Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese
The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic...
Saved in:
Published in | Neurobiology of aging Vol. 31; no. 12; pp. 2194 - 2196 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.12.2010
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (
UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the
UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528,
p
=
0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16,
p
=
0.88). A multivariate logistic regression analysis showed that family history,
UCHL1 variant and the interaction of
UCHL1 variant and age at onset (
p
=
0.816) were not significantly associated with PD. |
---|---|
AbstractList | The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (
UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the
UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528,
p
=
0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16,
p
=
0.88). A multivariate logistic regression analysis showed that family history,
UCHL1 variant and the interaction of
UCHL1 variant and age at onset (
p
=
0.816) were not significantly associated with PD. The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p = 0.816) were not significantly associated with PD. Abstract The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1 ) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p = 0.87, OR 1.01, 95% CI 0.92–1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84–1.16, p = 0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset ( p = 0.816) were not significantly associated with PD. The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p=0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p=0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p=0.816) were not significantly associated with PD.The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p=0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p=0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p=0.816) were not significantly associated with PD. |
Author | An, X.K. Burgunder, J.M. Wu, Y.R. Wu-Chou, Y.H. Lu, C.S. Tan, E.K. Tan, L.C. Fook-Chong, S. Weng, Y.H. Chen, C.M. Chen, R.S. Wu, R.M. Lee, M.C. Fung, H.C. Peng, R. Zhang, Z.J. Lee-Chen, G.J. Teo, Y.Y. |
Author_xml | – sequence: 1 givenname: E.K. surname: Tan fullname: Tan, E.K. email: gnrtek@sgh.com.sg organization: Departments of Neurology and Clinical Research, Singapore General Hospital, National Neuroscience Institute, Singapore – sequence: 2 givenname: C.S. surname: Lu fullname: Lu, C.S. organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 3 givenname: R. surname: Peng fullname: Peng, R. organization: Department of Neurology, West China Hospital, Sichuan University, Chengdu, China – sequence: 4 givenname: Y.Y. surname: Teo fullname: Teo, Y.Y. organization: Wellcome Trust Centre for Human Genetics, University of Oxford, UK – sequence: 5 givenname: Y.H. surname: Wu-Chou fullname: Wu-Chou, Y.H. organization: Human Molecular Genetics Laboratory, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 6 givenname: R.S. surname: Chen fullname: Chen, R.S. organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 7 givenname: Y.H. surname: Weng fullname: Weng, Y.H. organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 8 givenname: C.M. surname: Chen fullname: Chen, C.M. organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 9 givenname: H.C. surname: Fung fullname: Fung, H.C. organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan – sequence: 10 givenname: L.C. surname: Tan fullname: