTS VIA RAB8A PHOSPHORYLATION.
- Published in:
- 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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- Publication type:
- Article
P1-311: APOE locus and survival in a French cohort of demented cases
- Published in:
- 2006
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- Publication type:
- Abstract
P1-311: APOE locus and survival in a French cohort of demented cases
- Published in:
- 2006
- By:
- Publication type:
- Abstract
α-2 macroglobulin gene and Alzheimer disease.
- Published in:
- Nature Genetics, 1999, v. 22, n. 1, p. 17, doi. 10.1038/8726
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- Publication type:
- Article
The Current State-of-the Art of LRRK2-Based Biomarker Assay Development in Parkinson's Disease.
- Published in:
- Frontiers in Neuroscience, 2020, p. N.PAG, doi. 10.3389/fnins.2020.00865
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- Publication type:
- Article
LRRK2 Phosphorylation, More Than an Epiphenomenon.
- Published in:
- Frontiers in Neuroscience, 2020, v. 14, p. 1, doi. 10.3389/fnins.2020.00527
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- Publication type:
- Article
Transcriptomic signatures of brain regional vulnerability to Parkinson's disease.
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- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0804-9
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- Publication type:
- Article
Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease.
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- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 6, p. 661, doi. 10.1001/jama.296.6.661
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- Publication type:
- Article
In silico and Wet Bench Interactomics Sheds Light on the Similitudes and Differences between Human ROCO Proteins.
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- Proteomics, 2018, v. 18, n. 13, p. 1, doi. 10.1002/pmic.201800103
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- Publication type:
- Article
Apolipoprotein E in Guamanian amyotrophic lateral sclerosis/ parkinsonism-dementia complex: genotype analysis and relationships to neuropathological changes.
- Published in:
- Acta Neuropathologica, 1996, v. 91, n. 3, p. 247, doi. 10.1007/s004010050422
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- Publication type:
- Article
Alterations in the LRRK2-Rab pathway in urinary extracellular vesicles as Parkinson's disease and pharmacodynamic biomarkers.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00445-9
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- Publication type:
- Article
Alterations in the LRRK2-Rab pathway in urinary extracellular vesicles as Parkinson's disease and pharmacodynamic biomarkers.
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00445-9
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- Publication type:
- Article
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
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- Annals of Neurology, 2022, v. 92, n. 2, p. 270, doi. 10.1002/ana.26416
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- Publication type:
- Article
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
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- Annals of Neurology, 2011, v. 69, n. 5, p. 778, doi. 10.1002/ana.22321
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- Publication type:
- Article
Genomic investigation of α-synuclein multiplication and parkinsonism.
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- Annals of Neurology, 2008, v. 63, n. 6, p. 743, doi. 10.1002/ana.21380
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- Publication type:
- Article
GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2.
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- Human Molecular Genetics, 2017, v. 26, n. 14, p. 2747, doi. 10.1093/hmg/ddx161
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- Publication type:
- Article
LRRK2 detection in human biofluids: potential use as a Parkinson's disease biomarker?
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- Biochemical Society Transactions, 2017, v. 45, n. 1, p. 207, doi. 10.1042/BST20160334
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- Publication type:
- Article
Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson′s Disease.
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- Movement Disorders, 2022, v. 37, n. 8, p. 1761, doi. 10.1002/mds.29124
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- Publication type:
- Article
Crosstalk between the Hippo Pathway and the Wnt Pathway in Huntington's Disease and Other Neurodegenerative Disorders.
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- Cells (2073-4409), 2022, v. 11, n. 22, p. 3631, doi. 10.3390/cells11223631
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- Publication type:
- Article
A Phosphosite Mutant Approach on LRRK2 Links Phosphorylation and Dephosphorylation to Protective and Deleterious Markers, Respectively.
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- Cells (2073-4409), 2022, v. 11, n. 6, p. 1018, doi. 10.3390/cells11061018
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- Publication type:
- Article
Alpha-Synuclein and Lipids: The Elephant in the Room?
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- Cells (2073-4409), 2021, v. 10, n. 9, p. 2452, doi. 10.3390/cells10092452
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- Publication type:
- Article
Mind the Gap: LRRK2 Phenotypes in the Clinic vs. in Patient Cells.
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- Cells (2073-4409), 2021, v. 10, n. 5, p. 981, doi. 10.3390/cells10050981
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- Publication type:
- Article
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.
- Published in:
- Molecular Neurodegeneration, 2018, v. 13, p. 1, doi. 10.1186/s13024-018-0235-y
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- Publication type:
- Article
NADPH oxidases in Parkinson's disease: a systematic review.
- Published in:
- Molecular Neurodegeneration, 2017, v. 12, p. 1, doi. 10.1186/s13024-017-0225-5
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- Publication type:
- Article
Therapeutic potential of autophagy-enhancing agents in Parkinson's disease.
- Published in:
- Molecular Neurodegeneration, 2017, v. 12, p. 1, doi. 10.1186/s13024-017-0154-3
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- Publication type:
- Article
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.
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- Human Mutation, 2011, v. 32, n. 4, p. E2079, doi. 10.1002/humu.21459
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- Publication type:
- Article
Association between Parkinson’s disease and polymorphisms in the nNOS and iNOS genes in a community-based case–control study.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 1, p. 79, doi. 10.1093/hmg/ddg009
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- Publication type:
- Article
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.
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- Human Molecular Genetics, 2000, v. 9, n. 15, p. 2275, doi. 10.1093/oxfordjournals.hmg.a018918
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- Publication type:
- Article
Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM Study.
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- Human Molecular Genetics, 2000, v. 9, n. 1, p. 57, doi. 10.1093/hmg/9.1.57
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- Publication type:
- Article
A Novel Presenilin-2 Splice Variant in Human Alzheimer's Disease BrainTissue.
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- Journal of Neurochemistry, 1999, v. 72, n. 6, p. 2498, doi. 10.1046/j.1471-4159.1999.0722498.x
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- Publication type:
- Article
Alpha-synuclein repeat variants and survival in Parkinson's disease.
- Published in:
- Movement Disorders, 2014, v. 29, n. 8, p. 1053, doi. 10.1002/mds.25841
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- Publication type:
- Article
Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium.
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- Movement Disorders, 2013, v. 28, n. 12, p. 1740, doi. 10.1002/mds.25600
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- Publication type:
- Article
S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: Evidence for an age-dependent relationship.
- Published in:
- Movement Disorders, 2003, v. 18, n. 2, p. 130, doi. 10.1002/mds.10326
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- Publication type:
- Article
Linkage exclusion in French families with probable Parkinson's disease.
- Published in:
- Movement Disorders, 2000, v. 15, n. 6, p. 1075, doi. 10.1002/1531-8257(200011)15:6<1075::AID-MDS1004>3.0.CO;2-2
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- Publication type:
- Article
A full genome scan for late onset Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 2, p. 237, doi. 10.1093/hmg/8.2.237
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- Publication type:
- Article
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 9, p. 1511, doi. 10.1093/hmg/7.9.1511
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- Publication type:
- Article
A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's Disease.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 3, p. 533, doi. 10.1093/hmg/7.3.533
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- Publication type:
- Article
Distortion of Allelic Expression of Apolipoprotein E in Alzheimer's Disease.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2151, doi. 10.1093/hmg/6.12.2151
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- Publication type:
- Article
Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 3, p. 165
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- Publication type:
- Article
Glycosphingolipids and neuroinflammation in Parkinson's disease.
- Published in:
- Molecular Neurodegeneration, 2020, v. 15, n. 1, p. N.PAG, doi. 10.1186/s13024-020-00408-1
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- Publication type:
- Article