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Identification of potential protein interactors of Lrrk2.

Identification of potential protein interactors of Lrrk2. Research Abstract Details 

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  • Identification of potential protein interactors of Lrrk2. Abstract Text:

    justus c Justus C ,julie p taylorJulie P Taylor,su san mokSu San Mok,owen a rossOwen A Ross,kelly m hinkleKelly M Hinkle,rachel m baileyRachel M Bailey,jacob h hinesJacob H Hines,jennifer szutuJennifer Szutu,benjamin maddenBenjamin Madden,leonard petrucelliLeonard Petrucelli,matthew j farrerMatthew J Farrer,justus c Justus C ,julie p taylorJulie P Taylor,su san mokSu San Mok,owen a rossOwen A Ross,kelly m hinkleKelly M Hinkle,rachel m baileyRachel M Bailey,jacob h hinesJacob H Hines,jennifer szutuJennifer Szutu,benjamin maddenBenjamin Madden,leonard petrucelliLeonard Petrucelli,matthew j farrerMatthew J Farrer,

    Pathogenic substitutions in the Lrrk2 protein have been shown to be an important cause of both familial and sporadic parkinsonism. The molecular pathway involved in Lrrk2 dopaminergic neuron degeneration remains elusive. Employing a combination of Lrrk2-mediated protein precipitation and tandem mass spectrometry, we identified 14 potential Lrrk2 binding partners. The majority of these interactions may be subgrouped into three functional cellular pathways: (i) chaperone-mediated response, (ii) proteins associated with the cytoskeleton and trafficking and (iii) phosphorylation and kinase activity. Future investigation of these candidates is now warranted and may help resolve the pathomechanism behind Lrrk2 neurodegeneration.

    Identification of potential protein interactors of Lrrk2. Publishing Authors By Initials

    jc JC ,jp taylorJP Taylor,ss mokSS Mok,oa rossOA Ross,km hinkleKM Hinkle,rm baileyRM Bailey,jh hinesJH Hines,j szutuJ Szutu,b maddenB Madden,l petrucelliL Petrucelli,mj farrerMJ Farrer,jc JC ,jp taylorJP Taylor,ss mokSS Mok,oa rossOA Ross,km hinkleKM Hinkle,rm baileyRM Bailey,jh hinesJH Hines,j szutuJ Szutu,b maddenB Madden,l petrucelliL Petrucelli,mj farrerMJ Farrer,

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    PUBMED ID PMID:

    MEDLINE DATE:

    Identification of potential protein interactors of Lrrk2. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Parkinsonism & related disorders

    VOLUME: 13

    Page Numbers: 382-5

    Journal Abbreviation: Parkinsonism Relat. Disord.

    ISSN: 1353-8020

    DAY: 2

    MONTH: 04

    YEAR: 2007

    Identification of potential protein interactors of Lrrk2. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9513583

    Identification of potential protein interactors of Lrrk2. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Identification of potential protein interactors of Lrrk2. Information

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    Grant and Affiliation Information for Identification of potential protein interactors of Lrrk2.

    AFFILIATION: Department of Neuroscience and Neurology, Mayo Clinic College of Medicine, Birdsall Building, Jacksonville, FL 32224, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NINDS

    GRANT: P50 NS40256

    ACRONYM: NS

    MEDLINETA: Parkinsonism Relat Disord

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