Autism spectrum disorders: etiology and pathology
Autism spectrum disorders (ASD) are a group of neurodevelopmental diseases. The cause
of ASD is unknown, but several genetic and non-genetic risk factors have been�…
of ASD is unknown, but several genetic and non-genetic risk factors have been�…
[HTML][HTML] GABAergic system dysfunction in autism spectrum disorders
H Zhao, X Mao, C Zhu, X Zou, F Peng…�- Frontiers in cell and�…, 2022 - frontiersin.org
Autism spectrum disorder (ASD) refers to a series of neurodevelopmental diseases
characterized by two hallmark symptoms, social communication deficits and repetitive�…
characterized by two hallmark symptoms, social communication deficits and repetitive�…
[HTML][HTML] mTOR-related synaptic pathology causes autism spectrum disorder-associated functional hyperconnectivity
Postmortem studies have revealed increased density of excitatory synapses in the brains of
individuals with autism spectrum disorder (ASD), with a putative link to aberrant mTOR�…
individuals with autism spectrum disorder (ASD), with a putative link to aberrant mTOR�…
[HTML][HTML] Dendritic spines shape analysis—classification or clusterization? Perspective
E Pchitskaya, I Bezprozvanny�- Frontiers in synaptic neuroscience, 2020 - frontiersin.org
Dendritic spines are small protrusions from the dendrite membrane, where contact with
neighboring axons is formed in order to receive synaptic input. Changes in size, shape, and�…
neighboring axons is formed in order to receive synaptic input. Changes in size, shape, and�…
Spatial centrosome proteome of human neural cells uncovers disease-relevant heterogeneity
AC O'Neill, F Uzbas, G Antognolli, F Merino…�- Science, 2022 - science.org
The centrosome provides an intracellular anchor for the cytoskeleton, regulating cell
division, cell migration, and cilia formation. We used spatial proteomics to elucidate protein�…
division, cell migration, and cilia formation. We used spatial proteomics to elucidate protein�…
Cortical wiring by synapse type–specific control of local protein synthesis
Neurons use local protein synthesis to support their morphological complexity, which
requires independent control across multiple subcellular compartments up to the level of�…
requires independent control across multiple subcellular compartments up to the level of�…
mRNA transport, translation, and decay in adult mammalian central nervous system axons
Localized mRNA translation regulates synapse function and axon maintenance, but how
compartment-specific mRNA repertoires are regulated is largely unknown. We developed an�…
compartment-specific mRNA repertoires are regulated is largely unknown. We developed an�…
[HTML][HTML] Fragile X syndrome: from molecular aspect to clinical treatment
DD Protic, R Aishworiya, MJ Salcedo-Arellano…�- International journal of�…, 2022 - mdpi.com
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by the full mutation as
well as highly localized methylation of the fragile X mental retardation 1 (FMR1) gene on the�…
well as highly localized methylation of the fragile X mental retardation 1 (FMR1) gene on the�…
[HTML][HTML] Noteworthy perspectives on microglia in neuropsychiatric disorders
H Zhu, A Guan, J Liu, L Peng, Z Zhang…�- Journal of�…, 2023 - Springer
Microglia are so versatile that they not only provide immune surveillance for central nervous
system, but participate in neural circuitry development, brain blood vessels formation, blood�…
system, but participate in neural circuitry development, brain blood vessels formation, blood�…
Ythdf is a N6‐methyladenosine reader that modulates Fmr1 target mRNA selection and restricts axonal growth in Drosophila
L Worpenberg, C Paolantoni, S Longhi…�- The EMBO�…, 2021 - embopress.org
Abstract N6‐methyladenosine (m6A) regulates a variety of physiological processes through
modulation of RNA metabolism. This modification is particularly enriched in the nervous�…
modulation of RNA metabolism. This modification is particularly enriched in the nervous�…