Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association
We provided data to show that the transcriptional activity of wildtype -258T in the parkin promoter region was significantly higher than the -258G variant in human cell lines. The transcriptional activity of wildtype -258T was significantly increased under oxidative stress by hydrogen peroxide, but...
Gespeichert in:
Veröffentlicht in: | Human genetics 2005-12, Vol.118 (3-4), p.484-488 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 488 |
---|---|
container_issue | 3-4 |
container_start_page | 484 |
container_title | Human genetics |
container_volume | 118 |
creator | TAN, E. K PUONG, K. Y WONG, M. C PUVAN, K ZHAO, Y CHAN, D. K. Y YEW, K FOOK-CHONG, S SHEN, H NG, P. W WOO, J YUEN, Y PAVANNI, R |
description | We provided data to show that the transcriptional activity of wildtype -258T in the parkin promoter region was significantly higher than the -258G variant in human cell lines. The transcriptional activity of wildtype -258T was significantly increased under oxidative stress by hydrogen peroxide, but this was not observed for the -258G variant. The transcriptional upregulation was significantly higher for wildtype -258T compared to -258G variant at 0.1, 0.2 and 0.4 mM of hydrogen peroxide. Similar results were obtained when the cells were treated with a proteasome inhibitor, MG132.Furthermore, in a case control study involving 753 subjects, we demonstrated that the parkin promoter -258G variant was associated with an increased risk of sporadic Parkinson's disease (PD) in the elderly ethnic Chinese population. Our clinical and laboratory data provide corroborative evidence that some older individuals who have the -258G variant may have a higher risk of developing PD. |
doi_str_mv | 10.1007/s00439-005-0038-4 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_746277391</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A791262630</galeid><sourcerecordid>A791262630</sourcerecordid><originalsourceid>FETCH-LOGICAL-c512t-4e399658e80c1052c7a965dec249a1dfb4d49874bb1dcfa3cdfe6403d6b103fe3</originalsourceid><addsrcrecordid>eNqFkt9uFCEUxonR2HX1AbwxE40aL0Y5wAyDd01TdZMmGv9cEwaYlToDW2Ca9hF8a5nuJk290AtCDvnx8XHOh9BTwG8BY_4uYcyoqDFuyqJdze6hFTBKaiCY3kcrTBmuWw78CD1K6RxjaARpHqIjaAljHW9W6Pdm2ikXralyVD7p6HbZBa_Gat5Fu51HtZRVGKovKv5yvtrFMIVsY3WpolM-V7M3pQpXzhT00lYpR5tSpbxZ2GxVClORc_6n692N2PtKj847XU5VSkG7mzceoweDGpN9ctjX6MeH0-8nn-qzzx83J8dntW6A5JpZKkTbdLbDGnBDNFelNFYTJhSYoWeGiY6zvgejB0W1GWzLMDVtD5gOlq7R671ucXcx25Tl5JK246i8DXOSnLWEcyqgkK_-SRLcEYI5-y8IomkFFl0Bn_8Fnoc5lm4XMWgaBlA8rtGLPbRVo5XOD6GMRi-K8pgLIC1p6UK9uUPp4LO9yls1pyQ3377eZWHP6hhSinaQu-gmFa8lYLkkSe6TJEuS5JIkufzp2cHq3E_W3N44RKcALw-ASmWUQ4mPdumWKy3sgAH9A8Ml0Xo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>215541110</pqid></control><display><type>article</type><title>Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association</title><source>MEDLINE</source><source>Springer Online Journals Complete</source><creator>TAN, E. K ; PUONG, K. Y ; WONG, M. C ; PUVAN, K ; ZHAO, Y ; CHAN, D. K. Y ; YEW, K ; FOOK-CHONG, S ; SHEN, H ; NG, P. W ; WOO, J ; YUEN, Y ; PAVANNI, R</creator><creatorcontrib>TAN, E. K ; PUONG, K. Y ; WONG, M. C ; PUVAN, K ; ZHAO, Y ; CHAN, D. K. Y ; YEW, K ; FOOK-CHONG, S ; SHEN, H ; NG, P. W ; WOO, J ; YUEN, Y ; PAVANNI, R</creatorcontrib><description>We provided data to show that the transcriptional activity of wildtype -258T in the parkin promoter region was significantly higher than the -258G variant in human cell lines. The transcriptional activity of wildtype -258T was significantly increased under oxidative stress by hydrogen peroxide, but this was not observed for the -258G variant. The transcriptional upregulation was significantly higher for wildtype -258T compared to -258G variant at 0.1, 0.2 and 0.4 mM of hydrogen peroxide. Similar results were obtained when the cells were treated with a proteasome inhibitor, MG132.Furthermore, in a case control study involving 753 subjects, we demonstrated that the parkin promoter -258G variant was associated with an increased risk of sporadic Parkinson's disease (PD) in the elderly ethnic Chinese population. Our clinical and laboratory data provide corroborative evidence that some older individuals who have the -258G variant may have a higher risk of developing PD.