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  1. 1
    DJ-1 Transcriptionally Up-regulates the Human Tyrosine Hydroxylase by Inhibiting the Sumoylation of Pyrimidine Tract-binding Protein-associated Splicing Factor

    DJ-1 Transcriptionally Up-regulates the Human Tyrosine Hydroxylase by Inhibiting the Sumoylation of Pyrimidine Tract-binding Protein-associated Splicing Factor por Nan Zhong, Christina Y. Kim, Patrizia Rizzu, Changiz Geula, Douglas R. Porter, Emmanuel N. Pothos, Ferdinando Squitieri, Peter Heutink, Jin Xu

    Publicado em 2006
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  2. 2
    Drosophila DJ-1 Mutants Are Selectively Sensitive to Environmental Toxins Associated with Parkinson’s Disease

    Drosophila DJ-1 Mutants Are Selectively Sensitive to Environmental Toxins Associated with Parkinson’s Disease por Marc C. Meulener, Alexander J. Whitworth, Cecilia E. Armstrong‐Gold, Patrizia Rizzu, Peter Heutink, Paul D. Wes, Leo J. Pallanck, Nancy M. Bonini

    Publicado em 2005
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  3. 3
    Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes

    Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes por Katherine Fodder, Megha Murthy, Patrizia Rizzu, Christina E. Toomey, Rahat Hasan, Jack Humphrey, Towfique Raj, Katie Lunnon, Jonathan Mill, Peter Heutink, Tammaryn Lashley, Conceição Bettencourt

    Publicado em 2023
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  4. 4
    Proteomic and Functional Analyses Reveal a Mitochondrial Dysfunction in P301L Tau Transgenic Mice

    Proteomic and Functional Analyses Reveal a Mitochondrial Dysfunction in P301L Tau Transgenic Mice por Della David, Susanne Hauptmann, Isabel Scherping, Katrin Schuessel, Uta Keil, Patrizia Rizzu, Rivka Ravid, Stefan Dröse, Ulrich Brandt, Wernér E.G. Müller, Anne Eckert, Jürgen Götz

    Publicado em 2005
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  5. 5
    Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families

    Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families por Peter Heutink, M Stevens, Patrizia Rizzu, Egbert Bakker, J. M. Kros, Aad Tibben, Martinus F. Niermeijer, Cornelia M. van Duijn, B. A. Oostra, John C. van Swieten

    Publicado em 1997
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  6. 6
    DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism

    DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism por Vincenzo Bonifati, Patrizia Rizzu, Ferdinando Squitieri, Elmar Krieger, N. Vanacore, John C. van Swieten, Alexis Brice, Cornelia M. van Duijn, Ben A. Oostra, G. Meco, Peter Heutink

    Publicado em 2003
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  7. 7
    C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers

    C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers por Patrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, Emily M. Lynes, Melissa Castillo-Lizardo, Ashutosh Dhingra, Elwira Pyż, Markus A. Hobert, Matthis Synofzik, Javier Simón‐Sánchez, Margherita Francescatto, Peter Heutink

    Publicado em 2016
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  8. 8
    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects por Cornelis Blauwendraat, Carlo Wilke, Javier Simón‐Sánchez, Iris E. Jansen, Anika Reifschneider, Anja Capell, Christian Haass, Melissa Castillo-Lizardo, Saskia Biskup, Walter Maetzler, Patrizia Rizzu, Peter Heutink, Matthis Synofzik

    Publicado em 2017
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  9. 9
    Blood–brain barrier P-glycoprotein function in healthy subjects and Alzheimer's disease patients: effect of polymorphisms in the ABCB1 gene

    Blood–brain barrier P-glycoprotein function in healthy subjects and Alzheimer's disease patients: effect of polymorphisms in the ABCB1 gene por Daniëlle ME van Assema, Mark Lubberink, Patrizia Rizzu, John C. van Swieten, Robert C. Schuit, Jonas Eriksson, Philip Scheltens, Matthias J. Koepp, Adriaan A. Lammertsma, Bart N.M. van Berckel

    Publicado em 2012
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  10. 10
    DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathway

    DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathway por Hossein Aleyasin, Maxime W.C. Rousseaux, Paul C. Marcogliese, Sarah J. Hewitt, Isabella Irrcher, Alvin Joselin, Mohammad Parsanejad, Raymond H. Kim, Patrizia Rizzu, Steve Callaghan, Ruth S. Slack, Tak W. Mak, David S. Park

    Publicado em 2010
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  11. 11
    High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands

    High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands por Patrizia Rizzu, John C. van Swieten, Marijke Joosse, Masato Hasegawa, Martijn Stevens, Aad Tibben, Martinus F. Niermeijer, Marcel Hillebrand, Rivka Ravid, Ben A. Oostra, Michel Goedert, Cornelia M. van Duijn, Peter Heutink

    Publicado em 1999
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  12. 12
    TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

    TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations por Harro Seelaar, Helenius J. Schelhaas, Asma Azmani, Benno Küsters, S. Rosso, Daniëlle Majoor‐Krakauer, M. C. de Rijik, Patrizia Rizzu, M. ten Brummelhuis, Pieter A. van Doorn, Wouter Kamphorst, Rob Willemsen, John C. van Swieten

    Publicado em 2007
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  13. 13
    Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

    Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia por Elise G.P. Dopper, Serge A.R.B. Rombouts, Lize C. Jiskoot, Tom den Heijer, J. Roos A. de Graaf, Inge de Koning, Anke R. Hammerschlag, Harro Seelaar, William W. Seeley, Ilya M. Veer, Mark A. van Buchem, Patrizia Rizzu, John C. van Swieten

    Publicado em 2013
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  14. 14
    Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

    Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia por Elise G.P. Dopper, Serge A.R.B. Rombouts, Lize C. Jiskoot, Tom den Heijer, J. Roos A. de Graaf, Inge de Koning, Anke R. Hammerschlag, Harro Seelaar, William W. Seeley, Ilya M. Veer, Mark A. van Buchem, Patrizia Rizzu, John C. van Swieten

    Publicado em 2014
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  15. 15
    A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia

    A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia por Ana I. Seixas, Joana R. Loureiro, Cristina Costa, Andrés Ordóñez‐Ugalde, Hugo Marcelino, Cláudia Oliveira, José L. Loureiro, Ashutosh Dhingra, Eva Brandão, Vítor Tedim Cruz, Ângela Timóteo, Beatriz Quintáns, Guy A. Rouleau, Patrizia Rizzu, Ángel Carracedo, José Bessa, Peter Heutink, Jorge Sequeiros, María Jesús Sobrido, Paula Coutinho, Isabel Silveira

    Publicado em 2017
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  16. 16
    Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease

    Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease por Xianjun Dong, Zhixiang Liao, David Gritsch, Yavor Hadzhiev, Yunfei Bai, Joseph J. Locascio, Boris Guennewig, Ganqiang Liu, Cornelis Blauwendraat, Tao Wang, Charles H. Adler, John C. Hedreen, Richard L. M. Faull, Matthew P. Frosch, Peter T. Nelson, Patrizia Rizzu, Antony A. Cooper, Peter Heutink, Thomas G. Beach, John S. Mattick, Ferenc Müller, Clemens R. Scherzer

    Publicado em 2018
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  17. 17
    Genome-wide association study confirms extant PD risk loci among the Dutch

    Genome-wide association study confirms extant PD risk loci among the Dutch por Javier Simón‐Sánchez, Jacobus J. van Hilten, Bart van de Warrenburg, Bart Post, Henk W. Berendse, Sampath Arepalli, Dena G Hernandez, Rob M.A. de Bie, Daan C. Velseboer, Hans Scheffer, Bas R. Bloem, Karin D van Dijk, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, Patrizia Rizzu, Zoltán Bochdanovits, Andrew B. Singleton, Peter Heutink

    Publicado em 2011
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  18. 18
    β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson’s disease

    β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson’s disease por Shuchi Mittal, Kjetil Bjørnevik, Doo Soon Im, Adrian Flierl, Xianjun Dong, Joseph J. Locascio, Kristine M. Abo, Elizabeth Long, Ming Jin, Bing Xu, Yang Xiang, Jean‐Christophe Rochet, Anders Engeland, Patrizia Rizzu, Peter Heutink, Tim Bartels, Dennis J. Selkoe, Barbara J. Caldarone, Marcie A. Glicksman, Vikram Khurana, Birgitt Schüle, David S. Park, Trond Riise, Clemens R. Scherzer

    Publicado em 2017
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  19. 19
    The Netherlands Twin Register Biobank: A Resource for Genetic Epidemiological Studies

    The Netherlands Twin Register Biobank: A Resource for Genetic Epidemiological Studies por Gonneke Willemsen, Eco J. C. de Geus, Meike Bartels, C.E.M. van Beijsterveldt, Andy Brooks, G. Frederique Estourgie-van Burk, Douglas A. Fugman, Chantal Hoekstra, Jouke‐Jan Hottenga, Kees Kluft, Piet Meijer, Grant W. Montgomery, Patrizia Rizzu, David Sondervan, August B. Smit, Sabine Spijker, H. Eka D. Suchiman, Jay A. Tischfield, Thomas Lehner, P. Eline Slagboom, Dorret I. Boomsma

    Publicado em 2010
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  20. 20
    Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics

    Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamics por Isabella Irrcher, Hossein Aleyasin, Erin L. Seifert, Sarah J. Hewitt, Shivani Chhabra, Melissa Phillips, A. Kathrin Lutz, Maxime W.C. Rousseaux, Lisa Bevilacqua, Arezu Jahani‐Asl, Steve Callaghan, Jason G. MacLaurin, Konstanze F. Winklhofer, Patrizia Rizzu, Peter Rippstein, Raymond H. Kim, C.X. Chen, Edward A. Fon, Ruth S. Slack, Mary‐Ellen Harper, Heidi M. McBride, Tak W. Mak, David S. Park

    Publicado em 2010
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