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The molecular mechanisms that lead to the cognitive defects characteristic of Down syndrome (DS), the most frequent cause of mental retardation, have remained elusive. Here we use a transgenic DS mouse model to show that DYRK1A gene dosage imbalance deregulates chromosomal clusters of genes located ...
ORGANISM(S): Mus musculus 
DYRK1A is a protein kinase whose dysregulation is linked to disease in humans. On the one side, its overexpression in trisomy 21 has been linked to certain Down syndrome pathological traits, while inactivating mutations in just one allele that hinders its function are responsible for a rare clinical...
ORGANISM(S): Homo sapiens (Human) 
2019-07-15 | PXD011925 | Pride
DYRK1A is a dosage-sensitive protein kinase that fulfills key roles during development and in tissue homeostasis, and its dysregulation results in human pathologies. DYRK1A is present in both the nucleus and cytoplasm of mammalian cells, although its nuclear function remains unclear. Genome-wide ana...
ORGANISM(S): Homo sapiens 
This SuperSeries is composed of the following subset Series:; GSE14021: Transcriptional analysis of E12.5 telencephalon from 152F7 transgenic mouse; GSE14030: Transcriptional analysis of murine neurobastoma N18 cell line transfected with a pAd-Dyrk1a vector Experiment Overall Design: Refer to indivi...
ORGANISM(S): Mus musculus 
Transcription profiling of transgenic down syndrome mouse model to show the role of DYRK1A gene. The molecular mechanisms that lead to the cognitive defects characteristic of Down syndrome (DS), the most frequent cause of mental retardation, have remained elusive. Here we use a transgenic DS mouse m...
ORGANISM(S): Mus musculus 
The uploaded data are described within "DYRK1A promotes nuclear F-actin assembly to effect DSB repair metabolism". Peptides from RPE1 epithelial cells with either, over expression of DYRK1A, normal expression of DYRK1A, or knockout of DYRK1A were labeled with TMTpro-16 reagents and phosphopeptides e...
ORGANISM(S): Homo sapiens (Human) 
2024-07-19 | PXD031714 | Pride
Dyrk1A deficiency is linked to various neurodevelopmental disorders, including developmental delays and autism spectrum disorders (ASD). Haploinsufficiency of Dyrk1a in mice leads to ASD-related phenotypes, although key pathological mechanisms remain unclear. In addition, human DYRK1A mutations have...
ORGANISM(S): Mus musculus (Mouse) 
2024-12-04 | PXD050100 | Pride
Expression data in the cerebral cortex of postnatal Dyrk1a+/+ and Dyrk1a+/- mice
Role of DYRK1A in MPN
Here we performed a detailed investigation to delineate the role of DYRK1A in glioblastoma, using both pharmacological and genetic tools combined with global phosphoproteomics. Our data show that DYRK1A inhibitors affect a much broader proportion of the phosphoproteome than DYRK1A knockdown. By over...
ORGANISM(S): Homo sapiens (Human) 
2021-04-22 | PXD020441 | Pride
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