Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome-Reference-Cited by-同舟云学术

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Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome

Published:2019-07 Issue: Volume:127 Page:210-222
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Arranz Juan,Balducci Elisa,Arató Krisztina,Sánchez-Elexpuru Gentzane,Najas Sònia,Parras Alberto,Rebollo Elena,Pijuan Isabel,Erb Ionas,Verde Gaetano^ORCID,Sahun Ignasi,Barallobre Maria J.,Lucas José J.,Sánchez Marina P.,de la Luna Susana^ORCID,Arbonés Maria L.^ORCID

Funder

Spanish Ministry of Economia, Industria y Competitividad

Secretariat of Universities and Research-Generalitat de Catalunya

Fundación Alicia Koplowitz

MINECO

Centro de Excelencia Severo Ochoa Programme

CERCA Programme

Generalitat de Catalunya

National Institute of Neurological Disorders and Stroke of the National Institutes of Health

Spanish Instituto de Salud Carlos III

Fundación Conchita Rábago

Publisher

Elsevier BV

Subject

Neurology

Reference70 articles.

1. DYRK1A accumulates in splicing speckles through a novel targeting signal and induces speckle disassembly;Alvarez;J. Cell Sci.,2003

2. DYRK family of protein kinases: evolutionary relationships, biochemical properties, and functional roles;Aranda;FASEB J.,2011

3. Impaired spatial learning strategies and novel object recognition in mice haploinsufficient for the dual specificity tyrosine-regulated kinase-1A (Dyrk1A);Arque;PLoS One,2008

4. DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson's disease;Barallobre;Cell Death Dis.,2014

5. DYRK1A: a potential drug target for multiple Down syndrome neuropathologies;Becker;CNS Neurol. Disord. Drug Targets,2014

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1. Skeletal health in DYRK1A syndrome;Frontiers in Neuroscience;2024-09-06

2. Heterozygous Nexmif female mice demonstrate mosaic NEXMIF expression, autism-like behaviors, and abnormalities in dendritic arborization and synaptogenesis;Heliyon;2024-02

3. Discovery of a Novel DYRK1A Mutation (c.524del) in Intellectual Development Disorder Autosomal Dominant 7 (MRD7): A Comprehensive Case Analysis;Case Reports in Genetics;2024-01

4. Loss of the DYRK1A Protein Kinase Results in the Reduction in Ribosomal Protein Gene Expression, Ribosome Mass and Reduced Translation;Biomolecules;2023-12-25

5. Interneuron migration defects during corticogenesis contribute toDyrk1ahaploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations;2023-11-10

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