Risultati della ricerca - Astrid Vallès

  • Mostra 1 - 9 risultati su 9
Raffina i risultati
  1. 1
    Oxidative stress, prefrontal cortex hypomyelination and cognitive symptoms in schizophrenia

    Oxidative stress, prefrontal cortex hypomyelination and cognitive symptoms in schizophrenia di Dorien A. Maas, Astrid Vallès, Gerard J.M. Martens

    Pubblicazione 2017
    Testo Testo
    Revisão
    Aggiungi alla lista
    Salvato in:
  2. 2
    AAV5-miHTT Gene Therapy Demonstrates Sustained Huntingtin Lowering and Functional Improvement in Huntington Disease Mouse Models

    AAV5-miHTT Gene Therapy Demonstrates Sustained Huntingtin Lowering and Functional Improvement in Huntington Disease Mouse Models di Elisabeth A. Spronck, Cynthia Brouwers, Astrid Vallès, Martin de Haan, Harald Petry, S J van Deventer, Pavlina Konstantinova, Melvin M. Evers

    Pubblicazione 2019
    Testo Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  3. 3
    AAV5-miHTT Lowers Huntingtin mRNA and Protein without Off-Target Effects in Patient-Derived Neuronal Cultures and Astrocytes

    AAV5-miHTT Lowers Huntingtin mRNA and Protein without Off-Target Effects in Patient-Derived Neuronal Cultures and Astrocytes di Sonay Keskin, Cynthia Brouwers, Marina Sogorb-González, Raygene Martier, Josse A. Depla, Astrid Vallès, S J van Deventer, Pavlina Konstantinova, Melvin M. Evers

    Pubblicazione 2019
    Testo Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  4. 4
    Interneuron hypomyelination is associated with cognitive inflexibility in a rat model of schizophrenia

    Interneuron hypomyelination is associated with cognitive inflexibility in a rat model of schizophrenia di Dorien A. Maas, Vivian D. Eijsink, Marcia Spoelder, Josephus A. van Hulten, Peter De Weerd, Judith R. Homberg, Astrid Vallès, Brahim Nait‐Oumesmar, Gerard J.M. Martens

    Pubblicazione 2020
    Testo Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  5. 5
    Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington disease models

    Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington disease models di Marina Sogorb-González, Christian Landles, Nicholas S. Caron, Anouk Stam, Georgina F Osborne, Michael R. Hayden, David Howland, Sander van Deventer, Gillian P. Bates, Astrid Vallès, Melvin M. Evers

    Pubblicazione 2024
    Testo Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  6. 6
    Intrastriatal Administration of AAV5-miHTT in Non-Human Primates and Rats Is Well Tolerated and Results in miHTT Transgene Expression in Key Areas of Huntington Disease Pathology

    Intrastriatal Administration of AAV5-miHTT in Non-Human Primates and Rats Is Well Tolerated and Results in miHTT Transgene Expression in Key Areas of Huntington Disease Pathology di Elisabeth A. Spronck, Astrid Vallès, Margit H. Lampen, Paula S. Montenegro-Miranda, Sonay Keskin, Liesbeth Heijink, Melvin M. Evers, Harald Petry, S. J. H. Van Deventer, Pavlina Konstantinova, Martin de Haan

    Pubblicazione 2021
    Testo Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  7. 7
    White matter structure and myelin-related gene expression alterations with experience in adult rats

    White matter structure and myelin-related gene expression alterations with experience in adult rats di Cassandra Sampaio‐Baptista, Astrid Vallès, Alexandre A. Khrapitchev, Guus Akkermans, Anderson M. Winkler, Sean Foxley, Nicola R. Sibson, Mark Roberts, Karla L. Miller, Mathew E. Diamond, Gerard J.M. Martens, Peter De Weerd, Heidi Johansen‐Berg

    Pubblicazione 2020
    Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  8. 8
    AAV5-miHTT Gene Therapy Demonstrates Broad Distribution and Strong Human Mutant Huntingtin Lowering in a Huntington’s Disease Minipig Model

    AAV5-miHTT Gene Therapy Demonstrates Broad Distribution and Strong Human Mutant Huntingtin Lowering in a Huntington’s Disease Minipig Model di Melvin M. Evers, Jana Miniarikova, Štefan Juhás, Astrid Vallès, Božena Bohuslavová, Jana Juhásová, Helena Kupcová Skalníková, Petr Vodička, Ivona Valeková, Cynthia Brouwers, Bas Blits, Jacek Lubelski, Hana Kovářová, Zdeňka Ellederová, S J van Deventer, Harald Petry, Jan Motlík, Pavlina Konstantinova

    Pubblicazione 2018
    Testo
    Artigo
    Aggiungi alla lista
    Salvato in:
  9. 9
    Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability

    Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability di Marjolein H. Willemsen, Astrid Vallès, Laurens A. M. H. Kirkels, Mathilde Mastebroek, Nikkie Olde Loohuis, Aron Kos, W.M. Wissink-Lindhout, Arjan P.M. de Brouwer, Willy M. Nillesen, Rolph Pfundt, Muriel Holder‐Espinasse, Louis Vallée, Joris Andrieux, Marjolein C. Coppens‐Hofman, Hanneke Rensen, Ben C.J. Hamel, Hans van Bokhoven, Armaz Aschrafi, Tjitske Kleefstra

    Pubblicazione 2011
    Testo
    Artigo
    Aggiungi alla lista
    Salvato in:

Strumenti per la ricerca: