Search Results - "De Ruiter, Martijn"
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1
Voltage-Gated Sodium Channels in Cerebellar Purkinje Cells of Mormyrid Fish
Published in Journal of neurophysiology (01-07-2006)“…Department of Neuroscience, Erasmus University Medical Center, Rotterdam, The Netherlands Submitted 30 August 2005; accepted in final form 31 March 2006…”
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2
Exploring novel dilazep derivatives as hENT1 inhibitors and potentially covalent molecular tools
Published in Purinergic signalling (15-06-2024)“…The human equilibrative nucleoside transporter 1 (SLC29A1, hENT1) is a solute carrier that modulates the passive transport of nucleosides and nucleobases, such…”
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3
Hearing loss in infantile Pompe's disease and determination of underlying pathology in the knockout mouse
Published in Neurobiology of disease (01-06-2004)“…Hearing deficit occurs in several lysosomal storage disorders but has so far not been recognized as a symptom of Pompe's disease (glycogen storage disease type…”
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4
Alcohol Impairs Long-Term Depression at the Cerebellar Parallel Fiber-Purkinje Cell Synapse
Published in Journal of neurophysiology (01-12-2008)“…1 Department of Neuroscience, Erasmus University Medical Center, Rotterdam; 2 Netherlands Institute for Neuroscience, Royal Academy of Sciences, Amsterdam, The…”
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5
The Value-Add of Tailored Seasonal Forecast Information for Industry Decision Making
Published in Climate (Basel) (01-10-2022)“…There is a growing need for more systematic, robust, and comprehensive information on the value-add of climate services from both the demand and supply sides…”
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6
Otolith Deprivation Induces Optokinetic Compensation
Published in Journal of neurophysiology (01-11-2005)“…Department of Neuroscience, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands Submitted 11 February 2005; accepted in final form 27 July…”
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7
Hearing loss following Gata3 haploinsufficiency is caused by cochlear disorder
Published in Neurobiology of disease (01-06-2004)“…Patients with HDR syndrome suffer from hypoparathyroidism, deafness, and renal dysplasia due to a heterozygous deletion of the transcription factor GATA3…”
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