3141 - 3150 of 8620 Results
Title
Year
- Binding to serine 65‐phosphorylated ubiquitin primes Parkin for optimal PINK 1‐dependent phosphorylation and activation2015OPENTitle: Binding to serine 65‐phosphorylated ubiquitin primes Parkin for optimal PINK 1‐dependent phosphorylation and activationJournal Name: EMBO reportsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 8Start Page: 939End Page: 954Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/embr.201540352Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/embr.201540352Citation Count: 227
- Pesticides that inhibit the ubiquitin–proteasome system: Effect measure modification by genetic variation in SKP1 in Parkinson׳s disease2013OPENTitle: 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
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OPENTitle: Coffee, ADORA2A, and CYP1A2: the caffeine connection in Parkinson’s diseaseJournal Name: European Journal of NeurologyPublisher: WileyVol: 18Issue #: 5Start Page: 756End Page: 765Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/j.1468-1331.2011.03353.xBest OA location URL: https://europepmc.org/articles/pmc3556904?pdf=renderCitation Count: 112
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OPENTitle: Lack of evidence for an association between UCHL1 S18Y and Parkinson’s diseaseJournal Name: European Journal of NeurologyPublisher: WileyVol: 15Issue #: 2Start Page: 134End Page: 139Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/j.1468-1331.2007.02012.xBest OA location URL: http://doi.org/10.1111/j.1468-1331.2007.02012.xCitation Count: 31
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OPENTitle: Pure hereditary spastic paraplegia due to a de novo mutation in the NIPA1 geneJournal Name: European Journal of NeurologyPublisher: WileyVol: 21Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/ene.12284Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4138605Citation Count: 8
- Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis2014OPENTitle: Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosisJournal Name: European Journal of NeurologyPublisher: WileyVol: 22Issue #: 2Start Page: 328End Page: 333Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/ene.12572Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4289423Citation Count: 47
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OPENTitle: Genetic analysis of the FUS/TLS gene in essential tremorJournal Name: European Journal of NeurologyPublisher: WileyVol: 20Issue #: 3Start Page: 534End Page: 539Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/ene.12023Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4862621Citation Count: 35