Höfundar: Katrin Möller

Þriðjudagur, 15. október

Málstofa: Molecular Biology

Loss of epigenetic machinery components causes neuronal DNA methylation abnormalities

Salur: AB1

Mánudagur, 14. október

Málstofa: Neural development

A strategy to identify functionally relevant DNA methylation abnormalities in neurons

Salur: I

Mánudagur, 14. október

Málstofa: Neural development

A systematic CRISPR-screen targeting EM-genes to uncover shared transcriptional dysregulations during neurodevelopment

Salur: I

Þriðjudagur, 15. október

Málstofa: Biomedical Sciences Genetics Multidisciplinary research

Differentiation rate affects DNA methylation abnormalities in neurons with epigenetic machinery knockout

Salur: AB1

Mánudagur, 14. október

Málstofa: Neural development

A systematic CRISPR-screen targeting EM-genes to uncover shared transcriptional dysregulations during neurodevelopment

Salur: I

Mánudagur, 14. október

Málstofa: Neural development

A strategy to identify functionally relevant DNA methylation abnormalities in neurons

Salur: I

Málstofa: Hópur B

Elucidating functionally important CpG sites in Neurodevelopmental Disorders via systematic knockout of EM genes

Salur: I

Málstofa: Genetics

Systematic disruption of EM genes to understand transcriptional effect and role in neurodevelopmental disorders.

Salur: B

Málstofa: Genetics and diseases

A mechanistic hypothesis explaining the occurrence of two distinct phenotypes from the CREBBP/EP300 genes

Salur: B

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