C Sakai, S Ijaz, EJ Hoffman - Frontiers in molecular neuroscience, 2018 - frontiersin.org
Zebrafish are increasingly being utilized as a model system to investigate the function of the growing list of risk genes associated with neurodevelopmental disorders. This is due in large …
HC Martin, GE Kim, AT Pagnamenta… - Human molecular …, 2014 - academic.oup.com
In severe early-onset epilepsy, precise clinical and molecular genetic diagnosis is complex, as many metabolic and electro-physiological processes have been implicated in disease …
Intellectual disability (ID) is a neurodevelopmental condition affecting 1–3% of the world's population. Genetic factors play a key role causing the congenital limitations in intellectual …
M Katoh, M Katoh - International journal of …, 2017 - … .spandidos-publications.com
Canonical WNT signaling through Frizzled and LRP5/6 receptors is transduced to the WNT/β-catenin and WNT/stabilization of proteins (STOP) signaling cascades to regulate cell …
Wnt signaling function starts during the development of the nervous system and is crucial for synaptic plasticity in the adult brain. Clearly Wnt effects in synaptic and plastic processes are …
HN Cukier, ND Dueker, SH Slifer, JM Lee… - Molecular autism, 2014 - Springer
Abstract Background Autism spectrum disorders (ASDs) comprise a range of neurodevelopmental conditions of varying severity, characterized by marked qualitative …
DM Romero, N Bahi-Buisson, F Francis - Seminars in cell & developmental …, 2018 - Elsevier
Cerebral cortical development involves a complex series of highly regulated steps to generate the laminated structure of the adult neocortex. Neuronal migration is a key part of …
S Balestrini, SM Sisodiya - Neuroscience letters, 2018 - Elsevier
There is high variability in the response to antiepileptic treatment across people with epilepsy. Genetic factors significantly contribute to such variability. Recent advances in the …
T Chen, M Giri, Z Xia, YN Subedi… - … disease and treatment, 2017 - Taylor & Francis
Epilepsy is a common episodic neurological disorder or condition characterized by recurrent epileptic seizures, and genetics seems to play a key role in its etiology. Early linkage studies …