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Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.
The Science of the Total Environment|January 31, 2012
Graveyards - special landfillsS Fiedler, J Breuer, C M Pusch, et al.
The Journal of General Physiology|July 4, 2001
Mechanism of block of single protopores of the Torpedo chloride channel ClC-0 by 2-(p-chlorophenoxy)butyric acid (CPB)M Pusch, A Accardi, A Liantonio, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Genetic heterogeneity of deafness phenotypes linked to DFNA4Tao Yang, Markus Pfister, Nikolaus Blin, et al.
Human Genetics|September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1F K Jacobi, M Broghammer, K Pesch, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2001
Intracellular calcium dependence of large dense-core vesicle exocytosis in the absence of synaptotagmin IT Voets, T Moser, P E Lund, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 1, 1997
Alteration of Ca2+ dependence of neurotransmitter release by disruption of Ca2+ channel/syntaxin interactionJ Rettig, C Heinemann, U Ashery, et al.
Neuron|August 11, 1998
Munc13-1 is a presynaptic phorbol ester receptor that enhances neurotransmitter releaseA Betz, U Ashery, M Rickmann, et al.
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