Central neurogenetic signatures of the visuomotor integration system
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/8033
comunitat-uji-handle3:10234/8636
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Título
Central neurogenetic signatures of the visuomotor integration systemAutoría
Fecha de publicación
2020Editor
National Academy of SciencesISSN
0027-8424; 1091-6490Cita bibliográfica
Elisenda Bueichekú, Maite Aznárez-Sanado, Ibai Diez, Federico d’Oleire Uquillas, Laura Ortiz-Terán, Abid Y. Qureshi, Maria Suñol, Silvia Basaia, Elena Ortiz-Terán, Maria A. Pastor, Jorge Sepulcre. Central neurogenetic signatures of the visuomotor integration system. Proceedings of the National Academy of Sciences. Mar 2020, 117 (12) 6836-6843; DOI: 10.1073/pnas.1912429117Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://www.pnas.org/content/117/12/6836.shortVersión
info:eu-repo/semantics/submittedVersionPalabras clave / Materias
Resumen
Visuomotor impairments characterize numerous neurological disorders and neurogenetic syndromes, such as autism spectrum disorder (ASD) and Dravet, Fragile X, Prader–Willi, Turner, and Williams syndromes. Despite recent ... [+]
Visuomotor impairments characterize numerous neurological disorders and neurogenetic syndromes, such as autism spectrum disorder (ASD) and Dravet, Fragile X, Prader–Willi, Turner, and Williams syndromes. Despite recent advances in systems neuroscience, the biological basis underlying visuomotor functional impairments associated with these clinical conditions is poorly understood. In this study, we used neuroimaging connectomic approaches to map the visuomotor integration (VMI) system in the human brain and investigated the topology approximation of the VMI network to the Allen Human Brain Atlas, a whole-brain transcriptome-wide atlas of cortical genetic expression. We found the genetic expression of four genes—TBR1, SCN1A, MAGEL2, and CACNB4—to be prominently associated with visuomotor integrators in the human cortex. TBR1 gene transcripts, an ASD gene whose expression is related to neural development of the cortex and the hippocampus, showed a central spatial allocation within the VMI system. Our findings delineate gene expression traits underlying the VMI system in the human cortex, where specific genes, such as TBR1, are likely to play a central role in its neuronal organization, as well as on specific phenotypes of neurogenetic syndromes. [-]
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Proceedings of the National Academy of Sciences, 2020, vol. 117, no 12Derechos de acceso
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