</description><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/s00439-005-0038-4</identifier><identifier>PMID: 16244875</identifier><identifier>CODEN: HUGEDQ</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Age Factors ; Aged ; Biological and medical sciences ; Case-Control Studies ; Cell Culture Techniques ; Cells ; China - ethnology ; Classical genetics, quantitative genetics, hybrids ; Female ; Fundamental and applied biological sciences. Psychology ; Genetic aspects ; Genetic Predisposition to Disease ; Genetic transcription ; Genetic Variation ; Genetics of eukaryotes. Biological and molecular evolution ; Hospitals ; Human ; Humans ; Hydrogen peroxide ; Hydrogen Peroxide - pharmacology ; Kinases ; Male ; Middle Aged ; Molecular and cellular biology ; Molecular genetics ; Older people ; Oxidants - pharmacology ; Oxidative Stress ; Parkinson Disease - ethnology ; Parkinson Disease - etiology ; Parkinson Disease - genetics ; Parkinson's disease ; Promoter Regions, Genetic ; Proteasome Inhibitors ; Risk factors ; Software ; Transcription, Genetic ; Transcription. Transcription factor. Splicing. Rna processing ; Ubiquitin-Protein Ligases - biosynthesis ; Ubiquitin-Protein Ligases - genetics ; Up-Regulation</subject><ispartof>Human genetics, 2005-12, Vol.118 (3-4), p.484-488</ispartof><rights>2006 INIST-CNRS</rights><rights>COPYRIGHT 2005 Springer</rights><rights>Springer-Verlag 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-4e399658e80c1052c7a965dec249a1dfb4d49874bb1dcfa3cdfe6403d6b103fe3</citedby><cites>FETCH-LOGICAL-c512t-4e399658e80c1052c7a965dec249a1dfb4d49874bb1dcfa3cdfe6403d6b103fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17398141$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16244875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAN, E. K</creatorcontrib><creatorcontrib>PUONG, K. Y</creatorcontrib><creatorcontrib>WONG, M. C</creatorcontrib><creatorcontrib>PUVAN, K</creatorcontrib><creatorcontrib>ZHAO, Y</creatorcontrib><creatorcontrib>CHAN, D. K. Y</creatorcontrib><creatorcontrib>YEW, K</creatorcontrib><creatorcontrib>FOOK-CHONG, S</creatorcontrib><creatorcontrib>SHEN, H</creatorcontrib><creatorcontrib>NG, P. W</creatorcontrib><creatorcontrib>WOO, J</creatorcontrib><creatorcontrib>YUEN, Y</creatorcontrib><creatorcontrib>PAVANNI, R</creatorcontrib><title>Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association</title><title>Human genetics</title><addtitle>Hum Genet</addtitle><description>We provided data to show that the transcriptional activity of wildtype -258T in the parkin promoter region was significantly higher than the -258G variant in human cell lines. The transcriptional activity of wildtype -258T was significantly increased under oxidative stress by hydrogen peroxide, but this was not observed for the -258G variant. The transcriptional upregulation was significantly higher for wildtype -258T compared to -258G variant at 0.1, 0.2 and 0.4 mM of hydrogen peroxide. Similar results were obtained when the cells were treated with a proteasome inhibitor, MG132.Furthermore, in a case control study involving 753 subjects, we demonstrated that the parkin promoter -258G variant was associated with an increased risk of sporadic Parkinson's disease (PD) in the elderly ethnic Chinese population. Our clinical and laboratory data provide corroborative evidence that some older individuals who have the -258G variant may have a higher risk of developing PD.