Catherine W Morgans, Ronald Lane Brown, Robert M Duvoisin. Bioessays 2010
Times Cited: 68
Times Cited: 68
Times Cited
Times Co-cited
Similarity
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
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
54
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
51
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
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
42
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
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
39
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
36
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
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
33
Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
M Masu, H Iwakabe, Y Tagawa, T Miyoshi, M Yamashita, Y Fukuda, H Sasaki, K Hiroi, Y Nakamura, R Shigemoto. Cell 1995
M Masu, H Iwakabe, Y Tagawa, T Miyoshi, M Yamashita, Y Fukuda, H Sasaki, K Hiroi, Y Nakamura, R Shigemoto. Cell 1995
30
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
Thaddeus P Dryja, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan. Proc Natl Acad Sci U S A 2005
Thaddeus P Dryja, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan. Proc Natl Acad Sci U S A 2005
27
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
A Dhingra, A Lyubarsky, M Jiang, E N Pugh, L Birnbaumer, P Sterling, N Vardi. J Neurosci 2000
25
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
Rebecca R Bellone, Samantha A Brooks, Lynne Sandmeyer, Barbara A Murphy, George Forsyth, Sheila Archer, Ernest Bailey, Bruce Grahn. Genetics 2008
25
TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
27
TRPM1 forms complexes with nyctalopin in vivo and accumulates in postsynaptic compartment of ON-bipolar neurons in mGluR6-dependent manner.
Yan Cao, Ekaterina Posokhova, Kirill A Martemyanov. J Neurosci 2011
Yan Cao, Ekaterina Posokhova, Kirill A Martemyanov. J Neurosci 2011
28
Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F O Luhmann, Frank Hoeben, Ursula Forster, Katharina Wycisk, Gábor Mátyás, Carel B Hoyng, Frans Riemslag,[...]. Invest Ophthalmol Vis Sci 2005
Christina Zeitz, Maria van Genderen, John Neidhardt, Ulrich F O Luhmann, Frank Hoeben, Ursula Forster, Katharina Wycisk, Gábor Mátyás, Carel B Hoyng, Frans Riemslag,[...]. Invest Ophthalmol Vis Sci 2005
23
TRPM1 mutations are associated with the complete form of congenital stationary night blindness.
Makoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, Akishi Onishi, Koji M Nishiguchi, Chieko Koike, Mikiko Kadowaki, Mineo Kondo, Yozo Miyake, Takahisa Furukawa. Mol Vis 2010
Makoto Nakamura, Rikako Sanuki, Tetsuhiro R Yasuma, Akishi Onishi, Koji M Nishiguchi, Chieko Koike, Mikiko Kadowaki, Mineo Kondo, Yozo Miyake, Takahisa Furukawa. Mol Vis 2010
22
Light response of retinal ON bipolar cells requires a specific splice variant of Galpha(o).
Anuradha Dhingra, Meisheng Jiang, Tian-Li Wang, Arkady Lyubarsky, Andrey Savchenko, Tehilla Bar-Yehuda, Peter Sterling, Lutz Birnbaumer, Noga Vardi. J Neurosci 2002
Anuradha Dhingra, Meisheng Jiang, Tian-Li Wang, Arkady Lyubarsky, Andrey Savchenko, Tehilla Bar-Yehuda, Peter Sterling, Lutz Birnbaumer, Noga Vardi. J Neurosci 2002
20
TRPM1 forms ion channels associated with melanin content in melanocytes.
Elena Oancea, Joris Vriens, Sebastian Brauchi, Janice Jun, Igor Splawski, David E Clapham. Sci Signal 2009
Elena Oancea, Joris Vriens, Sebastian Brauchi, Janice Jun, Igor Splawski, David E Clapham. Sci Signal 2009
19
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
N T Bech-Hansen, M J Naylor, T A Maybaum, R L Sparkes, B Koop, D G Birch, A A Bergen, C F Prinsen, R C Polomeno, A Gal,[...]. Nat Genet 2000
17
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
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
17
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
Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
18
Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
Ronald G Gregg, Maarten Kamermans, Jan Klooster, Peter D Lukasiewicz, Neal S Peachey, Kirstan A Vessey, Maureen A McCall. J Neurophysiol 2007
Ronald G Gregg, Maarten Kamermans, Jan Klooster, Peter D Lukasiewicz, Neal S Peachey, Kirstan A Vessey, Maureen A McCall. J Neurophysiol 2007
16
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
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
35
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Isabelle Audo, Kinga Bujakowska, Elise Orhan, Charlotte M Poloschek, Sabine Defoort-Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D Luu, Odile Lecompte, Eberhart Zrenner,[...]. Am J Hum Genet 2012
Isabelle Audo, Kinga Bujakowska, Elise Orhan, Charlotte M Poloschek, Sabine Defoort-Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien D Luu, Odile Lecompte, Eberhart Zrenner,[...]. Am J Hum Genet 2012
16
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
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
16
Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells.
