Cargando…

Loss of ASD-Related Molecule Cntnap2 Affects Colonic Motility in Mice

Mostrar otras versiones (1)

Gastrointestinal (GI) symptoms are highly prevalent among individuals with autism spectrum disorder (ASD), but the molecular link between ASD and GI dysfunction remains poorly understood. The enteric nervous system (ENS) is critical for normal GI motility and has been shown to be altered in mouse mo...

Descripción completa

Detalles Bibliográficos
Autores principales:	Robinson, Beatriz G., Oster, Beau A., Robertson, Keiramarie, Kaltschmidt, Julia A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cold Spring Harbor Laboratory 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153124/ https://www.ncbi.nlm.nih.gov/pubmed/37131706 http://dx.doi.org/10.1101/2023.04.17.537221

Ejemplares similares

Loss of ASD-related molecule Cntnap2 affects colonic motility in mice
por: Robinson, Beatriz G., et al.
Publicado: (2023)

CNTNAP2: exploring association with autism phenotypes in mice
Publicado: (2011)

CNTNAP2 variants affect early language development in the general population
por: Whitehouse, A J O, et al.
Publicado: (2011)

Differential impacts of Cntnap2 heterozygosity and Cntnap2 null homozygosity on axon and myelinated fiber development in mouse
por: Cifuentes-Diaz, Carmen, et al.
Publicado: (2023)

Defining the Contribution of CNTNAP2 to Autism Susceptibility
por: Sampath, Srirangan, et al.
Publicado: (2013)

Developmental Disruption of GABA(A)R-Meditated Inhibition in Cntnap2 KO Mice
por: Bridi, Morgan S., et al.
Publicado: (2017)

Lactobacillus reuteri normalizes altered fear memory in male Cntnap4 knockout mice
por: Zhang, Wenlong, et al.
Publicado: (2022)

Single-cell multiome sequencing clarifies enteric glial diversity and identifies an intraganglionic population poised for neurogenesis
por: Guyer, Richard A., et al.
Publicado: (2023)

Correction: Defining the Contribution of CNTNAP2 to Autism Susceptibility
por: Sampath, Srirangan, et al.
Publicado: (2013)

Association of GDNF and CNTNAP2 gene variants with gambling
por: Das, Arundhuti, et al.
Publicado: (2019)

Mutations of CNTNAP1 led to defects in neuronal development
por: Li, Wanxing, et al.
Publicado: (2020)

PTPRD and CNTNAP2 as markers of tumor aggressiveness in oligodendrogliomas
por: Rautajoki, Kirsi J., et al.
Publicado: (2022)

CNTNAP4 signaling regulates osteosarcoma disease progression
por: Qin, Qizhi, et al.
Publicado: (2023)

CNTNAP2 stabilizes interneuron dendritic arbors through CASK
por: Gao, Ruoqi, et al.
Publicado: (2018)

Suppression of Akt-mTOR pathway rescued the social behavior in Cntnap2-deficient mice
por: Xing, Xiaoliang, et al.
Publicado: (2019)

Evaluation of CNTNAP2 gene polymorphisms for exfoliation syndrome in Japanese
por: Shimizu, Ai, et al.
Publicado: (2012)

CNTNAP2 and Language Processing in Healthy Individuals as Measured with ERPs
por: Kos, Miriam, et al.
Publicado: (2012)

CNTNAP4 deficiency in dopaminergic neurons initiates parkinsonian phenotypes
por: Zhang, Wenlong, et al.
Publicado: (2020)

Degraded tactile coding in the Cntnap2 mouse model of autism
por: Wang, Han Chin, et al.
Publicado: (2023)

Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder
por: Gandhi, Tanya, et al.
Publicado: (2023)

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
por: Gregor, Anne, et al.
Publicado: (2011)

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis
por: Hengel, Holger, et al.
Publicado: (2017)

Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variants
por: Scala, Marcello, et al.
Publicado: (2021)

Spontaneous enteric nervous system activity precedes maturation of gastrointestinal motility
por: Dershowitz, Lori B., et al.
Publicado: (2023)

Altered Cerebellar Response to Somatosensory Stimuli in the Cntnap2 Mouse Model of Autism
por: Fernández, Marta, et al.
Publicado: (2021)

A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy
por: Letko, Anna, et al.
Publicado: (2020)

Immature Neurons and Radial Glia, But Not Astrocytes or Microglia, Are Altered in Adult Cntnap2 and Shank3 Mice, Models of Autism
por: Cope, Elise C., et al.
Publicado: (2016)

Cntnap4/Caspr4 Differentially Contributes to GABAergic and Dopaminergic Synaptic Transmission
por: Karayannis, T., et al.
Publicado: (2014)

CNTNAP3 Associated ATG16L1 Expression and Crohn's Disease
por: Qiao, Yu Qi, et al.
Publicado: (2015)

Dysregulation of Parvalbumin Expression in the Cntnap2−/− Mouse Model of Autism Spectrum Disorder
por: Lauber, Emanuel, et al.
Publicado: (2018)

CNTNAP1 Mutations and Their Clinical Presentations: New Case Report and Systematic Review
por: Sabbagh, Sandra, et al.
Publicado: (2020)

Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings
por: Mittal, Rea, et al.
Publicado: (2021)

Microglial targeted therapy relieves cognitive impairment caused by Cntnap4 deficiency
por: Zhang, Wenlong, et al.
Publicado: (2023)

Mitochondrial disorders and ASD. Mechanisms of mitochondrial dysfunction in ASD
por: Sidenkova, A.
Publicado: (2023)

Melatonin treatment of repetitive behavioral deficits in the Cntnap2 mouse model of autism spectrum disorder
por: Wang, Huei Bin, et al.
Publicado: (2020)

Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
por: Memis, Idil, et al.
Publicado: (2022)

A Novel CNTNAP2 Mutation Results in Abnormal Neuronal E/I Balance
por: Lu, Ping, et al.
Publicado: (2021)

Intermittent hypoxia-induced enhancement of sociability and working memory associates with CNTNAP2 upregulation
por: Zhang, Qing, et al.
Publicado: (2023)

Developmental changes in electrophysiological properties of auditory cortical neurons in the Cntnap2 knockout rat
por: Mann, Rajkamalpreet S., et al.
Publicado: (2023)

The Na(v)1.9 channel regulates colonic motility in mice
por: Copel, Carine, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_6j2900s5tbjmpqqplejrbd936t