Genomic regulation of transcription and RNA processing by the multitasking Integrator complex

SA Welsh, A Gardini - Nature Reviews Molecular Cell Biology, 2023 - nature.com
In higher eukaryotes, fine-tuned activation of protein-coding genes and many non-coding
RNAs pivots around the regulated activity of RNA polymerase II (Pol II). The Integrator …

Fox transcription factors: from development to disease

ML Golson, KH Kaestner - Development, 2016 - journals.biologists.com
Forkhead box (Fox) transcription factors are evolutionarily conserved in organisms ranging
from yeast to humans. They regulate diverse biological processes both during development …

The genetic and molecular basis of developmental language disorder: A review

HS Mountford, R Braden, DF Newbury, AT Morgan - Children, 2022 - mdpi.com
Language disorders are highly heritable and are influenced by complex interactions
between genetic and environmental factors. Despite more than twenty years of research, we …

[PDF][PDF] O uso do canabidiol no tratamento da epilepsia

RLA MATOS, LA Spinola, LL Barboza… - Revista Virtual de …, 2017 - static.sites.sbq.org.br
O objetivo deste estudo consiste em reunir dados bibliográficos que descrevam o perfil
terapêutico do canabidiol (CBD), o principal componente não psicoativo da planta …

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

C Bacon, M Schneider, C Le Magueresse… - Molecular …, 2015 - nature.com
Neurodevelopmental disorders are multi-faceted and can lead to intellectual disability,
autism spectrum disorder and language impairment. Mutations in the Forkhead box FOXP1 …

Decoding the genetics of speech and language

SA Graham, SE Fisher - Current opinion in neurobiology, 2013 - Elsevier
Researchers are beginning to uncover the neurogenetic pathways that underlie our
unparalleled capacity for spoken language. Initial clues come from identification of genetic …

A Foxp2 mutation implicated in human speech deficits alters sequencing of ultrasonic vocalizations in adult male mice

J Chabout, A Sarkar, SR Patel, T Radden… - Frontiers in behavioral …, 2016 - frontiersin.org
Development of proficient spoken language skills is disrupted by mutations of the FOXP2
transcription factor. A heterozygous missense mutation in the KE family causes speech …

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

L Liu, J Lei, SJ Sanders, AJ Willsey, Y Kou, AE Cicek… - Molecular autism, 2014 - Springer
Background De novo loss-of-function (dnLoF) mutations are found twofold more often in
autism spectrum disorder (ASD) probands than their unaffected siblings. Multiple …

A chromosome-level reference genome and pangenome for barn swallow population genomics

S Secomandi, GR Gallo, M Sozzoni, A Iannucci… - Cell reports, 2023 - cell.com
Insights into the evolution of non-model organisms are limited by the lack of reference
genomes of high accuracy, completeness, and contiguity. Here, we present a chromosome …

Genomic influences on self-reported childhood maltreatment

S Dalvie, AX Maihofer, JRI Coleman, B Bradley… - Translational …, 2020 - nature.com
Childhood maltreatment is highly prevalent and serves as a risk factor for mental and
physical disorders. Self-reported childhood maltreatment appears heritable, but the specific …