A Nomura, R Shigemoto, Y Nakamura, N Okamoto, N Mizuno, S Nakanishi. Cell 1994
A Nomura, R Shigemoto, Y Nakamura, N Okamoto, N Mizuno, S Nakanishi. Cell 1994
14
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers,[...]. Nat Genet 2000
14
Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction.
Mineo Kondo, Rikako Sanuki, Shinji Ueno, Yuji Nishizawa, Naozumi Hashimoto, Hiroshi Ohguro, Shuichi Yamamoto, Shigeki Machida, Hiroko Terasaki, Grazyna Adamus,[...]. PLoS One 2011
Mineo Kondo, Rikako Sanuki, Shinji Ueno, Yuji Nishizawa, Naozumi Hashimoto, Hiroshi Ohguro, Shuichi Yamamoto, Shigeki Machida, Hiroko Terasaki, Grazyna Adamus,[...]. PLoS One 2011
16
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.
Dennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, Brandon M Invergo, Donald R Cantrell, Samsoon Inayat, Victoria Balannik, Wanda L Hicks, Norman L Hawes, Shannon Byers,[...]. J Physiol 2008
Dennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, Brandon M Invergo, Donald R Cantrell, Samsoon Inayat, Victoria Balannik, Wanda L Hicks, Norman L Hawes, Shannon Byers,[...]. J Physiol 2008
18
The metabotropic receptor mGluR6 may signal through G(o), but not phosphodiesterase, in retinal bipolar cells.
S Nawy. J Neurosci 1999
S Nawy. J Neurosci 1999
13
Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate.
Y Nakajima, H Iwakabe, C Akazawa, H Nawa, R Shigemoto, N Mizuno, S Nakanishi. J Biol Chem 1993
Y Nakajima, H Iwakabe, C Akazawa, H Nawa, R Shigemoto, N Mizuno, S Nakanishi. J Biol Chem 1993
13
Gbeta5 is required for normal light responses and morphology of retinal ON-bipolar cells.
Anjali Rao, Rebecca Dallman, Scott Henderson, Ching-Kang Chen. J Neurosci 2007
Anjali Rao, Rebecca Dallman, Scott Henderson, Ching-Kang Chen. J Neurosci 2007
13
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
T M Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, B H Weber, K Wutz, N Gutwillinger, K Rüther, B Drescher,[...]. Nat Genet 1998
13
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
13
Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
13
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
16
Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells.
Anuradha Dhingra, Marie E Fina, Adam Neinstein, David J Ramsey, Ying Xu, Gerald A Fishman, Kenneth R Alexander, Haohua Qian, Neal S Peachey, Ronald G Gregg,[...]. J Neurosci 2011
Anuradha Dhingra, Marie E Fina, Adam Neinstein, David J Ramsey, Ying Xu, Gerald A Fishman, Kenneth R Alexander, Haohua Qian, Neal S Peachey, Ronald G Gregg,[...]. J Neurosci 2011
18
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013
13
GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes.
Cesare Orlandi, Ekaterina Posokhova, Ikuo Masuho, Thomas A Ray, Nazarul Hasan, Ronald G Gregg, Kirill A Martemyanov. J Cell Biol 2012
Cesare Orlandi, Ekaterina Posokhova, Ikuo Masuho, Thomas A Ray, Nazarul Hasan, Ronald G Gregg, Kirill A Martemyanov. J Cell Biol 2012
13
Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
Christina Zeitz, Anthony G Robson, Isabelle Audo. Prog Retin Eye Res 2015
Christina Zeitz, Anthony G Robson, Isabelle Audo. Prog Retin Eye Res 2015
13
Comparisons of structural and functional abnormalities in mouse b-wave mutants.
Maureen A McCall, Ronald G Gregg. J Physiol 2008
Maureen A McCall, Ronald G Gregg. J Physiol 2008
19
Synaptic transmission at retinal ribbon synapses.
