Ongoing support of The Cognitive Neurophysiology Laboratory is provided through a grant from the Sheryl and Daniel R. Tishman Charitable FDA approved Drug Library chemical structure Foundation. All authors declare no conflict of interest, financial or otherwise, that would have impacted the work reported in this document. Abbreviations AD analog to digital ADI Autism Diagnostic Interview ADOS Autism Diagnostic Observation Scale ASD autism spectrum disorder

MUSIC multiple signal classification pSTS posterior superior temporal sulcus SBRI ‘Stereotyped Behaviors and Restricted Interests’ SNR signal-to-noise ratio TD typically developing VEP visual evoked potential VESPA visual evoked spread spectrum analysis WASI Wechsler Abbreviated Scale of Intelligence “
“Prenatal alcohol exposure (PAE) can produce a myriad of deficits. Unfortunately, affected individuals may also be exposed to the stress of an adverse home environment,

contributing to deficits of attentional processes that are the hallmark of optimal executive function. Male offspring of ad-libitum-fed Control (Con), Pairfed (PF), and PAE dams were randomly assigned to either a 5-day period of variable chronic MK-1775 manufacturer mild stress (CMS) or no CMS in adolescence. In adulthood, rats were trained in a non-match to sample task (T-maze), followed by extensive assessment in the five-choice serial reaction time task. Once rats acquired the five-choice serial reaction time task (stable accuracy), they were tested in three challenge conditions: (i) increased sustained attention, (ii) selective attention and, (iii) varying doses of d-amphetamine, an indirect dopamine and norepinephrine agonist. At birth and throughout the study, PAE offspring showed reduced Casein kinase 1 body weight. Moreover, although PAE animals were similar to Con animals

in task acquisition, they were progressively less proficient with transitions to shorter stimulus durations (decreased accuracy and increased omissions). Five days of adolescent CMS increased basal corticosterone levels in adolescence and disrupted cognitive performance in adulthood. Further, CMS augmented PAE-related disturbances in acquisition and, to a lesser extent, also disrupted attentional processes in Con and PF animals. Following task acquisition, challenges unmasked persistent attentional difficulties resulting from both PAE and adolescent CMS. In conclusion, PAE, adolescent CMS, and their interaction produced unique behavioural profiles that suggest vulnerability in select neurobiological processes at different stages of development. “
“The tumor suppressor protein p53 (Trp53) and the cell cycle inhibitor p27 Kip1 (Cdknb1) have both been implicated in regulating proliferation of adult subventricular zone (aSVZ) cells.