A citation-based method for searching scientific literature

Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda, Daniel E Possin, Akiko Maeda, Amy Lee, Fred Rieke, Krzysztof Palczewski. Nat Neurosci 2004
Times Cited: 218







List of co-cited articles
1513 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
Fiona Mansergh, Noelle C Orton, John P Vessey, Melanie R Lalonde, William K Stell, Francois Tremblay, Steven Barnes, Derrick E Rancourt, N Torben Bech-Hansen. Hum Mol Genet 2005
190
54

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
Bo Chang, John R Heckenlively, Philippa R Bayley, Nicholas C Brecha, Muriel T Davisson, Norm L Hawes, Arlene A Hirano, Ronald E Hurd, Akihiro Ikeda, Britt A Johnson,[...]. Vis Neurosci 2006
162
36

The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina.
Oliver Dick, Susanne tom Dieck, Wilko Detlef Altrock, Josef Ammermüller, Reto Weiler, Craig Curtis Garner, Eckart Dieter Gundelfinger, Johann Helmut Brandstätter. Neuron 2003
309
27

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
122
26

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
371
26

Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2.
Xiaoni Liu, Vasily Kerov, Françoise Haeseleer, Anurima Majumder, Nikolai Artemyev, Sheila A Baker, Amy Lee. Channels (Austin) 2013
66
37

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
347
24

Five members of a novel Ca(2+)-binding protein (CABP) subfamily with similarity to calmodulin.
F Haeseleer, I Sokal, C L Verlinde, H Erdjument-Bromage, P Tempst, A N Pronin, J L Benovic, R N Fariss, K Palczewski. J Biol Chem 2000
203
22

Complex regulation of voltage-dependent activation and inactivation properties of retinal voltage-gated Cav1.4 L-type Ca2+ channels by Ca2+-binding protein 4 (CaBP4).
Lior Shaltiel, Christos Paparizos, Stefanie Fenske, Sami Hassan, Christian Gruner, Katrin Rötzer, Martin Biel, Christian A Wahl-Schott. J Biol Chem 2012
33
66

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
91
24

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
21

A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
Karin W Littink, Maria M van Genderen, Rob W J Collin, Susanne Roosing, Arjan P M de Brouwer, Frans C C Riemslag, Hanka Venselaar, Alberta A H J Thiadens, Carel B Hoyng, Klaus Rohrschneider,[...]. Invest Ophthalmol Vis Sci 2009
57
33


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
18

Ca2+-binding proteins tune Ca2+-feedback to Cav1.3 channels in mouse auditory hair cells.
Guiying Cui, Alexander C Meyer, Irina Calin-Jageman, Jakob Neef, Françoise Haeseleer, Tobias Moser, Amy Lee. J Physiol 2007
80
22

Switching of Ca2+-dependent inactivation of Ca(v)1.3 channels by calcium binding proteins of auditory hair cells.
Philemon S Yang, Badr A Alseikhan, Hakim Hiel, Lisa Grant, Masayuki X Mori, Wanjun Yang, Paul A Fuchs, David T Yue. J Neurosci 2006
119
17


Deletion of the presynaptic scaffold CAST reduces active zone size in rod photoreceptors and impairs visual processing.
Susanne tom Dieck, Dana Specht, Nicola Strenzke, Yamato Hida, Vidhyasankar Krishnamoorthy, Karl-Friedrich Schmidt, Eiji Inoue, Hiroyoshi Ishizaki, Miki Tanaka-Okamoto, Jun Miyoshi,[...]. J Neurosci 2012
59
27

Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2.
Dagmar Knoflach, Vasily Kerov, Simone B Sartori, Gerald J Obermair, Claudia Schmuckermair, Xiaoni Liu, Vithiyanjali Sothilingam, Marina Garcia Garrido, Sheila A Baker, Martin Glösmann,[...]. Channels (Austin) 2013
39
41

Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology.
Mary A Raven, Noelle C Orton, Hadi Nassar, Gary A Williams, William K Stell, Gerald H Jacobs, N Torben Bech-Hansen, Benjamin E Reese. J Comp Neurol 2008
53
28

C-terminal modulator controls Ca2+-dependent gating of Ca(v)1.4 L-type Ca2+ channels.
Anamika Singh, Daniel Hamedinger, Jean-Charles Hoda, Mathias Gebhart, Alexandra Koschak, Christoph Romanin, Jörg Striessnig. Nat Neurosci 2006
97
15

A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.
Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar, Maria Magdalena Picher, Manou Sommen, Celia Zazo Seco, Jaap Oostrik, Hannie Kremer,[...]. Am J Hum Genet 2012
61
24

Allostery in Ca²⁺ channel modulation by calcium-binding proteins.
Philemon S Yang, Manu Ben Johny, David T Yue. Nat Chem Biol 2014
37
40

