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

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

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

Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin geneKUNISHIGE, Makoto; MITSUI, Takao; KURODA, Yukiko et al.European neurology. 2004, Vol 51, Num 3, pp 183-185, issn 0014-3022, 3 p.Article

Does parkin play a role in the peripheral nervous system? A family reportABBRUZZESE, Giovanni; PIGULLO, Simona; AJMAR, Franco et al.Movement disorders. 2004, Vol 19, Num 8, pp 978-981, issn 0885-3185, 4 p.Article

Mitophagy and Disease: New Avenues for Pharmacological InterventionTAYLOR, Robert; GOLDMAN, Scott J.Current pharmaceutical design (Print). 2011, Vol 17, Num 20, pp 2056-2073, issn 1381-6128, 18 p.Article

Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsKAY, Denise M; MORAN, Dawn; SCHELLENBERG, Gerard D et al.Annals of neurology. 2007, Vol 61, Num 1, pp 47-54, issn 0364-5134, 8 p.Article

Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers A TMS studyBAUMER, T; PRAMSTALLER, P. P; SIEBNER, H. R et al.Neurology. 2007, Vol 69, Num 21, pp 1976-1981, issn 0028-3878, 6 p.Article

P32 REGULATES MITOCHONDRIAL MORPHOLOGY AND DYNAMICS THROUGH PARKINLI, Y; WAN, O. W; XIE, W et al.Neuroscience. 2011, Vol 199, pp 346-358, issn 0306-4522, 13 p.Article

Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2 : An FP-CIT SPECT studyPELLECCHIA, Maria Teresa; VARRONE, Andrea; QUATTRONE, Aldo et al.Movement disorders. 2007, Vol 22, Num 4, pp 559-563, issn 0885-3185, 5 p.Article

Mutation of the parkin gene in a persian family : Clinical progression over a 40-year periodCLARIMON, Jordi; JOHNSON, Janel; DJALDETTI, Ruth et al.Movement disorders. 2005, Vol 20, Num 7, pp 887-890, issn 0885-3185, 4 p.Article

Defining the breakpoints of the Quaking^viable mouse mutation reveals a duplication from a Parkin intronDAPPER, Jason D; JUSTICE, Monica J.Movement disorders. 2005, Vol 20, Num 10, pp 1369-1374, issn 0885-3185, 6 p.Article