Anuradha Dhingra, Meisheng Jiang, Tian-Li Wang, Arkady Lyubarsky, Andrey Savchenko, Tehilla Bar-Yehuda, Peter Sterling, Lutz Birnbaumer, Noga Vardi. J Neurosci 2002
Times Cited: 93
Times Cited: 93
Times Cited
Times Co-cited
Similarity
The light response of ON bipolar neurons requires G[alpha]o.
A Dhingra, A Lyubarsky, M Jiang, E N Pugh, L Birnbaumer, P Sterling, N Vardi. J Neurosci 2000
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Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
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The metabotropic receptor mGluR6 may signal through G(o), but not phosphodiesterase, in retinal bipolar cells.
S Nawy. J Neurosci 1999
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A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells.
Yin Shen, J Alexander Heimel, Maarten Kamermans, Neal S Peachey, Ronald G Gregg, Scott Nawy. J Neurosci 2009
Yin Shen, J Alexander Heimel, Maarten Kamermans, Neal S Peachey, Ronald G Gregg, Scott Nawy. J Neurosci 2009
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TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
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TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells.
Catherine W Morgans, Jianmei Zhang, Brett G Jeffrey, Steve M Nelson, Neal S Burke, Robert M Duvoisin, R Lane Brown. Proc Natl Acad Sci U S A 2009
Catherine W Morgans, Jianmei Zhang, Brett G Jeffrey, Steve M Nelson, Neal S Burke, Robert M Duvoisin, R Lane Brown. Proc Natl Acad Sci U S A 2009
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Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells.
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Gbeta5 is required for normal light responses and morphology of retinal ON-bipolar cells.
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A retinal-specific regulator of G-protein signaling interacts with Galpha(o) and accelerates an expressed metabotropic glutamate receptor 6 cascade.
Anuradha Dhingra, Eva Faurobert, Nathan Dascal, Peter Sterling, Noga Vardi. J Neurosci 2004
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Gbeta5-RGS complexes co-localize with mGluR6 in retinal ON-bipolar cells.
Catherine W Morgans, Theodore G Wensel, R Lane Brown, Jorge A Perez-Leon, Ben Bearnot, Robert M Duvoisin. Eur J Neurosci 2007
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Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
Maria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, Ralph J Florijn, Jillian N Pearring, Francoise M Meire, Maureen A McCall, Frans C C Riemslag, Ronald G Gregg, Arthur A B Bergen,[...]. Am J Hum Genet 2009
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TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Susanne Kohl, Bart P Leroy, Francis L Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F Nandrot, Birgit Lorenz, Markus Preising,[...]. Am J Hum Genet 2009
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Glutamate receptors of rod bipolar cells are linked to a cyclic GMP cascade via a G-protein.
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Localization of mGluR6 to dendrites of ON bipolar cells in primate retina.
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Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate.
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Suppression by glutamate of cGMP-activated conductance in retinal bipolar cells.
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Gβ3 is required for normal light ON responses and synaptic maintenance.
Anuradha Dhingra, Hariharasubramanian Ramakrishnan, Adam Neinstein, Marie E Fina, Ying Xu, Jian Li, Daniel C Chung, Arkady Lyubarsky, Noga Vardi. J Neurosci 2012
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Alpha subunit of Go localizes in the dendritic tips of ON bipolar cells.
N Vardi. J Comp Neurol 1998
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Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).
Rebecca R Bellone, Samantha A Brooks, Lynne Sandmeyer, Barbara A Murphy, George Forsyth, Sheila Archer, Ernest Bailey, Bruce Grahn. Genetics 2008
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Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.
Zheng Li, Panagiotis I Sergouniotis, Michel Michaelides, Donna S Mackay, Genevieve A Wright, Sophie Devery, Anthony T Moore, Graham E Holder, Anthony G Robson, Andrew R Webster. Am J Hum Genet 2009
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Retina-specific GTPase accelerator RGS11/G beta 5S/R9AP is a constitutive heterotrimer selectively targeted to mGluR6 in ON-bipolar neurons.
Yan Cao, Ikuo Masuho, Haruhisa Okawa, Keqiang Xie, Junko Asami, Paul J Kammermeier, Dennis M Maddox, Takahisa Furukawa, Takayoshi Inoue, Alapakkam P Sampath,[...]. J Neurosci 2009
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25
A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites.
Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
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ON cone bipolar cells in rat express the metabotropic receptor mGluR6.
N Vardi, K Morigiwa. Vis Neurosci 1997
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Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
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TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
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Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
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Congenital stationary night blindness with negative electroretinogram. A new classification.
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2-amino-4-phosphonobutyric acid: a new pharmacological tool for retina research.
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16
Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
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Multiple neurological abnormalities in mice deficient in the G protein Go.
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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
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L-glutamate-induced responses and cGMP-activated channels in three subtypes of retinal bipolar cells dissociated from the cat.
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Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
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TRPM1: the endpoint of the mGluR6 signal transduction cascade in retinal ON-bipolar cells.
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TRPM1 forms complexes with nyctalopin in vivo and accumulates in postsynaptic compartment of ON-bipolar neurons in mGluR6-dependent manner.
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A naturally occurring mouse model of X-linked congenital stationary night blindness.
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Identification of a G-protein in depolarizing rod bipolar cells.
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G protein subunit G gamma 13 is coexpressed with G alpha o, G beta 3, and G beta 4 in retinal ON bipolar cells.
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Coordinated control of sensitivity by two splice variants of Gα(o) in retinal ON bipolar cells.
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Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
Sherry L Ball, Patricia A Powers, Hee-Sup Shin, Catherine W Morgans, Neal S Peachey, Ronald G Gregg. Invest Ophthalmol Vis Sci 2002
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Instability of GGL domain-containing RGS proteins in mice lacking the G protein beta-subunit Gbeta5.
Ching-Kang Chen, Pamela Eversole-Cire, Haikun Zhang, Valeria Mancino, Yu-Jiun Chen, Wei He, Theodore G Wensel, Melvin I Simon. Proc Natl Acad Sci U S A 2003
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RGS7 and -11 complexes accelerate the ON-bipolar cell light response.
Jianmei Zhang, Brett G Jeffrey, Catherine W Morgans, Neal S Burke, Tammie L Haley, Robert M Duvoisin, R Lane Brown. Invest Ophthalmol Vis Sci 2010
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mGluR6 deletion renders the TRPM1 channel in retina inactive.
Ying Xu, Anuradha Dhingra, Marie E Fina, Chieko Koike, Takahisa Furukawa, Noga Vardi. J Neurophysiol 2012
Ying Xu, Anuradha Dhingra, Marie E Fina, Chieko Koike, Takahisa Furukawa, Noga Vardi. J Neurophysiol 2012
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G-protein-mediated inhibition of the Trp channel TRPM1 requires the Gβγ dimer.
Yin Shen, Melissa Ann F Rampino, Reed C Carroll, Scott Nawy. Proc Natl Acad Sci U S A 2012
Yin Shen, Melissa Ann F Rampino, Reed C Carroll, Scott Nawy. Proc Natl Acad Sci U S A 2012
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GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Neal S Peachey, Thomas A Ray, Ralph Florijn, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012
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12
11
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
N T Bech-Hansen, M J Naylor, T A Maybaum, W G Pearce, B Koop, G A Fishman, M Mets, M A Musarella, K M Boycott. Nat Genet 1998
11
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.