Author Ruiz-Martínez, Javier
Infante, Jon
Gorostidi, Ana
González-Aramburu, Isabel
Martí-Massó, José Félix
Combarros, Onofre
Sierra, María
Berciano, José
Sánchez-Juan, Pascual
García-Gorostiaga, Inés
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10.1074/jbc.M600933200
10.1016/S0140-6736(10)62345-8
10.1002/ajmg.b.31129
10.1523/JNEUROSCI.0341-06.2006
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References Arawaka, Wada, Goto, Karube, Sakamoto, Ren (bib2) 2006; 26
Anderson, Walker, Goldstein, de Laat, Banducci, Caccavello (bib1) 2006; 281
(bib5) 2011; 377
Ryu, Kim, Arima, Mouradian, Kim, Lee (bib3) 2008; 266
Tarantino, de Marco, Annesi, Rocca, Annesi, Civitelli (bib4) 2011; 156
Arawaka (10.1016/j.parkreldis.2011.04.003_bib2) 2006; 26
(10.1016/j.parkreldis.2011.04.003_bib5) 2011; 377
Anderson (10.1016/j.parkreldis.2011.04.003_bib1) 2006; 281
Ryu (10.1016/j.parkreldis.2011.04.003_bib3) 2008; 266
Tarantino (10.1016/j.parkreldis.2011.04.003_bib4) 2011; 156
References_xml – volume: 281
  start-page: 29739
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  ident: bib1
  article-title: Phosphorylation of Ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body disease
  publication-title: J Biol Chem
  contributor:
    fullname: Caccavello
– volume: 377
  start-page: 641
  year: 2011
  end-page: 649
  ident: bib5
  article-title: Imputation of sequence variants for identification of genetic risks for Parkinson’s disease: a meta-analysis of genome-wide association studies
  publication-title: Lancet
– volume: 26
  start-page: 9227
  year: 2006
  end-page: 9238
  ident: bib2
  article-title: The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson’s disease
  publication-title: J Neurosci
  contributor:
    fullname: Ren
– volume: 156
  start-page: 104
  year: 2011
  end-page: 107
  ident: bib4
  article-title: Lack of association between G-Protein coupled receptor kinase 5 gene and Parkinson’s disease
  publication-title: Am J Med Genet Part B
  contributor:
    fullname: Civitelli
– volume: 266
  start-page: 9
  year: 2008
  end-page: 12
  ident: bib3
  article-title: Localization of CKII beta subunits in Lewy bodies of Parkinson’s disease
  publication-title: J Neurol Sci
  contributor:
    fullname: Lee
– volume: 266
  start-page: 9
  issue: 1–2
  year: 2008
  ident: 10.1016/j.parkreldis.2011.04.003_bib3
  article-title: Localization of CKII beta subunits in Lewy bodies of Parkinson’s disease
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2007.08.027
  contributor:
    fullname: Ryu
– volume: 281
  start-page: 29739
  issue: 40
  year: 2006
  ident: 10.1016/j.parkreldis.2011.04.003_bib1
  article-title: Phosphorylation of Ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body disease
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M600933200
  contributor:
    fullname: Anderson
– volume: 377
  start-page: 641
  year: 2011
  ident: 10.1016/j.parkreldis.2011.04.003_bib5
  article-title: Imputation of sequence variants for identification of genetic risks for Parkinson’s disease: a meta-analysis of genome-wide association studies
  publication-title: Lancet
  doi: 10.1016/S0140-6736(10)62345-8
– volume: 156
  start-page: 104
  issue: 1
  year: 2011
  ident: 10.1016/j.parkreldis.2011.04.003_bib4
  article-title: Lack of association between G-Protein coupled receptor kinase 5 gene and Parkinson’s disease
  publication-title: Am J Med Genet Part B
  doi: 10.1002/ajmg.b.31129
  contributor:
    fullname: Tarantino
– volume: 26
  start-page: 9227
  issue: 36
  year: 2006
  ident: 10.1016/j.parkreldis.2011.04.003_bib2
  article-title: The role of G-protein-coupled receptor kinase 5 in pathogenesis of sporadic Parkinson’s disease
  publication-title: J Neurosci
  doi: 10.1523/JNEUROSCI.0341-06.2006
  contributor:
    fullname: Arawaka
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SubjectTerms Aged
Case-Control Studies
Casein Kinase II - genetics
Female
Genetic Predisposition to Disease
Genotype
Humans
Indexing in process
Male
Middle Aged
Neurology
Parkinson Disease - genetics
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Receptors, G-Protein-Coupled - genetics
Risk Factors
Spain
Title Genetic variation in α-synuclein kinases (CK-2β and GRK-5) and risk of Parkinson’s disease
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