Cargando…
Setd5 haploinsufficiency alters neuronal network connectivity and leads to autistic-like behaviors in mice
SETD5, a gene linked to intellectual disability (ID) and autism spectrum disorder (ASD), is a member of the SET-domain family and encodes a putative histone methyltransferase (HMT). To date, the mechanism by which SETD5 haploinsufficiency causes ASD/ID remains an unanswered question. Setd5 is the hi...
Autores principales: | Moore, Spencer M., Seidman, Jason S., Ellegood, Jacob, Gao, Richard, Savchenko, Alex, Troutman, Ty D., Abe, Yohei, Stender, Josh, Lee, Daehoon, Wang, Sicong, Voytek, Bradley, Lerch, Jason P., Suh, Hoonkyo, Glass, Christopher K, Muotri, Alysson R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336863/ https://www.ncbi.nlm.nih.gov/pubmed/30655503 http://dx.doi.org/10.1038/s41398-018-0344-y |
Ejemplares similares
-
Pten haploinsufficiency causes desynchronized growth of brain areas involved in sensory processing
por: Clipperton-Allen, Amy E., et al.
Publicado: (2022) -
SETD5 haploinsufficiency affects mitochondrial compartment in neural cells
por: Zaghi, Mattia, et al.
Publicado: (2023) -
Pten haploinsufficiency disrupts scaling across brain areas during development in mice
por: Clipperton-Allen, Amy E., et al.
Publicado: (2019) -
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
por: Crippa, Milena, et al.
Publicado: (2020) -
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling
por: Amar, Megha, et al.
Publicado: (2021)