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Cell Culture Techniques</subject><subject>Cells</subject><subject>China - ethnology</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic aspects</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetic transcription</subject><subject>Genetic Variation</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Hospitals</subject><subject>Human</subject><subject>Humans</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Kinases</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Older people</subject><subject>Oxidants - pharmacology</subject><subject>Oxidative Stress</subject><subject>Parkinson Disease - ethnology</subject><subject>Parkinson Disease - etiology</subject><subject>Parkinson Disease - genetics</subject><subject>Parkinson's disease</subject><subject>Promoter Regions, Genetic</subject><subject>Proteasome Inhibitors</subject><subject>Risk factors</subject><subject>Software</subject><subject>Transcription, Genetic</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><subject>Ubiquitin-Protein Ligases - biosynthesis</subject><subject>Ubiquitin-Protein Ligases - genetics</subject><subject>Up-Regulation</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkt9uFCEUxonR2HX1AbwxE40aL0Y5wAyDd01TdZMmGv9cEwaYlToDW2Ca9hF8a5nuJk290AtCDvnx8XHOh9BTwG8BY_4uYcyoqDFuyqJdze6hFTBKaiCY3kcrTBmuWw78CD1K6RxjaARpHqIjaAljHW9W6Pdm2ikXralyVD7p6HbZBa_Gat5Fu51HtZRVGKovKv5yvtrFMIVsY3WpolM-V7M3pQpXzhT00lYpR5tSpbxZ2GxVClORc_6n692N2PtKj847XU5VSkG7mzceoweDGpN9ctjX6MeH0-8nn-qzzx83J8dntW6A5JpZKkTbdLbDGnBDNFelNFYTJhSYoWeGiY6zvgejB0W1GWzLMDVtD5gOlq7R671ucXcx25Tl5JK246i8DXOSnLWEcyqgkK_-SRLcEYI5-y8IomkFFl0Bn_8Fnoc5lm4XMWgaBlA8rtGLPbRVo5XOD6GMRi-K8pgLIC1p6UK9uUPp4LO9yls1pyQ3377eZWHP6hhSinaQu-gmFa8lYLkkSe6TJEuS5JIkufzp2cHq3E_W3N44RKcALw-ASmWUQ4mPdumWKy3sgAH9A8Ml0Xo</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>TAN, E. K</creator><creator>PUONG, K. Y</creator><creator>WONG, M. C</creator><creator>PUVAN, K</creator><creator>ZHAO, Y</creator><creator>CHAN, D. K. Y</creator><creator>YEW, K</creator><creator>FOOK-CHONG, S</creator><creator>SHEN, H</creator><creator>NG, P. W</creator><creator>WOO, J</creator><creator>YUEN, Y</creator><creator>PAVANNI, R</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope></search><sort><creationdate>20051201</creationdate><title>Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association</title><author>TAN, E. K ; PUONG, K. Y ; WONG, M. C ; PUVAN, K ; ZHAO, Y ; CHAN, D. K. Y ; YEW, K ; FOOK-CHONG, S ; SHEN, H ; NG, P. W ; WOO, J ; YUEN, Y ; PAVANNI, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-4e399658e80c1052c7a965dec249a1dfb4d49874bb1dcfa3cdfe6403d6b103fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Cell Culture Techniques</topic><topic>Cells</topic><topic>China - ethnology</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic aspects</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetic transcription</topic><topic>Genetic Variation</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Hospitals</topic><topic>Human</topic><topic>Humans</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Kinases</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Older people</topic><topic>Oxidants - pharmacology</topic><topic>Oxidative Stress</topic><topic>Parkinson Disease - ethnology</topic><topic>Parkinson Disease - etiology</topic><topic>Parkinson Disease - genetics</topic><topic>Parkinson's disease</topic><topic>Promoter Regions, Genetic</topic><topic>Proteasome Inhibitors</topic><topic>Risk factors</topic><topic>Software</topic><topic>Transcription, Genetic</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><topic>Ubiquitin-Protein Ligases - biosynthesis</topic><topic>Ubiquitin-Protein Ligases - genetics</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAN, E. K</creatorcontrib><creatorcontrib>PUONG, K. Y</creatorcontrib><creatorcontrib>WONG, M. C</creatorcontrib><creatorcontrib>PUVAN, K</creatorcontrib><creatorcontrib>ZHAO, Y</creatorcontrib><creatorcontrib>CHAN, D. K. Y</creatorcontrib><creatorcontrib>YEW, K</creatorcontrib><creatorcontrib>FOOK-CHONG, S</creatorcontrib><creatorcontrib>SHEN, H</creatorcontrib><creatorcontrib>NG, P. W</creatorcontrib><creatorcontrib>WOO, J</creatorcontrib><creatorcontrib>YUEN, Y</creatorcontrib><creatorcontrib>PAVANNI, R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><jtitle>Human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAN, E. K</au><au>PUONG, K. Y</au><au>WONG, M. C</au><au>PUVAN, K</au><au>ZHAO, Y</au><au>CHAN, D. K. Y</au><au>YEW, K</au><au>FOOK-CHONG, S</au><au>SHEN, H</au><au>NG, P. W</au><au>WOO, J</au><au>YUEN, Y</au><au>PAVANNI, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association</atitle><jtitle>Human genetics</jtitle><addtitle>Hum Genet</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>118</volume><issue>3-4</issue><spage>484</spage><epage>488</epage><pages>484-488</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><coden>HUGEDQ</coden><abstract>We provided data to show that the transcriptional activity of wildtype -258T in the parkin promoter region was significantly higher than the -258G variant in human cell lines. The transcriptional activity of wildtype -258T was significantly increased under oxidative stress by hydrogen peroxide, but this was not observed for the -258G variant. The transcriptional upregulation was significantly higher for wildtype -258T compared to -258G variant at 0.1, 0.2 and 0.4 mM of hydrogen peroxide. Similar results were obtained when the cells were treated with a proteasome inhibitor, MG132.Furthermore, in a case control study involving 753 subjects, we demonstrated that the parkin promoter -258G variant was associated with an increased risk of sporadic Parkinson's disease (PD) in the elderly ethnic Chinese population. Our clinical and laboratory data provide corroborative evidence that some older individuals who have the -258G variant may have a higher risk of developing PD.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><cop>New York, NY</cop><pub>Springer</pub><pmid>16244875</pmid><doi>10.1007/s00439-005-0038-4</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0340-6717 |
ispartof | Human genetics, 2005-12, Vol.118 (3-4), p.484-488 |
issn | 0340-6717 1432-1203 |
language | eng |
recordid | cdi_proquest_miscellaneous_746277391 |
source | MEDLINE; Springer Online Journals Complete |
subjects | Age Factors Aged Biological and medical sciences Case-Control Studies Cell Culture Techniques Cells China - ethnology Classical genetics, quantitative genetics, hybrids Female Fundamental and applied biological sciences. Psychology Genetic aspects Genetic Predisposition to Disease Genetic transcription Genetic Variation Genetics of eukaryotes. Biological and molecular evolution Hospitals Human Humans Hydrogen peroxide Hydrogen Peroxide - pharmacology Kinases Male Middle Aged Molecular and cellular biology Molecular genetics Older people Oxidants - pharmacology Oxidative Stress Parkinson Disease - ethnology Parkinson Disease - etiology Parkinson Disease - genetics Parkinson's disease Promoter Regions, Genetic Proteasome Inhibitors Risk factors Software Transcription, Genetic Transcription. Transcription factor. Splicing. Rna processing Ubiquitin-Protein Ligases - biosynthesis Ubiquitin-Protein Ligases - genetics Up-Regulation |
title | Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition : clinical association |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T16%3A21%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impaired%20transcriptional%20upregulation%20of%20Parkin%20promoter%20variant%20under%20oxidative%20stress%20and%20proteasomal%20inhibition%20:%20clinical%20association&rft.jtitle=Human%20genetics&rft.au=TAN,%20E.%20K&rft.date=2005-12-01&rft.volume=118&rft.issue=3-4&rft.spage=484&rft.epage=488&rft.pages=484-488&rft.issn=0340-6717&rft.eissn=1432-1203&rft.coden=HUGEDQ&rft_id=info:doi/10.1007/s00439-005-0038-4&rft_dat=%3Cgale_proqu%3EA791262630%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=215541110&rft_id=info:pmid/16244875&rft_galeid=A791262630&rfr_iscdi=true |