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Tag lrrk2 [12 articles]

Recent papers classified by the tag lrrk2.
  • A common LRRK2 mutation in idiopathic Parkinson's disease
    The Lancet, Vol. 365, No. 9457. (29 January 2005), pp. 415-416.
    by William P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, Shushant Jain, Andrew Singleton, Andrew J Lees, Karen Shaw, Kailash P Bhatia, Vincenzo Bonifati, Niall P Quinn, John Lynch, Daniel G Healy, Janice L Holton, Tamas Revesz, Nicholas W Wood
    posted to pd genetics lrrk2 by psique on 2008-04-29 17:24:43 as ** along with 1 group parkinson's disease references
  • Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
    Brain : a journal of neurology, Vol. 128, No. Pt 12. (December 2005), pp. 2786-2796.
    by NL Khan, S Jain, JM Lynch, N Pavese, P Abou-Sleiman, JL Holton, DG Healy, WP Gilks, MG Sweeney, M Ganguly, V Gibbons, S Gandhi, J Vaughan, LH Eunson, R Katzenschlager, J Gayton, G Lennox, T Revesz, D Nicholl, KP Bhatia, N Quinn, D Brooks, AJ Lees, MB Davis, P Piccini, AB Singleton, NW Wood
    posted to pd genetics lrrk2 by psique on 2008-04-29 17:03:53 as ** along with 1 group parkinson's disease references
  • Impact of recent genetic findings in Parkinson's disease.
    Current opinion in neurology, Vol. 20, No. 4. (August 2007), pp. 453-464.
  • The Chaperone Activity of Heat Shock Protein 90 Is Critical for Maintaining the Stability of Leucine-Rich Repeat Kinase 2
    J. Neurosci., Vol. 28, No. 13. (26 March 2008), pp. 3384-3391.
    by Lizhen Wang, Chengsong Xie, Elisa Greggio, Loukia Parisiadou, Hoon Shim, Lixin Sun, Jayanth Chandran, Xian Lin, Chen Lai, Wan-Jou Yang, Darren J Moore, Ted M Dawson, Valina L Dawson, Gabriela Chiosis, Mark R Cookson, Huaibin Cai
  • LRRK2 mutations in Basque patients with Parkinson's disease - Authors' reply
    The Lancet Neurology, Vol. 7, No. 10. (October 2008), pp. 867-867.
    by Daniel G Healy
    posted to pd lrrk2 genetics by psique on 2008-09-17 15:03:53 as read along with 1 group parkinson's disease references
  • Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2
    BMC Neurology, Vol. 8 (22 January 2008), 1.
    by Jose Bras, Rita Guerreiro, Maria Ribeiro, Ana Morgadinho, Cristina Januario, Margarida Dias, Ana Calado, Cristina Semedo, Catarina Oliveira, John Hardy, Andrew Singleton
  • Distribution of PINK1 and LRRK2 in rat and mouse brain
    Journal of Neurochemistry, Vol. 98, No. 3. (August 2006), pp. 951-961.
    posted to pink1 pd lrrk2 by psique on 2008-09-18 13:23:16 as *** along with 1 group parkinson's disease references
  • Mutations in LRRK2 as a cause of Parkinson's disease.
    Neuro-Signals, Vol. 16, No. 1. (2008), pp. 99-105.
    posted to pd lrrk2 by psique on 2008-06-12 19:12:18 as ** along with 1 group parkinson's disease references
  • LRRK2 mutations in Basque patients with Parkinson's disease
    The Lancet Neurology, Vol. 7, No. 10. (October 2008), pp. 866-867.
    by Juan J Zarranz, Juan C Gómez-Esteban
    posted to pd lrrk2 genetics by psique on 2008-09-17 14:59:44 as read along with 1 group parkinson's disease references
  • Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity.
    Proc Natl Acad Sci U S A, Vol. 102, No. 46. (15 November 2005), pp. 16842-16847.
    by AB West, DJ Moore, S Biskup, A Bugayenko, WW Smith, CA Ross, VL Dawson, TM Dawson
    posted to lrrk2 mitochondrial parkinson by novrain on 2007-06-25 03:57:15 as ***
  • Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.
    J Neurol Sci (18 March 2008)
    by Carles Gaig, Mario Ezquerra, Maria José J Martí, Francesc Valldeoriola, Esteban Muñoz, Albert Lladó, Maria Jesús J Rey, Adriana Cardozo, José Luis L Molinuevo, Eduardo Tolosa
    posted to ftd lrrk2 by giovanni on 2008-03-21 20:54:18 as **
  • Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations
    Neurology, Vol. 70, No. 7. (12 February 2008), pp. 521-527.
    by AS Chen-Plotkin, W Yuan, C Anderson, Mccarty E Wood, HI Hurtig, CM Clark, BL Miller, Lee, JQ Trojanowski, M Grossman, Van VM Deerlin
    posted to cbd lrrk2 ppa by applebyb on 2008-02-11 22:07:51 as ****
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