Tan, L.C. organization: Departments of Neurology and Clinical Research, Singapore General Hospital, National Neuroscience Institute, Singapore – sequence: 11 givenname: Z.J. surname: Zhang fullname: Zhang, Z.J. organization: Department of Neurology, West China Hospital, Sichuan University, Chengdu, China – sequence: 12 givenname: X.K. surname: An fullname: An, X.K. organization: Department of Neurology, West China Hospital, Sichuan University, Chengdu, China – sequence: 13 givenname: G.J. surname: Lee-Chen fullname: Lee-Chen, G.J. organization: Department of Life Science, National Taiwan Normal University, Taipei, Taiwan – sequence: 14 givenname: M.C. surname: Lee fullname: Lee, M.C. organization: Department of Neurology, Cathay General Hospital, Taipei, Taiwan – sequence: 15 givenname: S. surname: Fook-Chong fullname: Fook-Chong, S. organization: Departments of Neurology and Clinical Research, Singapore General Hospital, National Neuroscience Institute, Singapore – sequence: 16 givenname: J.M. surname: Burgunder fullname: Burgunder, J.M. organization: Department of Neurology, University of Bern, Bern, Switzerland – sequence: 17 givenname: R.M. surname: Wu fullname: Wu, R.M. organization: Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan – sequence: 18 givenname: Y.R. surname: Wu fullname: Wu, Y.R. email: yihruwu@adm.cgmh.org.tw organization: Department of Neurology, Chang Gung Memorial Hospital and College of Medicine, Chang Gung University, Taipei, Taiwan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19329225$$D View this record in MEDLINE/PubMed |
BookMark | eNqNktFrFDEQxoNU7LX6L0gehD7tNpPdbDYgQj1tqxwoaJ9DLjt7zXUvaZPdwv335rgqWBAPAvPyzS_fzDcn5MgHj4S8A1YCg-Z8XXqcYli6MJiV86uSM9aWAGUuL8gMhGgLqJU8IjMGSha1aNkxOUlpzRiTtWxekWNQFVecixn5euHNsE0u0dDT8Rbpzfx6AXSFHkdn6aOJzviROk-_m3jnfAr-LNHOJTQJqdkEv6LzW-cx4WvysjdDwjdP9ZTcXH7-Ob8uFt-uvswvFoVtRDUWHQPeV2120qLNBpfCoq1E04jetp3lgnME2VlgVb-0EkylZFVDW9cKDe9FdUrO9tz7GB4mTKPeuGRxGIzHMCXdKgWVzLP_VymFaqUCxbPy7ZNyWm6w0_fRbUzc6t-LyoKPe4GNIaWIvbZuNKMLfozGDRqY3qWj1_rvdPQuHQ2gc8mQ988gf_45rP1y3455u48Oo07WobfYuYh21F1wh4I-PAPZwXlnzXCHW0zrMMV8FUmDTlwz_WN3R7szYvnVrIYM-PRvwOE-fgE5geBQ |
CitedBy_id | crossref_primary_10_1016_j_gene_2012_11_003 crossref_primary_10_1007_s11356_021_14619_6 crossref_primary_10_1016_j_parkreldis_2011_01_019 crossref_primary_10_1159_000367995 crossref_primary_10_1186_1471_2377_12_62 crossref_primary_10_1186_1756_9966_30_79 crossref_primary_10_3390_ijms25021303 crossref_primary_10_1007_s10072_014_1973_4 crossref_primary_10_2174_1871527319666200905115548 crossref_primary_10_5607_en_2015_24_2_103 |
Cites_doi | 10.1111/j.1468-1331.2007.02012.x 10.1002/ana.20757 10.1002/ana.20017 10.1002/mds.21064 10.1016/j.neulet.2008.07.012 10.1016/S0092-8674(02)01012-7 10.1002/mds.10326 |
ContentType | Journal Article |
Copyright | 2008 Elsevier Inc. Elsevier Inc. Copyright © 2008 Elsevier Inc. All rights reserved. |
Copyright_xml | – notice: 2008 Elsevier Inc. – notice: Elsevier Inc. – notice: Copyright © 2008 Elsevier Inc. All rights reserved. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 7TK 8FD FR3 P64 RC3 |
DOI | 10.1016/j.neurobiolaging.2008.11.008 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic Neurosciences Abstracts Technology Research Database Engineering Research Database Biotechnology and BioEngineering Abstracts Genetics Abstracts |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic Genetics Abstracts Engineering Research Database Technology Research Database Neurosciences Abstracts Biotechnology and BioEngineering Abstracts |
