DNA methylation and regulation of gene expression: Guardian of our health
GA Dhar, S Saha, P Mitra, R Nag Chaudhuri - The Nucleus, 2021 - Springer
One of the most critical epigenetic signatures present in the genome of higher eukaryotes is
the methylation of DNA at the C-5 position of the cytosine ring. Based on the sites of DNA …
the methylation of DNA at the C-5 position of the cytosine ring. Based on the sites of DNA …
Blood-brain barrier regulation in psychiatric disorders
The blood-brain barrier (BBB) is a dynamic interface between the peripheral blood supply
and the cerebral parenchyma, controlling the transport of material to and from the brain …
and the cerebral parenchyma, controlling the transport of material to and from the brain …
Rescue of oxytocin response and social behaviour in a mouse model of autism
A fundamental challenge in develo** treatments for autism spectrum disorders is the
heterogeneity of the condition. More than one hundred genetic mutations confer high risk for …
heterogeneity of the condition. More than one hundred genetic mutations confer high risk for …
MMP‐9 in translation: from molecule to brain physiology, pathology, and therapy
Abstract Matrix metalloproteinase‐9 (MMP‐9) is a member of the metzincin family of mostly
extracellularly operating proteases. Despite the fact that all of these enzymes might be target …
extracellularly operating proteases. Despite the fact that all of these enzymes might be target …
The neuropathology of autism: A systematic review of post-mortem studies of autism and related disorders
Post-mortem studies allow for the direct investigation of brain tissue in those with autism and
related disorders. Several review articles have focused on aspects of post-mortem …
related disorders. Several review articles have focused on aspects of post-mortem …
MMPs in learning and memory and neuropsychiatric disorders
Matrix metalloproteinases (MMPs) are a group of over twenty proteases, operating chiefly
extracellularly to cleave components of the extracellular matrix, cell adhesion molecules as …
extracellularly to cleave components of the extracellular matrix, cell adhesion molecules as …
Fragile X syndrome
RJ Hagerman, E Berry-Kravis, HC Hazlett… - Nature reviews Disease …, 2017 - nature.com
Fragile X syndrome (FXS) is the leading inherited form of intellectual disability and autism
spectrum disorder, and patients can present with severe behavioural alterations, including …
spectrum disorder, and patients can present with severe behavioural alterations, including …
Dysregulation and restoration of translational homeostasis in fragile X syndrome
Fragile X syndrome (FXS), the most-frequently inherited form of intellectual disability and the
most-prevalent single-gene cause of autism, results from a lack of fragile X mental …
most-prevalent single-gene cause of autism, results from a lack of fragile X mental …
Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials
E Berry-Kravis, V Des Portes, R Hagerman… - Science translational …, 2016 - science.org
Fragile X syndrome (FXS), the most common cause of inherited intellectual disability and
autistic spectrum disorder, is typically caused by transcriptional silencing of the X-linked …
autistic spectrum disorder, is typically caused by transcriptional silencing of the X-linked …
Metformin ameliorates core deficits in a mouse model of fragile X syndrome
Fragile X syndrome (FXS) is the leading monogenic cause of autism spectrum disorders
(ASD). Trinucleotide repeat expansions in FMR1 abolish FMRP expression, leading to …
(ASD). Trinucleotide repeat expansions in FMR1 abolish FMRP expression, leading to …