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There are 13306 results for: content related to: Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients

  1. Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinoma

    Genes, Chromosomes and Cancer

    Volume 51, Issue 5, May 2012, Pages: 462–472, Reika Iwakawa, Hirokazu Okayama, Takashi Kohno, Aiko Sato-Otsubo, Seishi Ogawa and Jun Yokota

    Version of Record online : 3 FEB 2012, DOI: 10.1002/gcc.21933

  2. Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease

    Movement Disorders

    Volume 27, Issue 12, October 2012, Pages: 1522–1529, Laura L. Kilarski, Justin P. Pearson, Victoria Newsway, Elisa Majounie, M. Duleeka W. Knipe, Anjum Misbahuddin, Patrick F. Chinnery, David J. Burn, Carl E. Clarke, Marie-Helene Marion, Alistair J. Lewthwaite, David J. Nicholl, Nicholas W. Wood, Karen E. Morrison, Caroline H. Williams-Gray, Jonathan R. Evans, Stephen J. Sawcer, Roger A. Barker, Mirdhu M. Wickremaratchi, Yoav Ben-Shlomo, Nigel M. Williams and Huw R. Morris

    Version of Record online : 6 SEP 2012, DOI: 10.1002/mds.25132

  3. PARK2 and PACRG are commonly downregulated in clear-cell renal cell carcinoma and are associated with aggressive disease and poor clinical outcome

    Genes, Chromosomes and Cancer

    Volume 52, Issue 3, March 2013, Pages: 265–273, Marieta I. Toma, Daniela Wuttig, Sandy Kaiser, Alexander Herr, Thomas Weber, Stefan Zastrow, Rainer Koch, Matthias Meinhardt, Gustavo B. Baretton, Manfred P. Wirth and Susanne Fuessel

    Version of Record online : 2 NOV 2012, DOI: 10.1002/gcc.22026

  4. Genetic mutations in early-onset Parkinson's disease Mexican patients: Molecular testing implications

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 3, April 2014, Pages: 235–244, Nancy Monroy-Jaramillo, Jorge Luis Guerrero-Camacho, Mayela Rodríguez-Violante, Marie-Catherine Boll-Woehrlen, Petra Yescas-Gómez, María Elisa Alonso-Vilatela and Marisol López-López

    Version of Record online : 23 FEB 2014, DOI: 10.1002/ajmg.b.32228

  5. Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer

    Genes, Chromosomes and Cancer

    Volume 38, Issue 1, September 2003, Pages: 40–52, Stacy R. Denison, Gwen Callahan, Nicole A. Becker, Leslie A. Phillips and David I. Smith

    Version of Record online : 16 JUN 2003, DOI: 10.1002/gcc.10236

  6. You have free access to this content
    Effective Variant Detection by Targeted Deep Sequencing of DNA Pools: An Example from Parkinson's Disease

    Annals of Human Genetics

    Volume 78, Issue 3, May 2014, Pages: 243–252, Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå and Mathias Toft

    Version of Record online : 24 MAR 2014, DOI: 10.1111/ahg.12060

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    LRRK2 in Parkinson’s disease: in vivo models and approaches for understanding pathogenic roles

    The FEBS Journal

    Volume 276, Issue 22, November 2009, Pages: 6445–6454, Zhenyu Yue

    Version of Record online : 5 OCT 2009, DOI: 10.1111/j.1742-4658.2009.07343.x

  8. You have free access to this content
    PARK2/PACRG polymorphisms and susceptibility to typhoid and paratyphoid fever

    Clinical & Experimental Immunology

    Volume 144, Issue 3, June 2006, Pages: 425–431, S. Ali, A. M. Vollaard, S. Widjaja, C. Surjadi, E. Van De Vosse and J. T. Van Dissel

    Version of Record online : 21 APR 2006, DOI: 10.1111/j.1365-2249.2006.03087.x

  9. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  10. Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease

    Clinical Genetics

    Volume 82, Issue 1, July 2012, Pages: 77–82, S Y Kim, M W Seong, B S Jeon, S Y Kim, H S Ko, J Y Kim and S S Park