Ruth Heidelberger, Wallace B Thoreson, Paul Witkovsky. Prog Retin Eye Res 2005
Ruth Heidelberger, Wallace B Thoreson, Paul Witkovsky. Prog Retin Eye Res 2005
11
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
Catherine W Morgans, Theodore G Wensel, R Lane Brown, Jorge A Perez-Leon, Ben Bearnot, Robert M Duvoisin. Eur J Neurosci 2007
14
Coordinated control of sensitivity by two splice variants of Gα(o) in retinal ON bipolar cells.
Haruhisa Okawa, Johan Pahlberg, Fred Rieke, Lutz Birnbaumer, Alapakkam P Sampath. J Gen Physiol 2010
Haruhisa Okawa, Johan Pahlberg, Fred Rieke, Lutz Birnbaumer, Alapakkam P Sampath. J Gen Physiol 2010
38
Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F Schorderet, Eberhart Zrenner,[...]. Am J Hum Genet 2006
Christina Zeitz, Barbara Kloeckener-Gruissem, Ursula Forster, Susanne Kohl, István Magyar, Bernd Wissinger, Gábor Mátyás, François-Xavier Borruat, Daniel F Schorderet, Eberhart Zrenner,[...]. Am J Hum Genet 2006
11
Two R7 regulator of G-protein signaling proteins shape retinal bipolar cell signaling.
Deb Kumar Mojumder, Yan Qian, Theodore G Wensel. J Neurosci 2009
Deb Kumar Mojumder, Yan Qian, Theodore G Wensel. J Neurosci 2009
19
Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
Katharina A Wycisk, Birgit Budde, Silke Feil, Sergej Skosyrski, Francesca Buzzi, John Neidhardt, Esther Glaus, Peter Nürnberg, Klaus Ruether, Wolfgang Berger. Invest Ophthalmol Vis Sci 2006
Katharina A Wycisk, Birgit Budde, Silke Feil, Sergej Skosyrski, Francesca Buzzi, John Neidhardt, Esther Glaus, Peter Nürnberg, Klaus Ruether, Wolfgang Berger. Invest Ophthalmol Vis Sci 2006
10
Defective retinal depolarizing bipolar cells in regulators of G protein signaling (RGS) 7 and 11 double null mice.
Hoon Shim, Chih-Ting Wang, Yen-Lin Chen, Viet Q Chau, Kevin G Fu, Jianqi Yang, A Rory McQuiston, Rory A Fisher, Ching-Kang Chen. J Biol Chem 2012
Hoon Shim, Chih-Ting Wang, Yen-Lin Chen, Viet Q Chau, Kevin G Fu, Jianqi Yang, A Rory McQuiston, Rory A Fisher, Ching-Kang Chen. J Biol Chem 2012
21
Regulators of G protein signaling RGS7 and RGS11 determine the onset of the light response in ON bipolar neurons.
Yan Cao, Johan Pahlberg, Ignacio Sarria, Naomi Kamasawa, Alapakkam P Sampath, Kirill A Martemyanov. Proc Natl Acad Sci U S A 2012
Yan Cao, Johan Pahlberg, Ignacio Sarria, Naomi Kamasawa, Alapakkam P Sampath, Kirill A Martemyanov. Proc Natl Acad Sci U S A 2012
12
Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Neal S Peachey, Jillian N Pearring, Pasano Bojang, Matthew E Hirschtritt, Gwen Sturgill-Short, Thomas A Ray, Takahisa Furukawa, Chieko Koike, Andrew F X Goldberg, Yin Shen,[...]. J Neurophysiol 2012
Neal S Peachey, Jillian N Pearring, Pasano Bojang, Matthew E Hirschtritt, Gwen Sturgill-Short, Thomas A Ray, Takahisa Furukawa, Chieko Koike, Andrew F X Goldberg, Yin Shen,[...]. J Neurophysiol 2012
20
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
Anuradha Dhingra, Hariharasubramanian Ramakrishnan, Adam Neinstein, Marie E Fina, Ying Xu, Jian Li, Daniel C Chung, Arkady Lyubarsky, Noga Vardi. J Neurosci 2012
16
Clinical and immunologic characteristics of melanoma-associated retinopathy syndrome: eleven new cases and a review of 51 previously published cases.
J L Keltner, C E Thirkill, P T Yip. J Neuroophthalmol 2001
J L Keltner, C E Thirkill, P T Yip. J Neuroophthalmol 2001
8
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.