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Topic: non-coding RNAs

Seminar
3 seminars

In Molecular Neuroscience and Developmental Neuroscience

Seminar · Epigenetics

Integration of „environmental“ information in the neuronal epigenome

Geraldine Zimmer-Bensch · Functional Epigenetics in the Animal Model, Institute of Biology II, RWTH Aachen, Aachen, Germany

Wed, Aug 25, 2021 · 16:00 UTC

The inhibitory actions of the heterogeneous collection of GABAergic interneurons tremendously influence cortical information processing, which is reflected by diseases like autism, epilepsy and schizophrenia that involve defects in cortical inhibition. Apart from the regulation of physiological processes like synaptic transmission, proper interneuron function also relies on their correct development. Hence, decrypting regulatory networks that direct proper cortical interneuron development as well as adult functionality is of great interest, as this helps to identify critical events implicated

Seminar · Epigenetics

From epigenetics to stratified therapies in neuropsychiatric diseases

Andre Fischer · University Medical Center Goettingen, DZNE Goettingen

Thu, Jun 17, 2021 · 16:45 UTC

The establishment of effective therapies for neurodegenerative and neuropsychiatric diseases is still challenging and one of the reasons is that especially for age-associated neurodegenerative diseases pathology accumulates long before there are any clinical signs of disease. Thus, patients are often only diagnosed at an already advanced state of molecular pathology, when causative therapies fail. Thus, there is an urgent need for molecular biomarkers that could detect individuals at risk for developing a CNS disease and stratify patients. I will address epigenetic processes such as histone-mo

Seminar · Molecular Biology

Translational upregulation of STXBP1 by non-coding RNAs as an innovative treatment for STXBP1 encephalopathy

Federico Zara & Ganna Balagura · Institute G. Gaslini, University of Genoa

Wed, Mar 17, 2021 · 16:00 UTC

Developmental and epileptic encephalopathies (DEEs) are a broad spectrum of genetic epilepsies associated with impaired neurological development as a direct consequence of a genetic mutation, in addition to the effect of the frequent epileptic activity on brain. Compelling genetic studies indicate that heterozygous de novo mutations represent the most common underlying genetic mechanism, in accordance with the sporadic presentation of DEE. De novo mutations may exert a loss-of-function (LOF) on the protein by decrementing expression level and/or activity, leading to functional haploinsufficien