A citation-based method for searching scientific literature

Franziska M Schneider, Florian Mohr, Marc Behrendt, Johannes Oberwinkler. Eur J Cell Biol 2015
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
200
53

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
194
53

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
156
53

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
142
46

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
366
38


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
52
38

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
153
38

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
123
38

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
30

TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function.
Chieko Koike, Tomohiro Numata, Hiroshi Ueda, Yasuo Mori, Takahisa Furukawa. Cell Calcium 2010
60
30

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
62
30

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
73
30

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
41
30

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
93
30

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
91
30

LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.
Marion Neuillé, Catherine W Morgans, Yan Cao, Elise Orhan, Christelle Michiels, José-Alain Sahel, Isabelle Audo, Robert M Duvoisin, Kirill A Martemyanov, Christina Zeitz. Eur J Neurosci 2015
26
30

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
23

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
36
23

Oligomeric state of purified transient receptor potential melastatin-1 (TRPM1), a protein essential for dim light vision.
Melina A Agosto, Zhixian Zhang, Feng He, Ivan A Anastassov, Sara J Wright, Jennifer McGehee, Theodore G Wensel. J Biol Chem 2014
13
23

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
104
23

Differential function of Gγ13 in rod bipolar and ON cone bipolar cells.
Hariharasubramanian Ramakrishnan, Anuradha Dhingra, Shanti R Tummala, Marie E Fina, Jian J Li, Arkady Lyubarsky, Noga Vardi. J Physiol 2015
11
27


Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
Mieke M C Bijveld, Ralph J Florijn, Arthur A B Bergen, L Ingeborgh van den Born, Maarten Kamermans, Liesbeth Prick, Frans C C Riemslag, Mary J van Schooneveld, Astrid M L Kappers, Maria M van Genderen. Ophthalmology 2013
54
23

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
88
23

ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
802
23

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
235
23

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
184
23

Retinal bipolar cells: elementary building blocks of vision.
Thomas Euler, Silke Haverkamp, Timm Schubert, Tom Baden. Nat Rev Neurosci 2014
192
23

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
97
23

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
124
23

The TRPM1 channel in ON-bipolar cells is gated by both the α and the βγ subunits of the G-protein Go.
Ying Xu, Cesare Orlandi, Yan Cao, Shengyan Yang, Chan-Il Choi, Vijayakanth Pagadala, Lutz Birnbaumer, Kirill A Martemyanov, Noga Vardi. Sci Rep 2016
20
23

Transient receptor potential melastatin 1 (TRPM1) is an ion-conducting plasma membrane channel inhibited by zinc ions.
Sachar Lambert, Anna Drews, Oleksandr Rizun, Thomas F J Wagner, Annette Lis, Stefanie Mannebach, Sandra Plant, Melanie Portz, Marcel Meissner, Stephan E Philipp,[...]. J Biol Chem 2011
51
23

Parallel processing in the mammalian retina.
Heinz Wässle. Nat Rev Neurosci 2004
668
23

Identification of molecular markers of bipolar cells in the murine retina.
Douglas S Kim, Sarah E Ross, Jeffrey M Trimarchi, John Aach, Michael E Greenberg, Constance L Cepko. J Comp Neurol 2008
88
23

Structure of the TRPA1 ion channel suggests regulatory mechanisms.
Candice E Paulsen, Jean-Paul Armache, Yuan Gao, Yifan Cheng, David Julius. Nature 2015
334
23

Structures of the calcium-activated, non-selective cation channel TRPM4.
Jiangtao Guo, Ji She, Weizhong Zeng, Qingfeng Chen, Xiao-Chen Bai, Youxing Jiang. Nature 2017
92
23

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
15



Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes.
Sulochana Devi, Yogananda Markandeya, Nityanand Maddodi, Anuradha Dhingra, Noga Vardi, Ravi C Balijepalli, Vijayasaradhi Setaluri. Pigment Cell Melanoma Res 2013
26
15


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
48
15

The role of Gbetagamma subunits in the organization, assembly, and function of GPCR signaling complexes.
Denis J Dupré, Mélanie Robitaille, R Victor Rebois, Terence E Hébert. Annu Rev Pharmacol Toxicol 2009
191
15

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
66
15


Retinal ON bipolar cells express a new PCP2 splice variant that accelerates the light response.
Ying Xu, Pyroja Sulaiman, Rod M Feddersen, Jian Liu, Robert G Smith, Noga Vardi. J Neurosci 2008
25
15

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, Mariana Wittmer, Ursula Forster, John Neidhardt, Bernd Wissinger, Eberhart Zrenner, Robert Wilke, Susanne Kohl,[...]. Am J Hum Genet 2006
105
15

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
346
15

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
367
15


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.