Developmental social communication deficits in the Shank3 rat model of phelan‐mcdermid syndrome and autism spectrum disorder
EL Berg, NA Copping, JK Rivera, MC Pride… - Autism …, 2018 - Wiley Online Library
Mutations in the SHANK3 gene have been discovered in autism spectrum disorder (ASD),
and the intellectual disability, Phelan‐McDermid Syndrome. This study leveraged a new rat …
and the intellectual disability, Phelan‐McDermid Syndrome. This study leveraged a new rat …
Touchscreen learning deficits and normal social approach behavior in the Shank3B model of Phelan–McDermid syndrome and autism
SHANK3 is a synaptic scaffolding protein localized in the postsynaptic density and has a
crucial role in synaptogenesis and neural physiology. Deletions and point mutations in …
crucial role in synaptogenesis and neural physiology. Deletions and point mutations in …
The effects of chronic exposure to ambient traffic-related air pollution on Alzheimer's disease phenotypes in wildtype and genetically predisposed male and female …
…, AE Valenzuela, C Wallis, EL Berg… - Environmental …, 2021 - ehp.niehs.nih.gov
Background: Epidemiological data link traffic-related air pollution (TRAP) to increased risk
of Alzheimer’s disease (AD). Preclinical data corroborating this association are largely from …
of Alzheimer’s disease (AD). Preclinical data corroborating this association are largely from …
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11. 2-q13. 3 duplication syndrome
…, D Zolkowska, MC Pride, EL Berg… - Human molecular …, 2017 - academic.oup.com
Maternally derived copy number gains of human chromosome 15q11.2-q13.3 (Dup15q
syndrome or Dup15q) cause intellectual disability, epilepsy, developmental delay, hypotonia, …
syndrome or Dup15q) cause intellectual disability, epilepsy, developmental delay, hypotonia, …
Early lysosome defects precede neurodegeneration with amyloid-β and tau aggregation in NHE6-null rat brain
Loss-of-function mutations in the X-linked endosomal Na + /H + exchanger 6 (NHE6) cause
Christianson syndrome in males. Christianson syndrome involves endosome dysfunction …
Christianson syndrome in males. Christianson syndrome involves endosome dysfunction …
Generation of a Novel Rat Model of Angelman Syndrome with a Complete Ube3a Gene Deletion
Angelman syndrome (AS) is a rare genetic disorder characterized by severe intellectual
disability, seizures, lack of speech, and ataxia. The gene responsible for AS was identified as …
disability, seizures, lack of speech, and ataxia. The gene responsible for AS was identified as …
[HTML][HTML] Translational outcomes relevant to neurodevelopmental disorders following early life exposure of rats to chlorpyrifos
EL Berg, TM Ching, DA Bruun, JK Rivera… - Journal of …, 2020 - Springer
Background Neurodevelopmental disorders (NDDs), including intellectual disability, attention
deficit hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), are pervasive, …
deficit hyperactivity disorder (ADHD), and autism spectrum disorder (ASD), are pervasive, …
[HTML][HTML] Excessive laughter-like vocalizations, microcephaly, and translational outcomes in the Ube3a deletion rat model of Angelman syndrome
Angelman syndrome (AS) is a rare genetic neurodevelopmental disorder characterized by
intellectual disabilities, motor and balance deficits, impaired communication, and a happy, …
intellectual disabilities, motor and balance deficits, impaired communication, and a happy, …
[HTML][HTML] Developmental exposure to near roadway pollution produces behavioral phenotypes relevant to neurodevelopmental disorders in juvenile rats
EL Berg, LR Pedersen, MC Pride, SP Petkova… - Translational …, 2020 - nature.com
Epidemiological studies consistently implicate traffic-related air pollution (TRAP) and/or
proximity to heavily trafficked roads as risk factors for developmental delays and …
proximity to heavily trafficked roads as risk factors for developmental delays and …
Gait as a quantitative translational outcome measure in Angelman syndrome
Angelman syndrome (AS) is a genetic neurodevelopmental disorder characterized by
developmental delay, lack of speech, seizures, intellectual disability, hypotonia, and motor …
developmental delay, lack of speech, seizures, intellectual disability, hypotonia, and motor …