Jennifer N. Jahncke

This study shows that Dystroglycan's extracellular and intracellular domains have distinct roles in inhibitory synapse formation and maintenance in cerebellar Purkinje cells.

The paper evaluates Cre lines and a viral approach for conditional deletion in cerebellar Purkinje cells, showing variability in recombination efficiency and protein loss timing.

This study examines inhibitory synapse defects and seizure susceptibility in mouse models of dystroglycanopathy, showing that severe forms exhibit impaired CCK+/CB1R+ interneuron development and synaptic function.

This study examines the functional effects of two patient-specific Tbr1 mutations on cortical development in mice, revealing both shared and distinct phenotypes.

This study identifies molecular mechanisms downstream of non-ionotropic NMDA receptor signaling that drive dendritic spine shrinkage and LTD in hippocampal neurons.