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1-3 of 3
Keywords: DYRK1A
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Journal Articles
Yushi Redhead, Dorota Gibbins, Eva Lana-Elola, Sheona Watson-Scales, Lisa Dobson, Matthias Krause, Karen J. Liu, Elizabeth M. C. Fisher, Jeremy B. A. Green, Victor L. J. Tybulewicz
Journal:
Development
Development (2023) 150 (8): dev201077.
Published: 26 April 2023
... and an associated mouse genetic mapping panel, we demonstrate that four Hsa21-orthologous regions of mouse chromosome 16 contain dosage-sensitive genes that cause the DS craniofacial phenotype, and identify one of these causative genes as Dyrk1a . We show that the earliest and most severe defects in Dp1Tyb skulls...
Includes: Supplementary data
Journal Articles
Helen Rankin Willsey, Yuxiao Xu, Amanda Everitt, Jeanselle Dea, Cameron R. T. Exner, A. Jeremy Willsey, Matthew W. State, Richard M. Harland
Journal:
Development
Development (2020) 147 (21): dev189290.
Published: 22 June 2020
...Helen Rankin Willsey; Yuxiao Xu; Amanda Everitt; Jeanselle Dea; Cameron R. T. Exner; A. Jeremy Willsey; Matthew W. State; Richard M. Harland; Sally Dunwoodie; John Wallingford ABSTRACT DYRK1A [dual specificity tyrosine-(Y)-phosphorylation-regulated kinase 1 A] is a high-confidence autism risk gene...
Includes: Supplementary data
Journal Articles
In collection:
Neural development
Mirja N. Shaikh, Francisco Gutierrez-Aviño, Jordi Colonques, Julian Ceron, Barbara Hämmerle, Francisco J. Tejedor
Journal:
Development
Development (2016) 143 (17): 3195–3205.
Published: 1 September 2016
... show that minibrain ( mnb ), the Drosophila ortholog of the Down syndrome candidate gene DYRK1A , is transiently expressed in newborn neuronal precursors known as ganglion cells (GCs). Mnb promotes the cell cycle exit of GCs through a dual mechanism that regulates the expression of the cyclin-dependent...
Includes: Supplementary data