{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T12:21:09Z","timestamp":1761740469358},"reference-count":30,"publisher":"Elsevier BV","issue":"1-2","license":[{"start":{"date-parts":[[2007,9,1]],"date-time":"2007-09-01T00:00:00Z","timestamp":1188604800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Physiology &amp; Behavior"],"published-print":{"date-parts":[[2007,9]]},"DOI":"10.1016\/j.physbeh.2007.05.046","type":"journal-article","created":{"date-parts":[[2007,5,25]],"date-time":"2007-05-25T12:23:21Z","timestamp":1180095801000},"page":"46-53","source":"Crossref","is-referenced-by-count":21,"title":["DJ-1 and UCH-L1 gene activity patterns in the brains of controls, Parkinson and schizophrenia patients and in rodents"],"prefix":"10.1016","volume":"92","author":[{"given":"Dagmar","family":"Galter","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marie","family":"Westerlund","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrea Carmine","family":"Belin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lars","family":"Olson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.physbeh.2007.05.046_bib1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1749-6632.2003.tb07458.x","article-title":"Description of Parkinson's disease as a clinical syndrome","volume":"991","author":"Fahn","year":"2003","journal-title":"Ann N Y Acad Sci"},{"key":"10.1016\/j.physbeh.2007.05.046_bib2","doi-asserted-by":"crossref","first-page":"605","DOI":"10.1038\/33416","article-title":"Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism","volume":"392","author":"Kitada","year":"1998","journal-title":"Nature"},{"key":"10.1016\/j.physbeh.2007.05.046_bib3","doi-asserted-by":"crossref","first-page":"629","DOI":"10.1086\/322996","article-title":"Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36","volume":"69","author":"van Duijn","year":"2001","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.physbeh.2007.05.046_bib4","doi-asserted-by":"crossref","first-page":"1158","DOI":"10.1126\/science.1096284","article-title":"Hereditary early-onset Parkinson's disease caused by mutations in PINK1","volume":"304","author":"Valente","year":"2004","journal-title":"Science"},{"key":"10.1016\/j.physbeh.2007.05.046_bib5","doi-asserted-by":"crossref","first-page":"1271","DOI":"10.1093\/brain\/awg136","article-title":"Parkin mutations are frequent in patients with isolated early-onset parkinsonism","volume":"126","author":"Periquet","year":"2003","journal-title":"Brain"},{"key":"10.1016\/j.physbeh.2007.05.046_bib6","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1002\/ana.10675","article-title":"The role of pathogenic DJ-1 mutations in Parkinson's disease","volume":"54","author":"Abou-Sleiman","year":"2003","journal-title":"Ann Neurol"},{"key":"10.1016\/j.physbeh.2007.05.046_bib7","doi-asserted-by":"crossref","first-page":"22","DOI":"10.1136\/jmg.2003.011106","article-title":"DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function","volume":"41","author":"Lockhart","year":"2004","journal-title":"J Med Genet"},{"key":"10.1016\/j.physbeh.2007.05.046_bib8","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1006\/bbrc.1997.6132","article-title":"DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras","volume":"231","author":"Nagakubo","year":"1997","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.physbeh.2007.05.046_bib9","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1002\/(SICI)1097-4644(19990301)72:3<435::AID-JCB12>3.0.CO;2-H","article-title":"Identification and characterization of a novel protein that regulates RNA-protein interaction","volume":"72","author":"Hod","year":"1999","journal-title":"J Cell Biochem"},{"key":"10.1016\/j.physbeh.2007.05.046_bib10","doi-asserted-by":"crossref","first-page":"37556","DOI":"10.1074\/jbc.M101730200","article-title":"DJ-1 positively regulates the androgen receptor by impairing the binding of PIASx alpha to the receptor","volume":"276","author":"Takahashi","year":"2001","journal-title":"J Biol Chem"},{"key":"10.1016\/j.physbeh.2007.05.046_bib11","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1038\/sj.embor.7400074","article-title":"DJ-1 has a role in antioxidative stress to prevent cell death","volume":"5","author":"Taira","year":"2004","journal-title":"EMBO J"},{"key":"10.1016\/j.physbeh.2007.05.046_bib12","doi-asserted-by":"crossref","first-page":"1342","DOI":"10.1016\/j.bbrc.2003.11.056","article-title":"Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition","volume":"312","author":"Yokota","year":"2003","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.physbeh.2007.05.046_bib13","doi-asserted-by":"crossref","first-page":"420","DOI":"10.1093\/brain\/awh054","article-title":"The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease","volume":"127","author":"Bandopadhyay","year":"2004","journal-title":"Brain"},{"key":"10.1016\/j.physbeh.2007.05.046_bib14","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1038\/26652","article-title":"The ubiquitin pathway in Parkinson's disease","volume":"395","author":"Leroy","year":"1998","journal-title":"Nature"},{"key":"10.1016\/j.physbeh.2007.05.046_bib15","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1002\/ana.20017","article-title":"UCHL-1 is a Parkinson's disease susceptibility gene","volume":"55","author":"Maraganore","year":"2004","journal-title":"Ann Neurol"},{"key":"10.1016\/j.physbeh.2007.05.046_bib16","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/S0022-510X(01)00555-X","article-title":"A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population","volume":"189","author":"Satoh","year":"2001","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.physbeh.2007.05.046_bib17","doi-asserted-by":"crossref","first-page":"670","DOI":"10.1126\/science.2530630","article-title":"The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase","volume":"246","author":"Wilkinson","year":"1989","journal-title":"Science"},{"key":"10.1016\/j.physbeh.2007.05.046_bib18","doi-asserted-by":"crossref","first-page":"6735","DOI":"10.1021\/bi960099f","article-title":"Substrate binding and catalysis by ubiquitin C-terminal hydrolases: identification of two active site residues","volume":"35","author":"Larsen","year":"1996","journal-title":"Biochemistry"},{"key":"10.1016\/j.physbeh.2007.05.046_bib19","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1007\/BF00716936","article-title":"Sensitive mRNA detection using unfixed tissue: combined radioactive and non-radioactive in situ hybridization histochemistry","volume":"98","author":"Dagerlind","year":"1992","journal-title":"Histochemistry"},{"key":"10.1016\/j.physbeh.2007.05.046_bib20","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1016\/j.nbd.2003.09.001","article-title":"ALDH1 mRNA: presence in human dopamine neurons and decreases in substantia nigra in Parkinson's disease and in the ventral tegmental area in schizophrenia","volume":"14","author":"Galter","year":"2003","journal-title":"Neurobiol Dis"},{"key":"10.1016\/j.physbeh.2007.05.046_bib21","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1002\/1531-8249(200002)47:2<201::AID-ANA10>3.0.CO;2-F","article-title":"Expression of alpha-synuclein, parkin, and ubiquitin carboxy-terminal hydrolase L1 mRNA in human brain: genes associated with familial Parkinson's disease","volume":"47","author":"Solano","year":"2000","journal-title":"Ann Neurol"},{"issue":"Suppl 2","key":"10.1016\/j.physbeh.2007.05.046_bib22","doi-asserted-by":"crossref","first-page":"II3","DOI":"10.1007\/PL00007758","article-title":"Pathoanatomy of Parkinson's disease","volume":"247","author":"Braak","year":"2000","journal-title":"J Neurol"},{"key":"10.1016\/j.physbeh.2007.05.046_bib23","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1007\/s00401-004-0834-2","article-title":"Pathological properties of the Parkinson's disease-associated protein DJ-1 in alpha-synucleinopathies and tauopathies: relevance for multiple system atrophy and Pick's disease","volume":"107","author":"Neumann","year":"2004","journal-title":"Acta Neuropathol"},{"key":"10.1016\/j.physbeh.2007.05.046_bib24","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1002\/ana.10782","article-title":"DJ-1 colocalizes with tau inclusions: a link between parkinsonism and dementia","volume":"55","author":"Rizzu","year":"2004","journal-title":"Ann Neurol"},{"key":"10.1016\/j.physbeh.2007.05.046_bib25","doi-asserted-by":"crossref","first-page":"8506","DOI":"10.1074\/jbc.M311017200","article-title":"Familial Parkinson's disease-associated L166P mutation disrupts DJ-1 protein folding and function","volume":"279","author":"Olzmann","year":"2004","journal-title":"J Biol Chem"},{"key":"10.1016\/j.physbeh.2007.05.046_bib26","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1016\/j.neulet.2004.06.002","article-title":"Localization of DJ-1 mRNA in the mouse brain","volume":"367","author":"Shang","year":"2004","journal-title":"Neurosci Lett"},{"key":"10.1016\/j.physbeh.2007.05.046_bib27","doi-asserted-by":"crossref","first-page":"256","DOI":"10.1126\/science.1077209","article-title":"Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism","volume":"299","author":"Bonifati","year":"2003","journal-title":"Science"},{"key":"10.1016\/j.physbeh.2007.05.046_bib28","doi-asserted-by":"crossref","first-page":"31372","DOI":"10.1074\/jbc.M304221200","article-title":"Crystal structure of human DJ-1, a protein associated with early onset Parkinson's disease","volume":"278","author":"Tao","year":"2003","journal-title":"J Biol Chem"},{"key":"10.1016\/j.physbeh.2007.05.046_bib29","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/S0014-5793(03)00764-6","article-title":"Crystal structure of DJ-1\/RS and implication on familial Parkinson's disease","volume":"549","author":"Huai","year":"2003","journal-title":"FEBS Lett"},{"key":"10.1016\/j.physbeh.2007.05.046_bib30","doi-asserted-by":"crossref","first-page":"6943","DOI":"10.1074\/jbc.M309204200","article-title":"Differential effects of Parkinson's disease-associated mutations on stability and folding of DJ-1","volume":"279","author":"Gorner","year":"2004","journal-title":"J Biol Chem"}],"container-title":["Physiology &amp; Behavior"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031938407001953?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0031938407001953?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,7]],"date-time":"2019-01-07T04:26:42Z","timestamp":1546835202000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0031938407001953"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,9]]},"references-count":30,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2007,9]]}},"alternative-id":["S0031938407001953"],"URL":"https:\/\/doi.org\/10.1016\/j.physbeh.2007.05.046","relation":{},"ISSN":["0031-9384"],"issn-type":[{"value":"0031-9384","type":"print"}],"subject":[],"published":{"date-parts":[[2007,9]]}}}