    Version of Record online : 29 MAY 2011, DOI: 10.1111/j.1399-0004.2011.01693.x

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    A single-nucleotide mutation in the −10 promoter region inactivates the narK2X promoter in Mycobacterium bovis and Mycobacterium bovis BCG and has an application in diagnosis

    FEMS Microbiology Letters

    Volume 303, Issue 2, February 2010, Pages: 190–196, Santosh Chauhan, Alka Singh and Jaya Sivaswami Tyagi

    Version of Record online : 3 DEC 2009, DOI: 10.1111/j.1574-6968.2009.01876.x

  12. Genome-wide identification, annotation and expression profile analysis of SnRK2 gene family in grapevine

    Australian Journal of Grape and Wine Research

    Volume 22, Issue 3, October 2016, Pages: 478–488, J.-Y. Liu, N.-N. Chen, Z.-M. Cheng and J.-S. Xiong

    Version of Record online : 20 JUN 2016, DOI: 10.1111/ajgw.12223

  13. Using biological knowledge to discover higher order interactions in genetic association studies

    Genetic Epidemiology

    Volume 34, Issue 8, December 2010, Pages: 863–878, Gary K. Chen and Duncan C Thomas

    Version of Record online : 22 NOV 2010, DOI: 10.1002/gepi.20542

  14. Molecular imaging in hereditary forms of parkinsonism

    European Journal of Neurology

    Volume 14, Issue 4, April 2007, Pages: 359–368, M. C. Shih, A. C. Felicio, C. De Oliveira Godeiro-Junior, P. De Carvalho Aguiar, L. A. F. De Andrade, H. B. Ferraz and R. A. Bressan

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1468-1331.2007.01691.x

  15. The curious case of phenocopies in families with genetic Parkinson's disease

    Movement Disorders

    Volume 26, Issue 10, 15 August 2011, Pages: 1793–1802, Christine Klein, Rosalind Chuang, Connie Marras and Anthony E. Lang

    Version of Record online : 6 JUL 2011, DOI: 10.1002/mds.23853

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    Genetic risk factors for cognitive decline in Parkinson's disease: a review of the literature

    European Journal of Neurology

    E. S. Fagan and L. Pihlstrøm

    Version of Record online : 21 FEB 2017, DOI: 10.1111/ene.13258

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    ERK1 and ERK2 are required for radial glial maintenance and cortical lamination

    Genes to Cells

    Volume 15, Issue 10, October 2010, Pages: 1072–1088, Osamu Imamura, Gilles Pagès, Jacques Pouysségur, Shogo Endo and Kunio Takishima

    Version of Record online : 5 SEP 2010, DOI: 10.1111/j.1365-2443.2010.01444.x

  18. High-Resolution Survey in Familial Parkinson Disease Genes Reveals Multiple Independent Copy Number Variation Events in PARK2

    Human Mutation

    Volume 34, Issue 8, August 2013, Pages: 1071–1074, Liyong Wang, Karen Nuytemans, Guney Bademci, Cherylyn Jauregui, Eden R. Martin, William K. Scott, Jeffery M. Vance and Stephan Zuchner

    Version of Record online : 28 MAY 2013, DOI: 10.1002/humu.22344

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    Modeling human neurological disorders with induced pluripotent stem cells

    Journal of Neurochemistry

    Volume 129, Issue 3, May 2014, Pages: 388–399, Yoichi Imaizumi and Hideyuki Okano

    Version of Record online : 15 DEC 2013, DOI: 10.1111/jnc.12625

  20. Defining neurodegeneration on Guam by targeted genomic sequencing

    Annals of Neurology

    Volume 77, Issue 3, March 2015, Pages: 458–468, John C. Steele, Ilaria Guella, Chelsea Szu-Tu, Michelle K. Lin, Christina Thompson, Daniel M. Evans, Holly E. Sherman, Carles Vilariño-Güell, Katrina Gwinn, Huw Morris, Dennis W. Dickson and Matthew J. Farrer

    Version of Record online : 3 FEB 2015, DOI: 10.1002/ana.24346