Cargando…

Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders

BACKGROUND: Motor deficits such as abnormal gait are an underappreciated yet characteristic phenotype of many neurodevelopmental disorders (NDDs), including Williams Syndrome (WS) and Neurofibromatosis Type 1 (NF1). Compared to cognitive phenotypes, gait phenotypes are readily and comparably assesse...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rahn, Rachel M., Weichselbaum, Claire T., Gutmann, David H., Dougherty, Joseph D., Maloney, Susan E.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980331/ https://www.ncbi.nlm.nih.gov/pubmed/33743598 http://dx.doi.org/10.1186/s11689-021-09359-0

Ejemplares similares

The trajectory of gait development in mice
por: Akula, Shyam K., et al.
Publicado: (2020)

DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders
por: Christian, Diana L., et al.
Publicado: (2020)

Shared mechanisms of neural circuit disruption in tuberous sclerosis across lifespan: Bridging neurodevelopmental and neurodegenerative pathology
por: Litwa, Karen
Publicado: (2022)

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
por: Cukier, Holly N, et al.
Publicado: (2014)

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
por: Rees, Elliott, et al.
Publicado: (2021)

Maternal Fluoxetine Exposure Alters Cortical Hemodynamic and Calcium Response of Offspring to Somatosensory Stimuli
por: Rahn, Rachel M., et al.
Publicado: (2019)

Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders
por: Yang, Yongjie, et al.
Publicado: (2013)

Editorial: Language across neurodevelopmental disorders
por: Filipe, Marisa G., et al.
Publicado: (2023)

Sleep Duration in Mouse Models of Neurodevelopmental Disorders
por: Saré, Rachel Michelle, et al.
Publicado: (2020)

Mapping a shared genetic basis for neurodevelopmental disorders
por: Jensen, Matthew, et al.
Publicado: (2017)

Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum
por: Yang, Zhiyu, et al.
Publicado: (2021)

A comprehensive assay of social motivation reveals sex-specific roles of autism-associated genes and oxytocin
por: Maloney, Susan E., et al.
Publicado: (2023)

Developmental pyrethroid exposure causes a neurodevelopmental disorder phenotype in mice
por: Curtis, Melissa A, et al.
Publicado: (2023)

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
por: Gillentine, Madelyn A., et al.
Publicado: (2021)

Developmental milestones in early childhood and genetic liability to neurodevelopmental disorders
por: Hannigan, Laurie J., et al.
Publicado: (2023)

Developmental hypomyelination in Wolfram syndrome: new insights from neuroimaging and gene expression analyses
por: Samara, Amjad, et al.
Publicado: (2019)

Developmental disruption and restoration of brain synaptome architecture in the murine Pax6 neurodevelopmental disease model
por: Tomas-Roca, Laura, et al.
Publicado: (2022)

Loss of Quaking RNA binding protein disrupts the expression of genes associated with astrocyte maturation in mouse brain
por: Sakers, Kristina, et al.
Publicado: (2021)

The spatiotemporal organization of episodic memory and its disruption in a neurodevelopmental disorder
por: Mastrogiuseppe, Marilina, et al.
Publicado: (2019)

Blood–Brain Barrier Disruption and Its Involvement in Neurodevelopmental and Neurodegenerative Disorders
por: Aragón-González, Ana, et al.
Publicado: (2022)

Visual Evoked Potential in Children With Developmental Disorders: Correlation With Neurodevelopmental Outcomes
por: Kim, JaYoung, et al.
Publicado: (2018)

The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
por: Mossink, Britt, et al.
Publicado: (2020)

MYT1L in the making: emerging insights on functions of a neurodevelopmental disorder gene
por: Chen, Jiayang, et al.
Publicado: (2022)

Developmental Language Disorder: Wake and Sleep Epileptiform Discharges and Co-morbid Neurodevelopmental Disorders
por: Dlouha, Olga, et al.
Publicado: (2020)

A trivalent nucleosome interaction by PHIP/BRWD2 is disrupted in neurodevelopmental disorders and cancer
por: Morgan, Marc A.J., et al.
Publicado: (2021)

Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure
por: Laufer, Benjamin I., et al.
Publicado: (2022)

Interrogating the mouse thalamus to correct human neurodevelopmental disorders
por: Schmitt, L. Ian, et al.
Publicado: (2016)

Inaugural annual special section of the intellectual and developmental disabilities research centers: developmental cognitive neuroscience and neurodevelopmental disorders
por: Jeste, Shafali Spurling, et al.
Publicado: (2018)

11th International Conference on Developmental Coordination Disorder (DCD11): Developmental coordination disorder and other neurodevelopmental disorders: a focus on comorbidity
Publicado: (2015)

Coordinated cortical thickness alterations across six neurodevelopmental and psychiatric disorders
por: Hettwer, M. D., et al.
Publicado: (2022)

The Locus Preservation Hypothesis: Shared Linguistic Profiles across Developmental Disorders and the Resilient Part of the Human Language Faculty
por: Leivada, Evelina, et al.
Publicado: (2017)

Neurodevelopmental disorders and cancer networks share pathways, but differ in mechanisms, signaling strength, and outcome
por: Yavuz, Bengi Ruken, et al.
Publicado: (2023)

Multigenerational metabolic disruption: Developmental origins and mechanisms of propagation across generations
por: Davis, Daniel D., et al.
Publicado: (2022)

Author Correction: The spatiotemporal organization of episodic memory and its disruption in a neurodevelopmental disorder
por: Mastrogiuseppe, Marilina, et al.
Publicado: (2020)

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders
por: Guo, Hui, et al.
Publicado: (2019)

Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders
por: Zhou, Jian, et al.
Publicado: (2022)

Investigating Gait, Movement, and Coordination in Children with Neurodevelopmental Disorders: Is There a Role for Motor Abnormalities in Atypical Neurodevelopment?
por: Colizzi, Marco, et al.
Publicado: (2020)

Distinct Basal Metabolism in Three Mouse Models of Neurodevelopmental Disorders
por: Menzies, Caitlin, et al.
Publicado: (2021)

Developmental pyrethroid exposure disrupts folate metabolism in mouse brain
por: Curtis, Melissa A., et al.
Publicado: (2023)

Visual deprivation during mouse critical period reorganizes network-level functional connectivity
por: Chen, Siyu, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_2qi4iiq33090qrerl7q64sfrum