Results 141 to 150 of about 44,093 (262)

Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.

open access: yesInvestigative Ophthalmology and Visual Science, 2005
C. Zeitz   +12 more
semanticscholar   +1 more source

mGluR6 deletion renders the TRPM1 channel in retina inactive.

open access: yesJournal of Neurophysiology, 2012
Ying Xu   +5 more
semanticscholar   +1 more source

Sleep Deprivation in Rats Causes Dissociation of the Synaptic NMDA Receptor/D1 Dopamine Receptor Heterocomplex. [PDF]

open access: yesNeuroSci
Kiknadze N   +8 more
europepmc   +1 more source

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses

open access: yesJournal of Physiology, 2008
D. Maddox   +19 more
semanticscholar   +1 more source

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