Results 151 to 160 of about 2,216,286 (294)

Zebrafish in neurodevelopmental disorders studies: Genetic models and pathological involvement of microglia

open access: yesDevelopmental Medicine &Child Neurology, Volume 67, Issue 10, Page 1257-1265, October 2025.
The relevance of the pathogenic (de novo or inherited) mutations found in patients with neurodevelopmental disorders can be investigated using zebrafish as an animal model, by functional screening of the target genes and phenotypic assessments during both early development and adulthood. Abstract Neurodevelopmental disorders (NDDs) are a group of brain
Fatemeh Hassani Nia, Valerie Wittamer
wiley   +1 more source

Autism-associated SNPs in the clock genes _npas2_, _per1_ and the homeobox gene _en2_ alter DNA sequences that show characteristics of microRNA genes. [PDF]

open access: yes, 2008
Intronic single nucleotide polymorphisms (SNPs) in the clock genes _npas2_ and _per1_ and the homeobox gene _en2_ are reported to be associated with autism.
Brad Nicholas   +3 more
core   +1 more source

The Alternation of Gray Matter Morphological Topology in Drug-Naïve Tourette's Syndrome in Children. [PDF]

open access: yesFront Aging Neurosci, 2022
Liao Y   +10 more
europepmc   +1 more source

Cerebrospinal Fluid Biogenic Amines in Obsessive Compulsive Disorder, Tourette's Syndrome, and Healthy Controls [PDF]

open access: bronze, 1995
James F. Leckman   +11 more
openalex   +1 more source

Neurobiology of the Premonitory Urge in Tourette's Syndrome: Pathophysiology and Treatment Implications.

open access: yesThe Journal of Neuropsychiatry and Clinical Neurosciences, 2017
A. Cavanna   +3 more
semanticscholar   +1 more source

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