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 …
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 …
from yeast to humans. They regulate diverse biological processes both during development …
The genetic and molecular basis of developmental language disorder: A review
Language disorders are highly heritable and are influenced by complex interactions
between genetic and environmental factors. Despite more than twenty years of research, we …
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 …
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 …
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 …
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
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 …
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
Background De novo loss-of-function (dnLoF) mutations are found twofold more often in
autism spectrum disorder (ASD) probands than their unaffected siblings. Multiple …
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 …
genomes of high accuracy, completeness, and contiguity. Here, we present a chromosome …
Genomic influences on self-reported childhood maltreatment
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 …
physical disorders. Self-reported childhood maltreatment appears heritable, but the specific …