Characterization of Cav1.4 complexes (α11.4, β2, and α2δ4) in HEK293T cells and in the retina.
Amy Lee, Shiyi Wang, Brittany Williams, Jussara Hagen, Todd E Scheetz, Françoise Haeseleer. J Biol Chem 2015
37
40


Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex.
Susanne tom Dieck, Wilko D Altrock, Michael M Kessels, Britta Qualmann, Hanna Regus, Dana Brauner, Anna Fejtová, Oliver Bracko, Eckart D Gundelfinger, Johann H Brandstätter. J Cell Biol 2005
299
14

Congenital stationary night blindness with negative electroretinogram. A new classification.
Y Miyake, K Yagasaki, M Horiguchi, Y Kawase, T Kanda. Arch Ophthalmol 1986
352
14


Structural and functional remodeling in the retina of a mouse with a photoreceptor synaptopathy: plasticity in the rod and degeneration in the cone system.
Dana Specht, Susanne Tom Dieck, Josef Ammermüller, Hanna Regus-Leidig, Eckart Dieter Gundelfinger, Johann Helmut Brandstätter. Eur J Neurosci 2007
54
25

Switching off calcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain.
Christian Wahl-Schott, Ludwig Baumann, Hartmut Cuny, Christian Eckert, Kristina Griessmeier, Martin Biel. Proc Natl Acad Sci U S A 2006
62
22

The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.
John E McRory, Jawed Hamid, Clinton J Doering, Esperanza Garcia, Robin Parker, Kevin Hamming, Lina Chen, Michael Hildebrand, Aaron M Beedle, Laura Feldcamp,[...]. J Neurosci 2004
146
14

Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
Hanna Regus-Leidig, Jenny Atorf, Andreas Feigenspan, Jan Kremers, Marion A Maw, Johann Helmut Brandstätter. PLoS One 2014
40
35

Synaptogenesis in the photoreceptor terminal of the mouse retina.
J C Blanks, A M Adinolfi, R N Lolley. J Comp Neurol 1974
182
13




Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
Dana Specht, Shu-Biao Wu, Paul Turner, Peter Dearden, Frank Koentgen, Uwe Wolfrum, Marion Maw, Johann Helmut Brandstätter, Susanne tom Dieck. Invest Ophthalmol Vis Sci 2009
77
16

The Auxiliary Calcium Channel Subunit α2δ4 Is Required for Axonal Elaboration, Synaptic Transmission, and Wiring of Rod Photoreceptors.
Yuchen Wang, Katherine E Fehlhaber, Ignacio Sarria, Yan Cao, Norianne T Ingram, Debbie Guerrero-Given, Ben Throesch, Kristin Baldwin, Naomi Kamasawa, Toshihisa Ohtsuka,[...]. Neuron 2017
55
23

Differential modulation of Ca(v)2.1 channels by calmodulin and Ca2+-binding protein 1.
Amy Lee, Ruth E Westenbroek, Françoise Haeseleer, Krzysztof Palczewski, Todd Scheuer, William A Catterall. Nat Neurosci 2002
151
12

Ca2+-binding protein-1 facilitates and forms a postsynaptic complex with Cav1.2 (L-type) Ca2+ channels.
Hong Zhou, Seong-Ah Kim, Elizabeth A Kirk, Alyssa L Tippens, Hong Sun, Françoise Haeseleer, Amy Lee. J Neurosci 2004
85
14

A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype.
Mohammed A Aldahmesh, Mohammed Al-Owain, Faisal Alqahtani, Salwa Hazzaa, Fowzan S Alkuraya. Mol Vis 2010
29
37

Structure and function of ribbon synapses.
Peter Sterling, Gary Matthews. Trends Neurosci 2005
218
11

Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina.
Ryota L Matsuoka, Zheng Jiang, Ivy S Samuels, Kim T Nguyen-Ba-Charvet, Lu O Sun, Neal S Peachey, Alain Chédotal, King-Wai Yau, Alex L Kolodkin. J Neurosci 2012
51
21

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
11

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
200
11

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
R Jalkanen, M Mäntyjärvi, R Tobias, J Isosomppi, E-M Sankila, T Alitalo, N T Bech-Hansen. J Med Genet 2006
58
18

The diverse roles of ribbon synapses in sensory neurotransmission.
Gary Matthews, Paul Fuchs. Nat Rev Neurosci 2010
193
11

Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1.2 L-type Ca2+ channels by calmodulin and Ca2+-binding protein 1.
Shimrit Oz, Adva Benmocha, Yehezkel Sasson, Dana Sachyani, Lior Almagor, Amy Lee, Joel A Hirsch, Nathan Dascal. J Biol Chem 2013
29
37

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
J Platzer, J Engel, A Schrott-Fischer, K Stephan, S Bova, H Chen, H Zheng, J Striessnig. Cell 2000
624
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.