Accès ouvert
2026
conference-abstract
OpenAlex
Maja Rebecca Adel, Ester Antón-Galindo, Manuel Tobías-Olave, Ana Martos-Guillamet et autres
Background The splicing factor RBFOX1 exerts pleiotropic effects on numerous neurodevelopmental and psychiatric disorders. Previous studies by our group in two zebrafish lines showed that mutations in rbfox1 lead to hyperactivity, increased thigmotaxis, and social impairments. However, the biological mechanisms underlying these …
at, es, gb, ca
(code pays fourni par la source)
Accès ouvert
2026
article
OpenAlex
Jose Vicente Torres-Pérez, Adele Leggieri, Xian Wang, Aine Kehoe et autres
Williams syndrome (WS) is a multifaceted developmental disorder characterized by a spectrum of physical and intellectual traits. Individuals with WS exhibit friendly, impulsive, and hyper-social behaviours, often coupled with anxiety. WS is caused by a hemizygous microdeletion on chromosome 7q11.23. Among the …
es, gb
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Adele Leggieri, Judit García‐González, Saeedeh Hosseinian, Peter Ashdown et autres
Mutations in the RBFOX1 gene are associated with psychiatric disorders but how RBFOX1 influences psychiatric disorder vulnerability remains unclear. Recent studies showed that RBFOX proteins mediate the alternative splicing of PAC1, a critical HPA axis activator. Further, RBFOX1 dysfunction is linked to …
gb, us, es
(code pays fourni par la source)
Accès ouvert
2025
article
OpenAlex
Courtney Hillman, Barbara Dotto Fontana, Tamara G. Amstislavskaya, М. А. Gorbunova et autres
The reproducibility crisis in bioscience, characterized by inconsistent study results, impedes our understanding of biological processes. Global collaborative studies offer a unique solution to this problem. Here, we present a global collaboration using the zebrafish (Danio rerio) novel tank test, a popular …
gb, us, br, ru, au, cl, ar, az, pt, cn
(code pays fourni par la source)
2025
conference-abstract
OpenAlex
Xian Wang, Oliver Haworth, Sayka Barry, Adele Leggieri et autres
Accès ouvert
2025
preprint
OpenAlex
Roberta Bilardo, Adele Leggieri, Francesca Tomatis, Federico Traldi et autres
The development of effective neurological treatments remains a challenge due to the low permeation across the blood-brain barrier (BBB). The use of nanoparticles for brain drug delivery is promising, but the level of BBB crossing remains low, typically around 0.5-3%. We report …
gb, pt, fr
(code pays fourni par la source)
Accès ouvert
2025
preprint
OpenAlex
Roberta Bilardo, Adele Leggieri, Francesca Tomatis, Federico Traldi et autres
The development of effective neurological treatments remains a challenge due to the low permeation across the blood-brain barrier (BBB). The use of nanoparticles for brain drug delivery is promising, but the level of BBB crossing remains low, typically around 0.5-3%. We report …
gb, pt, fr
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Matthew O. Parker, Courtney Hillman, Barbara Dotto Fontana, Tamara G. Amstislavskaya et autres
gb, br, ru, au, cl, us, ar, Somalie, ag, pt, cn
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Adele Leggieri, Judit García‐González, Saeedeh Hosseinian, Peter Ashdown et autres
ABSTRACT Mutations in the RBFOX1 gene are associated with psychiatric disorders but how RBFOX1 influences psychiatric disorder vulnerability remains unclear. Recent studies showed that RBFOX proteins mediate the alternative splicing of PAC1, a critical HPA axis activator. Further, RBFOX1 dysfunction is linked …
gb, us, es
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Ester Antón-Galindo, Maja R. Adel, Judit García‐González, Adele Leggieri et autres
Abstract RBFOX1 is a highly pleiotropic gene that contributes to several psychiatric and neurodevelopmental disorders. Both rare and common variants in RBFOX1 have been associated with several psychiatric conditions, but the mechanisms underlying the pleiotropic effects of RBFOX1 are not yet understood. …
es, de, gb, us
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Jose Vicente Torres-Pérez, Adele Leggieri, Aleksandra M. Mech, Sofia Anagianni et autres
Abstract Williams syndrome (WS) is a multifaceted developmental disorder characterized by a spectrum of physical and intellectual traits. Individuals with WS exhibit friendly, impulsive, and hyper-social behaviours, often coupled with anxiety. WS is attributed to a microdeletion on chromosome 7q11.23, affecting several …
es, gb
(code pays fourni par la source)
2023
conference-abstract
OpenAlex
Xian Wang, Oliver Haworth, Adele Leggieri, Márta Korbonits et autres
Aryl hydrocarbon receptor-interacting protein (AIP) is a highly expressed, evolutionary conserved little-known co-chaperone molecule that can bind to client proteins. Heterozygous loss-of-function mutations of AIP are associated with pituitary adenomas. Multiple lines of evidence suggest that AIP has important functions beyond the …