DatabaseTitleList | Genetics Abstracts MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
EISSN | 1558-1497 |
EndPage | 2196 |
ExternalDocumentID | 19329225 10_1016_j_neurobiolaging_2008_11_008 S0197458008004041 1_s2_0_S0197458008004041 |
Genre | Research Support, Non-U.S. Gov't Multicenter Study Journal Article |
GeographicLocations | Singapore Taiwan |
GeographicLocations_xml | – name: Singapore – name: Taiwan |
GroupedDBID | --- --K --M -~X .1- .FO .GJ .~1 0R~ 123 1B1 1P~ 1RT 1~. 1~5 29N 4.4 457 4G. 53G 5RE 5VS 7-5 71M 8P~ 9JM 9JO AABNK AADFP AAEDT AAEDW AAGJA AAGUQ AAIKJ AAKOC AALRI AAOAW AAQFI AAQXK AATTM AAXKI AAXLA AAXUO AAYWO ABBQC ABCQJ ABFNM ABFRF ABGSF ABIVO ABJNI ABLJU ABMAC ABMZM ABOYX ABUDA ABWVN ABXDB ACDAQ ACGFO ACGFS ACIEU ACIUM ACRLP ACRPL ACVFH ACXNI ADBBV ADCNI ADEZE ADMUD ADNMO ADUVX AEBSH AEFWE AEHWI AEIPS AEKER AENEX AEUPX AEVXI AFJKZ AFPUW AFRHN AFTJW AFXIZ AGCQF AGHFR AGQPQ AGRDE AGUBO AGWIK AGYEJ AHHHB AIEXJ AIGII AIIUN AIKHN AITUG AJRQY AJUYK AKBMS AKRLJ AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ANZVX APXCP ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC BNPGV CS3 DU5 EBS EFJIC EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-2 G-Q GBLVA HDW HMK HMO HMQ HVGLF HZ~ IHE J1W KOM LX8 M29 M2V M41 MO0 MOBAO MVM N9A O-L O9- OAUVE OD~ OKEIE OO0 OZT P-8 P-9 P2P PC. Q38 R2- ROL RPZ SAE SCC SDF SDG SDP SEL SES SEW SNS SPCBC SSB SSH SSN SSU SSY SSZ T5K WUQ Z5R ZGI ~G- AACTN AFCTW AFKWA AJOXV AMFUW RIG AADPK AAIAV ABLVK ABYKQ AFYLN AJBFU DOVZS EFLBG LCYCR AAYXX AGRNS CITATION CGR CUY CVF ECM EIF NPM 7X8 7TK 8FD FR3 P64 RC3 |
ID | FETCH-LOGICAL-c653t-d012f387478ec197b5cec35665fc8dc2522e17dc103fbc71a3973418449ea2f53 |
IEDL.DBID | AIKHN |
ISSN | 0197-4580 1558-1497 |
IngestDate | Mon Jul 21 11:14:33 EDT 2025 Mon Jul 21 10:51:48 EDT 2025 Mon Jul 21 05:44:49 EDT 2025 Tue Jul 01 01:27:59 EDT 2025 Thu Apr 24 22:56:43 EDT 2025 Fri Feb 23 02:27:30 EST 2024 Sun Feb 23 10:19:35 EST 2025 Tue Aug 26 16:32:23 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 12 |
Keywords | UCHL1 Parkinson's disease Polymorphism |
Language | English |
License | https://www.elsevier.com/tdm/userlicense/1.0 Copyright © 2008 Elsevier Inc. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c653t-d012f387478ec197b5cec35665fc8dc2522e17dc103fbc71a3973418449ea2f53 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
OpenAccessLink | http://scholarbank.nus.edu.sg/handle/10635/109930 |
PMID | 19329225 |
PQID | 759879192 |
PQPubID | 23479 |
PageCount | 3 |
ParticipantIDs | proquest_miscellaneous_899137019 proquest_miscellaneous_759879192 pubmed_primary_19329225 crossref_citationtrail_10_1016_j_neurobiolaging_2008_11_008 crossref_primary_10_1016_j_neurobiolaging_2008_11_008 elsevier_sciencedirect_doi_10_1016_j_neurobiolaging_2008_11_008 elsevier_clinicalkeyesjournals_1_s2_0_S0197458008004041 elsevier_clinicalkey_doi_10_1016_j_neurobiolaging_2008_11_008 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2010-12-01 |
PublicationDateYYYYMMDD | 2010-12-01 |
PublicationDate_xml | – month: 12 year: 2010 text: 2010-12-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Neurobiology of aging |
PublicationTitleAlternate | Neurobiol Aging |
PublicationYear | 2010 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
