A citation-based method for searching scientific literature

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







List of co-cited articles
951 articles co-cited >1



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
158
69

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
369
46


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
154
35

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
199
33

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
203
29

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
356
27

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
80
32


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
56
37

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
146
22

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
161
22


Localization of mGluR6 to dendrites of ON bipolar cells in primate retina.
N Vardi, R Duvoisin, G Wu, P Sterling. J Comp Neurol 2000
147
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
42
42


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
106
18

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
125
18

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
67
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
64
26


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
167
17

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
61
26

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
237
16

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
351
16


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
71
21

Multiple neurological abnormalities in mice deficient in the G protein Go.
M Jiang, M S Gold, G Boulay, K Spicher, M Peyton, P Brabet, Y Srinivasan, U Rudolph, G Ellison, L Birnbaumer. Proc Natl Acad Sci U S A 1998
164
15


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
186
15


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
108
15

TRPM1: the endpoint of the mGluR6 signal transduction cascade in retinal ON-bipolar cells.
Catherine W Morgans, Ronald Lane Brown, Robert M Duvoisin. Bioessays 2010
68
20


A naturally occurring mouse model of X-linked congenital stationary night blindness.
M T Pardue, M A McCall, M M LaVail, R G Gregg, N S Peachey. Invest Ophthalmol Vis Sci 1998
127
13

Identification of a G-protein in depolarizing rod bipolar cells.
N Vardi, D F Matesic, D R Manning, P A Liebman, P Sterling. Vis Neurosci 1993
64
20

G protein subunit G gamma 13 is coexpressed with G alpha o, G beta 3, and G beta 4 in retinal ON bipolar cells.
Liquan Huang, Marianna Max, Robert F Margolskee, Hui Su, Richard H Masland, Thomas Euler. J Comp Neurol 2003
98
13

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
21
61


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
146
12

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
168
12

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
31
38

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
37
32

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
53
22

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
94
12

Immunocytochemical analysis of the mouse retina.
S Haverkamp, H Wässle. J Comp Neurol 2000
569
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
369
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.