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Molecular Vision|January 14, 2014
Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouseJasmin Balmer, Rui Ji, Thomas A Ray, et al.
The Journal of Biological Chemistry|November 1, 2002
Gamma 1 subunit interactions within the skeletal muscle L-type voltage-gated calcium channelsJyothi Arikkath, Chien-Chang Chen, Christopher Ahern, et al.
Evolution; International Journal of Organic Evolution|July 5, 2012
Proteomic and UTR analyses of a rapidly evolving hypervariable family of vertebrate pheromonesDamien B Wilburn, Kathleen E Bowen, Ronald G Gregg, et al.
Investigative Ophthalmology & Visual Science|December 31, 2002
Identification of the gene and the mutation responsible for the mouse nob phenotypeRonald G Gregg, Suparna Mukhopadhyay, Sophie I Candille, et al.
Eneuro|January 22, 2020
LRIT3 is Required for Nyctalopin Expression and Normal ON and OFF Pathway Signaling in the RetinaNazarul Hasan, Gobinda Pangeni, Thomas A Ray, et al.
Neuron|April 25, 2006
Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activityJay Demas, Botir T Sagdullaev, Erick Green, et al.
Anesthesiology|July 28, 2004
Anesthetic requirement is increased in redheadsEdwin B Liem, Chun-Ming Lin, Mohammad-Irfan Suleman, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinismJennifer L Thomas, Thomas S Vihtelic, Aaron D denDekker, et al.
Experimental Eye Research|July 5, 2011
Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eyeTaylor R Murphy, Thomas S Vihtelic, Kristina E Ile, et al.
Plos One|November 10, 2010
Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylationYuanquan Song, Jason R Willer, Paul C Scherer, et al.
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