References | Zhang, Burgunder, An, Wu, Chen, Zhang, Wang, Xu, Gou, Yuan, Mao, Peng (bib7) 2008; 442 Hutter, Samii, Factor, Nutt, Higgins, Bird, Griffith, Roberts, Leis, Montimurro, Kay, Edwards, Payami, Zabetian (bib3) 2008; 15 Healy, Abou-Sleiman, Casas, Ahmadi, Lynch, Gandhi, Muqit, Foltynie, Barker, Bhatia, Quinn, Lees, Gibson, Holton, Revesz, Goldstein, Wood (bib2) 2006; 59 Maraganore, Lesnick, Elbaz (bib5) 2004; 55 Elbaz, Levecque, Clavel, SVidal, Richard, Corrèze, Delemotte, Amouyel, Alpérovitch, Chartier-Harlin, Tzourio (bib1) 2003; 18 Liu, Fallon, Lashuel, Liu, Lansbury (bib4) 2002; 111 Tan, Puong, Fook-Chong, Chua, Shen, Yuen, Pavanni, Wong, Puvan, Zhao (bib6) 2006; 21 Healy (10.1016/j.neurobiolaging.2008.11.008_bib2) 2006; 59 Tan (10.1016/j.neurobiolaging.2008.11.008_bib6) 2006; 21 Elbaz (10.1016/j.neurobiolaging.2008.11.008_bib1) 2003; 18 Zhang (10.1016/j.neurobiolaging.2008.11.008_bib7) 2008; 442 Maraganore (10.1016/j.neurobiolaging.2008.11.008_bib5) 2004; 55 Liu (10.1016/j.neurobiolaging.2008.11.008_bib4) 2002; 111 Hutter (10.1016/j.neurobiolaging.2008.11.008_bib3) 2008; 15 |
References_xml | – volume: 55 start-page: 512 year: 2004 end-page: 521 ident: bib5 article-title: UCHL1 is a Parkinson's disease susceptibility gene publication-title: Ann. Neurol. – volume: 442 start-page: 200 year: 2008 end-page: 202 ident: bib7 article-title: Lack of evidence for association of a UCHL1 S18Y polymorphism with Parkinson's disease in a Han Chinese population publication-title: Neurosci. Lett. – volume: 111 start-page: 209 year: 2002 end-page: 218 ident: bib4 article-title: The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha synuclein degradation and Parkinson's disease susceptibility publication-title: Cell – volume: 59 start-page: 627 year: 2006 end-page: 633 ident: bib2 article-title: UCHL-1 is not a Parkinson's disease susceptibility gene publication-title: Ann. Neurol. – volume: 21 start-page: 1765 year: 2006 end-page: 1768 ident: bib6 article-title: Case-control study of UCHL1 S18Y variant in Parkinson's disease publication-title: Mov. Disord. – volume: 15 start-page: 134 year: 2008 end-page: 139 ident: bib3 article-title: Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease publication-title: Eur. J. Neurol. – volume: 18 start-page: 130 year: 2003 end-page: 137 ident: bib1 article-title: 18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship publication-title: Mov. Disord. – volume: 15 start-page: 134 issue: 2 year: 2008 ident: 10.1016/j.neurobiolaging.2008.11.008_bib3 article-title: Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease publication-title: Eur. J. Neurol. doi: 10.1111/j.1468-1331.2007.02012.x – volume: 59 start-page: 627 issue: 4 year: 2006 ident: 10.1016/j.neurobiolaging.2008.11.008_bib2 article-title: UCHL-1 is not a Parkinson's disease susceptibility gene publication-title: Ann. Neurol. doi: 10.1002/ana.20757 – volume: 55 start-page: 512 year: 2004 ident: 10.1016/j.neurobiolaging.2008.11.008_bib5 article-title: UCHL1 is a Parkinson's disease susceptibility gene publication-title: Ann. Neurol. doi: 10.1002/ana.20017 – volume: 21 start-page: 1765 issue: 10 year: 2006 ident: 10.1016/j.neurobiolaging.2008.11.008_bib6 article-title: Case-control study of UCHL1 S18Y variant in Parkinson's disease publication-title: Mov. Disord. doi: 10.1002/mds.21064 – volume: 442 start-page: 200 issue: 3 year: 2008 ident: 10.1016/j.neurobiolaging.2008.11.008_bib7 article-title: Lack of evidence for association of a UCHL1 S18Y polymorphism with Parkinson's disease in a Han Chinese population publication-title: Neurosci. Lett. doi: 10.1016/j.neulet.2008.07.012 – volume: 111 start-page: 209 issue: 2 year: 2002 ident: 10.1016/j.neurobiolaging.2008.11.008_bib4 article-title: The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha synuclein degradation and Parkinson's disease susceptibility publication-title: Cell doi: 10.1016/S0092-8674(02)01012-7 – volume: 18 start-page: 130 issue: 2 year: 2003 ident: 10.1016/j.neurobiolaging.2008.11.008_bib1 article-title: 18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship publication-title: Mov. Disord. doi: 10.1002/mds.10326 |
