ype Elgersma

Affiliations: 
Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 
Area:
learning and memory
Google:
"ype Elgersma"
Mean distance: 14.27 (cluster 6)
 
SNBCP
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Rauen KA, Alsaegh A, Ben-Shachar S, et al. (2019) First International Conference on RASopathies and Neurofibromatoses in Asia: Identification and advances of new therapeutics. American Journal of Medical Genetics. Part A
Ferner RE, Bakker A, Elgersma Y, et al. (2019) From process to progress-2017 International Conference on Neurofibromatosis 1, Neurofibromatosis 2 and Schwannomatosis. American Journal of Medical Genetics. Part A
Sonzogni M, Wallaard I, Santos SS, et al. (2018) A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel mutants. Molecular Autism. 9: 47
Onori MP, Koopal B, Everman DB, et al. (2018) The intellectual disability-associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain-of-function. Human Mutation
Rotaru DC, van Woerden GM, Wallaard I, et al. (2018) Adult gene reinstatement restores the electrophysiological deficits of prefrontal cortex layer 5 neurons in a mouse model of Angelman syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Wang T, van Woerden GM, Elgersma Y, et al. (2017) Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome. Frontiers in Cellular Neuroscience. 11: 418
Bazzigaluppi P, Isenia SC, Haasdijk ED, et al. (2017) Modulation of Murine Olivary Connexin 36 Gap Junctions by PKA and CaMKII. Frontiers in Cellular Neuroscience. 11: 397
van der Wal L, Bezstarosti K, Sap KA, et al. (2017) Improvement of ubiquitylation site detection by Orbitrap mass spectrometry. Journal of Proteomics
Küry S, van Woerden GM, Besnard T, et al. (2017) De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. American Journal of Human Genetics. 101: 768-788
Wallace ML, van Woerden GM, Elgersma Y, et al. (2017) UBE3A loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice. Journal of Neurophysiology. jn.00618.2016
See more...