851 - 875 of 6230 Results
Title
Year
- Cognitive Profiles in Parkinson’s Disease and Their Relation to Dementia: A Data-Driven Approach2012OPENTitle: Cognitive Profiles in Parkinson’s Disease and Their Relation to Dementia: A Data-Driven ApproachJournal Name: International Journal of Alzheimer's DiseasePublisher: Hindawi LimitedVol: 2012Issue #:Start Page: 1End Page: 11Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1155/2012/910757Best OA location URL: https://downloads.hindawi.com/journals/ijad/2012/910757.pdfCitation Count: 12
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OPENTitle: KIF6 719Arg Carrier Status Association with Homocysteine and C-Reactive Protein in Amnestic Mild Cognitive Impairment and Alzheimer’s Disease PatientsJournal Name: International Journal of Alzheimer's DiseasePublisher: WileyVol: 2013Issue #:Start Page: 1End Page: 6Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1155/2013/242303Best OA location URL: https://downloads.hindawi.com/journals/ijad/2013/242303.pdfCitation Count: 3
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OPENTitle: Temporal Expression of Mutant LRRK2 in Adult Rats Impairs Dopamine ReuptakeJournal Name: International Journal of Biological SciencesPublisher: Ivyspring International PublisherVol: 7Issue #: 6Start Page: 753End Page: 761Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.7150/ijbs.7.753Best OA location URL: https://www.ijbs.com/v07p0753.pdfCitation Count: 58
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OPENTitle: Domain‐specific cognitive impairment in non‐demented Parkinson's disease psychosisJournal Name: International Journal of Geriatric PsychiatryPublisher: WileyVol: 33Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/gps.4736Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/5698175Citation Count: 10
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OPENTitle: Anosognosia increases caregiver burden in mild cognitive impairmentJournal Name: International Journal of Geriatric PsychiatryPublisher: WileyVol: 31Issue #: 7Start Page: 799End Page: 808Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/gps.4394Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8483618Citation Count: 48
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OPENTitle: Förster Resonance Energy Transfer (FRET) Correlates of Altered Subunit Stoichiometry in Cys-Loop Receptors, Exemplified by Nicotinic α4β2Journal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 13Issue #: 8Start Page: 10022End Page: 10040Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/ijms130810022Best OA location URL: https://www.mdpi.com/1422-0067/13/8/10022/pdf?version=1403144658Citation Count: 25
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OPENTitle: Pesticides that inhibit the ubiquitin–proteasome system: Effect measure modification by genetic variation in SKP1 in Parkinson׳s diseaseJournal Name: Environmental ResearchPublisher: Elsevier BVVol: 126Issue #:Start Page: 1End Page: 8Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.envres.2013.08.001Best OA location URL: http://doi.org/10.1016/j.envres.2013.08.001Citation Count: 48
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OPENTitle: Genetic variability at the PARK16 locusJournal Name: European Journal of Human GeneticsPublisher: Springer Science and Business Media LLCVol: 18Issue #: 12Start Page: 1356End Page: 1359Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/ejhg.2010.125Best OA location URL: https://www.nature.com/articles/ejhg2010125.pdfCitation Count: 91
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OPENTitle: Identification of candidate genes for familial early-onset essential tremorJournal Name: European Journal of Human GeneticsPublisher: Springer Science and Business Media LLCVol: 24Issue #: 7Start Page: 1009End Page: 1015Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/ejhg.2015.228Best OA location URL: https://www.nature.com/articles/ejhg2015228.pdfCitation Count: 39
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OPENTitle: A novel homozygous KY variant causing a complex neurological disorderJournal Name: European Journal of Medical GeneticsPublisher: Elsevier BVVol: 63Issue #: 11Start Page: 104031End Page: 104031Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.ejmg.2020.104031Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7554104Citation Count: 5
- LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP62012OPENTitle: LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 21Issue #: 22Start Page: 4966End Page: 4979Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/dds342Best OA location URL: https://academic.oup.com/hmg/article-pdf/21/22/4966/17257652/dds342.pdfCitation Count: 99
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OPENTitle: Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 21Issue #: 15Start Page: 3500End Page: 3512Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/dds161Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3392107Citation Count: 223
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OPENTitle: LRRK2 secretion in exosomes is regulated by 14-3-3Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 22Issue #: 24Start Page: 4988End Page: 5000Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddt346Best OA location URL: https://academic.oup.com/hmg/article-pdf/22/24/4988/14140078/ddt346.pdfCitation Count: 161
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OPENTitle: In vitro-differentiated neural cell cultures progress towards donor-identical brain tissueJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 22Issue #: 17Start Page: 3534End Page: 3546Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddt208Citation Count: 23
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OPENTitle: Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamilyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 8Start Page: 2055End Page: 2077Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddt600Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/8/2055/14143078/ddt600.pdfCitation Count: 124
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OPENTitle: Membrane recruitment of endogenous LRRK2 precedes its potent regulation of autophagyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 16Start Page: 4201End Page: 4214Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu138Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/16/4201/1737006/ddu138.pdfCitation Count: 220
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OPENTitle: Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegenerationJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 17Start Page: 4621End Page: 4638Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu178Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/17/4621/2215861/ddu178.pdfCitation Count: 148
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OPENTitle: Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 17Start Page: 4693End Page: 4702Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu158Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/17/4693/2193406/ddu158.pdfCitation Count: 61
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OPENTitle: Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: ddw348End Page: ddw348Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddw348Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/24/5483/10408585/ddw348.pdfCitation Count: 50
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OPENTitle: LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in DrosophilaJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 26Issue #: 7Start Page: 1247End Page: 1257Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddx030Best OA location URL: https://academic.oup.com/hmg/article-pdf/26/7/1247/25421311/ddx030.pdfCitation Count: 21
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OPENTitle: mGlu5positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndromeJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 25Issue #: 10Start Page: 1990End Page: 2004Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddw074Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/10/1990/18527444/ddw074.pdfCitation Count: 56
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OPENTitle: NEDD4-mediated HSF1 degradation underlies α-synucleinopathyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 25Issue #: 2Start Page: 211End Page: 222Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddv445Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/2/211/18526601/ddv445.pdfCitation Count: 84
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OPENTitle: GTP binding regulates cellular localization of Parkinson's disease-associated LRRK2Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 26Issue #: 14Start Page: 2747End Page: 2767Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddx161Best OA location URL: https://academic.oup.com/hmg/article-pdf/26/14/2747/24340312/ddx161.pdfCitation Count: 77
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OPENTitle: Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron diseaseJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: ddw429End Page: ddw429Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddw429Best OA location URL: https://academic.oup.com/hmg/article-pdf/26/4/ddw429/25332052/ddw429.pdfCitation Count: 86
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OPENTitle: LRRK2 G2019S-induced mitochondrial DNA damage is LRRK2 kinase dependent and inhibition restores mtDNA integrity in Parkinson’s diseaseJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 26Issue #: 22Start Page: 4340End Page: 4351Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddx320Best OA location URL: https://academic.oup.com/hmg/article-pdf/26/22/4340/24339268/ddx320.pdfCitation Count: 90