Results 1 to 10 of about 9,925 (218)

DYRK1A roles in human neural progenitors [PDF]

open access: yesFrontiers in Neuroscience
IntroductionMutations in dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) represent one of the most prevalent monogenic causes of neurodevelopmental disorders (NDDs), often associated with intellectual developmental disorder and ...
Jeremie Courraud   +30 more
doaj   +4 more sources

DYRK1A modulates fear memory formation via epigenetic modification [PDF]

open access: yesMolecular Brain
Fear memory formation is crucial for survival, with the hippocampus playing a central role. This study investigates the behavioral and molecular aspects of fear memory formation, focusing on Dual-specificity tyrosine phosphorylation-regulated kinase 1 A (
Dae-Si Kang, Ja Wook Koo
doaj   +4 more sources

Genetic knockdown of DYRK1A attenuates cognitive impairment, Aβ pathology, tauopathy and neuroinflammatory responses in mouse models of AD [PDF]

open access: yesFrontiers in Immunology
IntroductionDual specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is associated with the pathoprogression of neurodevelopmental and neurodegenerative disorders.
Hyun-ju Lee   +24 more
doaj   +2 more sources

DYRK1A in the physiology and pathology of the neuron-astrocyte axis [PDF]

open access: yesFrontiers in Neuroscience
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a dosage-sensitive kinase with critical roles in the neuron-astrocyte axis. During brain development, DYRK1A ensures the proper number of differentiated neurons and astrocytes.
Pablo Cisternas   +5 more
doaj   +2 more sources

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

open access: yesNeurobiology of Disease, 2014
Cognitive deficits in Down syndrome (DS) have been linked to increased synaptic inhibition, leading to an imbalance of excitation/inhibition (E/I). Various mouse models and studies from human brains have implicated an HSA21 gene, the serine/threonine ...
Benoit Souchet   +2 more
exaly   +3 more sources

Clinical and molecular overlap between nucleotide excision repair (NER) disorders and DYRK1A haploinsufficiency syndrome [PDF]

open access: yesFrontiers in Neuroscience
Nucleotide excision repair (NER) disorders are genetic conditions caused by defects in the pathway responsible for repairing DNA lesions due to UV radiation. These defects lead to a variety of heterogeneous disorders, including Cockayne syndrome (CS) and
Nicolas Le May   +16 more
doaj   +2 more sources

Identification of FAM53C as a cytosolic-anchoring inhibitory binding protein of the kinase DYRK1A

open access: yesLife Science Alliance, 2023
A previously uncharacterized protein, FAM53C, is identified as a binding partner for the kinase DYRK1A involved in numerous neurodevelopmental disorders, such as Down syndrome and autism spectrum disorder.
Yoshihiko Miyata, Eisuke Nishida
doaj   +1 more source

Optimization and validation of a DYRK1A TR-FRET assay for high-throughput screening

open access: yesMethodsX, 2021
Due to its role in brain development, the DYRK1A kinase (dual-specificity tyrosine phosphorylation-regulated kinase 1a) has been proposed as a drug target for Down syndrome, and diseases associated with neurodegeneration including Alzheimer's and ...
Michael Tarpley   +3 more
doaj   +1 more source

Global phosphoproteomics reveals DYRK1A regulates CDK1 activity in glioblastoma cells

open access: yesCell Death Discovery, 2021
Both tumour suppressive and oncogenic functions have been reported for dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A). Herein, we performed a detailed investigation to delineate the role of DYRK1A in glioblastoma.
Ariadna Recasens   +13 more
doaj   +1 more source

Genetic landscape of autism spectrum disorder in Vietnamese children [PDF]

open access: yes, 2020
Autism spectrum disorder (ASD) is a complex disorder with an unclear aetiology and an estimated global prevalence of 1%. However, studies of ASD in the Vietnamese population are limited.
Bui, HTP   +12 more
core   +2 more sources

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