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Publications by Laura Steenpass

Corrigendum: Angelman Syndrome-Derived Neurons Display Late Onset of Paternal UBE3A Silencing

Scientific Reports

Multidisciplinary

English

A Novel mtDNA Large-Scale Mutation Clinically Exclusively Presenting With Refractory Anemia

Journal of Pediatric Hematology/Oncology

English

Related publications

Mitochondrial Dysfunction in CA1 Hippocampal Neurons of the UBE3A Deficient Mouse Model for Angelman Syndrome

Neuroscience Letters

English

Mutation Analysis of UBE3A in Angelman Syndrome Patients

American Journal of Human Genetics

English

Proteomics Analysis of an UBE3A Knockout Mouse Modelling Angelman Syndrome

English

Tissue-Specific Variation of Ube3a Protein Expression in Rodents and in a Mouse Model of Angelman Syndrome

Neurobiology of Disease

English

Ube3a Loss Increases Excitability and Blunts Orientation Tuning in the Visual Cortex of Angelman Syndrome Model Mice

Journal of Neurophysiology

English

Subcellular Organization of UBE3A in Neurons

Journal of Comparative Neurology

English

Late-Onset Severe Long QT Syndrome

Annals of Noninvasive Electrocardiology

Cardiovascular Medicine

English

26. Protein Delivery of an Artificial Transcription Factor Restores Widespread Ube3a Expression in an Angelman Syndrome Mouse Brain

Molecular Therapy

Molecular Medicine

Molecular Biology

English

A Behavioral Test Battery for Mouse Models of Angelman Syndrome: A Powerful Tool for Testing Drugs and Novel Ube3a Mutants

Molecular Autism

Developmental Neuroscience

Developmental Biology

Molecular Biology

English