SSID | ssj0007476 |
Score | 2.0621483 |
Snippet | The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (
UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian... Abstract The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 ( UCHL1 ) S18Y variant with Parkinson's disease (PD) among Caucasian... The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian... |
SourceID | proquest pubmed crossref elsevier |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 2194 |
SubjectTerms | Adolescent Adult Age of Onset Aged Aged, 80 and over Asian Continental Ancestry Group - ethnology Asian Continental Ancestry Group - genetics Female Genetic Association Studies Genetic Variation - genetics Humans Internal Medicine Male Middle Aged Neurology Parkinson Disease - enzymology Parkinson Disease - epidemiology Parkinson Disease - genetics Parkinson's disease Polymorphism Singapore - epidemiology Singapore - ethnology Taiwan - epidemiology Taiwan - ethnology Ubiquitin Thiolesterase - genetics Ubiquitination - genetics UCHL1 Young Adult |
Title | Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0197458008004041 https://www.clinicalkey.es/playcontent/1-s2.0-S0197458008004041 https://dx.doi.org/10.1016/j.neurobiolaging.2008.11.008 https://www.ncbi.nlm.nih.gov/pubmed/19329225 https://www.proquest.com/docview/759879192 https://www.proquest.com/docview/899137019 |
Volume | 31 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEB58gHgR39YXexA9xSbZvBYRKUWp9XHRgrcl2exCRdNiWsGLv93ZzaYiVlA8BUKGLJPZmW-yM98AHDCWidRVzJFpSB30frHDEpY7LFY5GojAIKR_DdzcRp1e0H0IH2agXffC6LJK6_srn268tb3TtNpsDvv95h2CkzgIE4N5Alc3r8_7lEVo2vOty6vO7cQhI2KOqq5pTfGduAtw8FnmZWgjNeGRGQpUFVdqWk89b3J6pPoJiZqIdLEMSxZKkla12hWYkcUqrLUKTKOf38ghMcWd5q_5GnRr8hEyUAQxH-m1O9ceQevRTYzkFTNmVDHpF0S3QZuOsKOS2NMbYiYSET1qW5ZyHXoX5_ftjmPHKDgiCunIyTEGKZpoonwpUAdZKKSgCON0-VYufERg0otz4blUZSL2UoQoGNuSIGAy9VVIN2CuGBRyCwhLlZdkUkY5RSSTBZkfZGkaqVzp01UqG3BSq4wLyzGuR1088bqY7JF_VXg1BhOTELw0IJxIDyuujV_KndZfh9f9pOgBOQaFX8rH0-RlabdzyT1e-tzl30yuAWcTyS9W-4d3k9qcOG5sfVqTFnIwLnkcsiRmCMB_fgRzZY9qPv0GbFaW-Kk3xOUMffX2v1e4A4v-pIRnF-ZGL2O5h0BslO3D7PG7t2-32wfOCjSP |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3di9NAEB-OEzxfRO2d5vzah6JPuSbZfC0iUoql1vZevELflmSzCz00LZdW8MW_3ZlN0lK8QsWnQMiQZTIfv83O_AagK0SuMs8IV2cRdzH6Ja5IReGKxBRoIAqTEP0amF7Ho1k4nkfzExi0vTBUVtnE_jqm22jd3Ok12uytFoveNwQnSRilFvOEHjWvPwjRfck7r37v6jwQL8d1zzQRfKfeQ-juirwsaSTRHdmRQHVpJZF60rTJ-_PUIRxq89HwCTxugCTr12t9Cie6fAadfomb6B-_2DtmSzvtP_MOjFvqEbY0DBEfmw1GE5-h7VALI_uJ-2VUMFuUjJqgbT_Y-4o1ZzfMziNiNGhbV_ocZsPPN4OR2wxRcFUc8bVbYAYyPCWafK1QB3mktOII4qh4q1AB4i_tJ4XyPW5ylfgZAhTMbGkYCp0FJuIXcFouS_0CmMiMn-ZaxwVHHJOHeRDmWRabwtDZKtcOfGhVJlXDME6DLr7LtpTsVu4rvB6CiVsQvDgQbaVXNdPGkXIf268j225SjH8SU8KR8sl98rpqnLmSvqwC6cm_DM6BT1vJPZv9h3ez1pwkujWd1WSlXm4qmUQiTQTC78OP4E7Z58Sm78Dz2hJ3ekNULjBSX_73Ct_C2ehmOpGTL9dfX8KjYFvM8wpO13cb_Roh2Tp_Y13uD176NVM |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Analysis+of+the+UCHL1+genetic+variant+in+Parkinson%27s+disease+among+Chinese&rft.jtitle=Neurobiology+of+aging&rft.au=Tan%2C+E+K&rft.au=Lu%2C+C+S&rft.au=Peng%2C+R&rft.au=Teo%2C+Y+Y&rft.date=2010-12-01&rft.issn=0197-4580&rft.volume=31&rft.issue=12&rft.spage=2194&rft.epage=2196&rft_id=info:doi/10.1016%2Fj.neurobiolaging.2008.11.008&rft.externalDBID=NO_FULL_TEXT |
thumbnail_m | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F01974580%2FS0197458010X00100%2Fcov150h.gif |