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Evidence for the presence of full-length PARK2 mRNA and Parkin protein in human bloodKASAP, Murat; AKPINAR, Gurler; SAZCI, Ali et al.Neuroscience letters. 2009, Vol 460, Num 3, pp 196-200, issn 0304-3940, 5 p.Article

Salubrinal protects against rotenone-induced SH-SY5Y cell death via ATF4-parkin pathwayLIANG WU; NA LUO; ZHAO, Hong-Rui et al.Brain research. 2014, Vol 1549, pp 52-62, issn 0006-8993, 11 p.Article

DJ-1, PINK 1, and Their Effects on Mitochondrial PathwaysCOOKSON, Mark R.Movement disorders. 2010, Vol 25, Num 3, issn 0885-3185, S44-S48, SUP1Conference Paper

Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonismMORO, E; VOLKMANN, J; VOGES, J et al.Neurology. 2008, Vol 70, Num 14, pp 1186-1191, issn 0028-3878, 6 p.Article

The Normal Parkin SequenceYONG REN; XIAOJUN LIU; LESAGE, Suzanne et al.Movement disorders. 2012, Vol 27, Num 3, pp 463-464, issn 0885-3185, 2 p.Article

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutationsPANKRATZ, N; KISSELL, D. K; PAUCIULO, M. W et al.Neurology. 2009, Vol 73, Num 4, pp 279-286, issn 0028-3878, 8 p.Article

Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD studyALCALAY, R. N; SIDEROWF, A; FAHN, S et al.Neurology. 2011, Vol 76, Num 4, pp 319-326, issn 0028-3878, 8 p.Article

Clinical findings in a large family with a parkin Ex3Δ40 mutationMUNHOZ, Renato P; SA, Daniel S; ROGAEVA, Ekaterina et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 701-704, issn 0003-9942, 4 p.Article

PINK1 gene knockdown leads to increased binding of parkin with actin filamentKIM, Kyung-Hee; SON, Jin H.Neuroscience letters. 2010, Vol 468, Num 3, pp 272-276, issn 0304-3940, 5 p.Article

Parkin is ubiquitinated by Nrdp1 and abrogates Nrdp1-induced oxidative stressFURONG YU; JIANHUA ZHOU.Neuroscience letters. 2008, Vol 440, Num 1, pp 4-8, issn 0304-3940, 5 p.Article

Parkin disease in a brazilian kindred : Manifesting heterozygotes and clinical follow-up over 10 yearsKHAN, Naheed L; HORTA, Wagner; EUNSON, Louise et al.Movement disorders. 2005, Vol 20, Num 4, pp 479-484, issn 0885-3185, 6 p.Article

A multidisciplinary study of patients with early-onset PD with and without parkin mutationsLOHMANN, E; THOBOIS, S; POLLAK, P et al.Neurology. 2009, Vol 72, Num 2, pp 110-116, issn 0028-3878, 7 p.Article

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotypeVAN NUENEN, B. F. L; WEISS, M. M; SIEBNER, H. R et al.Neurology. 2009, Vol 72, Num 12, pp 1041-1047, issn 0028-3878, 7 p.Article

Heterogeneous phenotype in a family with compound heterozygous parkin gene mutationsHAO DENG; LE, Wei-Dong; HUNTER, Christine B et al.Archives of neurology (Chicago). 2006, Vol 63, Num 2, pp 273-277, issn 0003-9942, 5 p.Article

Parkin Mutations and early-onset Parkinsonism in a Taiwanese cohortWU, Ruey-Meei; BOUNDS, Rebecca; LINCOLN, Sarah et al.Archives of neurology (Chicago). 2005, Vol 62, Num 1, pp 82-87, issn 0003-9942, 6 p.Article

Parkin-positive autosomal recessive juvenile parkinsonism with α-synuclein-positive inclusionsSASAKI, Shoichi; SHIRATA, Akiko; YAMANE, Kiyomi et al.Neurology. 2004, Vol 63, Num 4, pp 678-682, issn 0028-3878, 5 p.Article

Distribution, type, and origin of Parkin mutations: Review and case studiesHEDRICH, Katja; ESKELSON, Cordula; LANG, Anthony E et al.Movement disorders. 2004, Vol 19, Num 10, pp 1146-1157, issn 0885-3185, 12 p.Article

Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutationsMÜFTÜOGLU, Meltem; ELIBOL, Bülent; DALMIZRAK, Özlem et al.Movement disorders. 2004, Vol 19, Num 5, pp 544-548, issn 0885-3185, 5 p.Article

Mutation Analysis of Parkin, PINK1, DJ-1 and ATP13A2 Genes in Chinese Patients with Autosomal Recessive Early-Onset ParkinsonismGUO, Ji-Feng; BIN XIAO; YAN, Xin-Xiang et al.Movement disorders. 2008, Vol 23, Num 14, pp 2074-2079, issn 0885-3185, 6 p.Article

Mutational analysis of the PINK I gene in early-onset parkinsonism in Europe and North AfricaIBANEZ, Pablo; LESAGE, Suzanne; LOHMANN, Ebba et al.Brain. 2006, Vol 129, pp 686-694, issn 0006-8950, 9 p., 3Article

Genetic analysis of parkin co-regulated gene (PACRG) in patients with early-onset parkinsonismHAO DENG; LE, Wei-Dong; XIE, Wen-Jie et al.Neuroscience letters. 2005, Vol 382, Num 3, pp 297-299, issn 0304-3940, 3 p.Article

Eye movement disorders are different in Parkin-linked and idiopathic early-onset PDMACHNER, B; KLEIN, C; SPRENGER, A et al.Neurology. 2010, Vol 75, Num 2, pp 125-128, issn 0028-3878, 4 p.Article

Parkin polymorphisms in progressive supranuclear palsyROS, Raquel; AMPUERO, Israel; GARCIA DE YEBENES, Justo et al.Journal of the neurological sciences. 2008, Vol 268, Num 1-2, pp 176-178, issn 0022-510X, 3 p.Article

Mitochondrial Function and Morphology Are Impaired in parkin-Mutant FibroblastsMORTIBOYS, Heather; THOMAS, Kelly Jean; BANDMANN, Oliver et al.Annals of neurology. 2008, Vol 64, Num 5, pp 555-565, issn 0364-5134, 11 p.Article