Development of a preclinical testing platform for clinically relevant therapy for Dravet syndrome
Abstract Objective Patients with drug‐resistant epilepsy, including Dravet syndrome, are frequently prescribed multiple antiseizure medications. Nevertheless, people with Dravet syndrome often have inadequate seizure control, and there is an ongoing unmet clinical need to identify novel therapeutics.
Jeffrey A. Mensah +7 more
wiley +1 more source
<i>GJB2</i> enhances cancer stem cell properties by modulating <i>SOX2</i> expression via NF-κB pathway activation in lung adenocarcinoma. [PDF]
You Q +6 more
europepmc +1 more source
Epigenetic control of cell identities from epiblast to gastrulation
In this review, we present and contextualize current knowledge about the roles of epigenetic modifiers during the development of mouse epiblast to gastrulation stage. The epigenetic regulation of enhancer and promoter elements by DNA methylation, histone modifications, and chromatin accessibility in concert with lineage‐specific transcription factors ...
Katrin M. Schüle, Simone Probst
wiley +1 more source
Silk fibroin hydrogel with recombinant silk fibroin/NT3 protein enhances wound healing by promoting type III collagen synthesis and hair follicle regeneration in skin injury. [PDF]
Yan Y +10 more
europepmc +1 more source
Neocortical neurogenesis: a proneural gene perspective
The neocortex is a mammalian‐specific brain region responsible for higher‐order cognitive functioning that shares fundamental similarities across species, but which is larger and more complex in humans. Proneural genes, encoding basic helix–loop–helix transcription factors (TFs), are evolutionarily conserved drivers of neurogenesis from fly to human ...
Lakshmy Vasan +3 more
wiley +1 more source
DSG3 promotes bladder cancer growth and metastasis via AKT/GSK3β/β-catenin pathway. [PDF]
Wang T +11 more
europepmc +1 more source
Gle1 knockout mice fail to segregate cell lineages at the blastocyst stage, resulting in very early embryonic lethality. Gle1 knock‐in (KI) mice harboring a pathogenic variant giving rise to lethal congenital contracture syndrome 1 show both known and novel innervation defects, supportive of multiorgan pathology in human fetuses.
Tomáš Zárybnický +22 more
wiley +1 more source
Phaeochromocytomas and paragangliomas harbour tumour-initiating SOX2+ stem cells
Kemkem Y +22 more
europepmc +1 more source
Pluripotency genes of mammals: a network at work. [PDF]
Cancedda R, Mastrogiacomo M.
europepmc +1 more source

