Zoekresultaten
21
jan
15:00
- 17:00
… database WikiPathways: www.wikipathways.org/instance/WP4657. The most striking observation of this pathway was that observed phenotypes can be caused or influenced not by one but multiple genes in this region, although TBX1 was thought to be mainly responsible for heart defects. Woosub Shin PhD candidate Department of Bioinformatics - BiGCaT, NUTRIM Title : Applying pathway interaction method to hypothesize molecular signature of neuropsychiatric diseases caused by 22q11.2 deletion … molecular pathways leading to shared effects on brain structure across pathogenic copy number variants. Abstract : Recent findings have revealed convergent effects of multiple CNVs on different chromosomes, on core sensory, cognitive, and motor domains. Furthermore, recent evidence showed that the penetrance of a CNV for schizophrenia and developmental delay – reflecting the probability of manifesting the given phenotype – was associated with changes in medial white matter structures. These …
03
mei
13:00
- 16:00
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