Hasil Pencarian - Peter Heutink

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  1. 1
    Transcription start site signal profiling improves transposable element RNA expression analysis at locus-level

    Transcription start site signal profiling improves transposable element RNA expression analysis at locus-level oleh Natalia Savytska, Peter Heutink, Vikas Bansal

    Diterbitkan 2022-10-01
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  2. 2
    Epigenetic Age Acceleration in Frontotemporal Lobar Degeneration: A Comprehensive Analysis in the Blood and Brain

    Epigenetic Age Acceleration in Frontotemporal Lobar Degeneration: A Comprehensive Analysis in the Blood and Brain oleh Megha Murthy, Patrizia Rizzu, Peter Heutink, Jonathan Mill, Tammaryn Lashley, Conceição Bettencourt

    Diterbitkan 2023-07-01
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  3. 3
    Genome-wide prediction of functional gene-gene interactions inferred from patterns of genetic differentiation in mice and men.

    Genome-wide prediction of functional gene-gene interactions inferred from patterns of genetic differentiation in mice and men. oleh Zoltán Bochdanovits, David Sondervan, Sophie Perillous, Toos van Beijsterveldt, Dorret Boomsma, Peter Heutink

    Diterbitkan 2008-02-01
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  4. 4
    Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways.

    Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways. oleh Iraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, Wouter Kamphorst, Rivka Ravid, John C van Swieten, Peter Heutink

    Diterbitkan 2009-08-01
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  5. 5
    Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.

    Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. oleh Javier Simón-Sánchez, Harro Seelaar, Zoltán Bochdanovits, Dorly J H Deeg, John C van Swieten, Peter Heutink

    Diterbitkan 2009-01-01
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  6. 6
    Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening

    Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening oleh Ibrahim Boussaad, Gérald Cruciani, Silvia Bolognin, Paul Antony, Claire M. Dording, Yong-Jun Kwon, Peter Heutink, Eugenio Fava, Jens C. Schwamborn, Rejko Krüger

    Diterbitkan 2021-01-01
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  7. 7
    Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21–22

    Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21–22 oleh Armand Savioz, Beat M Riederer, Peter Heutink, Patrizia Rizzu, Markus Tolnay, Enikö Kövari, Alphonse Probst, I.rène M Riederer, Constantin Bouras, Geneviève Leuba

    Diterbitkan 2003-02-01
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  8. 8
    iPS Cell-Based Model for MAPT Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression

    iPS Cell-Based Model for MAPT Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression oleh Tabea Strauß, Tabea Strauß, Amir Marvian-Tayaranian, Amir Marvian-Tayaranian, Eldem Sadikoglou, Ashutosh Dhingra, Florian Wegner, Florian Wegner, Dietrich Trümbach, Wolfgang Wurst, Wolfgang Wurst, Wolfgang Wurst, Peter Heutink, Peter Heutink, Sigrid C. Schwarz, Sigrid C. Schwarz, Sigrid C. Schwarz, Günter U. Höglinger, Günter U. Höglinger, Günter U. Höglinger, Günter U. Höglinger

    Diterbitkan 2021-08-01
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  9. 9
    <i>PLA2G6</i> Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism

    <i>PLA2G6</i> Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism oleh Anamika Giri, Gamze Guven, Hasmet Hanagasi, Ann-Kathrin Hauser, Nihan Erginul-Unaltuna, Basar Bilgic, Hakan Gurvit, Peter Heutink, Thomas Gasser, Ebba Lohmann, Javier Simón-Sánchez

    Diterbitkan 2016-03-01
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  10. 10
    Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's Disease.

    Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's Disease. oleh Anke A Dijkstra, Angela Ingrassia, Renee X de Menezes, Ronald E van Kesteren, Annemieke J M Rozemuller, Peter Heutink, Wilma D J van de Berg

    Diterbitkan 2015-01-01
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  11. 11
    Trehalose improves human fibroblast deficits in a new CHIP-mutation related ataxia.

    Trehalose improves human fibroblast deficits in a new CHIP-mutation related ataxia. oleh Maria Jose Casarejos, Juan Perucho, Jose Luis López-Sendón, Justo García de Yébenes, Conceição Bettencourt, Ana Gómez, Carolina Ruiz, Peter Heutink, Patrizia Rizzu, Maria Angeles Mena

    Diterbitkan 2014-01-01
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  12. 12
    FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in Brain.

    FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in Brain. oleh Thais S Rizzi, Sophie van der Sluis, Catherine Derom, Evert Thiery, Ronald E van Kesteren, Nele Jacobs, Sofie Van Gestel, Robert Vlietinck, Matthijs Verhage, Peter Heutink, Danielle Posthuma

    Diterbitkan 2013-01-01
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  13. 13
    Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interference

    Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interference oleh Daniel Heinzer, Merve Avar, Daniel Patrick Pease, Ashutosh Dhingra, Jiang-An Yin, Elke Schaper, Berre Doğançay, Marc Emmenegger, Anna Spinelli, Kevin Maggi, Andra Chincisan, Simon Mead, Simone Hornemann, Peter Heutink, Adriano Aguzzi

    Diterbitkan 2021-10-01
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  14. 14
    Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interference.

    Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interference. oleh Daniel Heinzer, Merve Avar, Daniel Patrick Pease, Ashutosh Dhingra, Jiang-An Yin, Elke Schaper, Berre Doğançay, Marc Emmenegger, Anna Spinelli, Kevin Maggi, Andra Chincisan, Simon Mead, Simone Hornemann, Peter Heutink, Adriano Aguzzi

    Diterbitkan 2021-10-01
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  15. 15
    Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.

    Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients. oleh Gamze Guven, Ebba Lohmann, Jose Bras, J Raphael Gibbs, Hakan Gurvit, Basar Bilgic, Hasmet Hanagasi, Patrizia Rizzu, Peter Heutink, Murat Emre, Nihan Erginel-Unaltuna, Walter Just, John Hardy, Andrew Singleton, Rita Guerreiro

    Diterbitkan 2016-01-01
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  16. 16
    Resequencing three candidate genes for major depressive disorder in a Dutch cohort.

    Resequencing three candidate genes for major depressive disorder in a Dutch cohort. oleh Eva C Verbeek, Marianna R Bevova, Zoltán Bochdanovits, Patrizia Rizzu, Ingrid M C Bakker, Tiny Uithuisje, Eco J De Geus, Johannes H Smit, Brenda W Penninx, Dorret I Boomsma, Witte J G Hoogendijk, Peter Heutink

    Diterbitkan 2013-01-01
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  17. 17
    A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.

    A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. oleh Eva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, Zoltán Bochdanovits, Patrizia Rizzu, David Sondervan, Gonneke Willemsen, Eco J de Geus, Johannes H Smit, Brenda W Penninx, Dorret I Boomsma, Witte J G Hoogendijk, Peter Heutink

    Diterbitkan 2012-01-01
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  18. 18
    Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.

    Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. oleh Javier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, Maria Martinez, Claudia Schulte, Peter Holmans, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium, Thomas Gasser, John Hardy, Andrew B Singleton, Nicholas W Wood, Alexis Brice, Peter Heutink, Nigel Williams, Huw R Morris

    Diterbitkan 2012-01-01
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  19. 19
    A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes

    A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes oleh Kevin Menden, Margherita Francescatto, Tenzin Nyima, Cornelis Blauwendraat, Ashutosh Dhingra, Melissa Castillo-Lizardo, Noémia Fernandes, Lalit Kaurani, Deborah Kronenberg-Versteeg, Burcu Atasu, Eldem Sadikoglou, Barbara Borroni, Salvador Rodriguez-Nieto, Javier Simon-Sanchez, Andre Fischer, David Wesley Craig, Manuela Neumann, Stefan Bonn, Patrizia Rizzu, Peter Heutink

    Diterbitkan 2023-12-01
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  20. 20
    Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing

    Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing oleh Mafalda Raposo, Conceição Bettencourt, Ana Rosa Vieira Melo, Ana F. Ferreira, Isabel Alonso, Paulo Silva, João Vasconcelos, Teresa Kay, Maria Luiza Saraiva-Pereira, Marta D. Costa, Daniela Vilasboas-Campos, Bruno Filipe Bettencourt, Jácome Bruges-Armas, Henry Houlden, Peter Heutink, Laura Bannach Jardim, Jorge Sequeiros, Patrícia Maciel, Manuela Lima

    Diterbitkan 2022-01-01
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