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
Times Cited: 190
Times Cited: 190
Times Cited
Times Co-cited
Similarity
Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.
Françoise Haeseleer, Yoshikazu Imanishi, Tadao Maeda, Daniel E Possin, Akiko Maeda, Amy Lee, Fred Rieke, Krzysztof Palczewski. Nat Neurosci 2004
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The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
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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
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Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
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Calcium channel-dependent molecular maturation of photoreceptor synapses.
Nawal Zabouri, Silke Haverkamp. PLoS One 2013
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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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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
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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
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Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
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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
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Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
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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
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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
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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
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X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
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Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
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Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retina.
Philippa R Bayley, Catherine W Morgans. J Comp Neurol 2007
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The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.
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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).
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
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Congenital stationary night blindness with negative electroretinogram. A new classification.
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Localization of the alpha(1F) calcium channel subunit in the rat retina.
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The Auxiliary Calcium Channel Subunit α2δ4 Is Required for Axonal Elaboration, Synaptic Transmission, and Wiring of Rod Photoreceptors.
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Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina.
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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
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17
C-terminal modulator controls Ca2+-dependent gating of Ca(v)1.4 L-type Ca2+ channels.
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Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex.
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Switching off calcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain.
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The diverse roles of ribbon synapses in sensory neurotransmission.
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Photoreceptor calcium channels: insight from night blindness.
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Synaptic transmission at retinal ribbon synapses.
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Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation.
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Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.
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Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
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50
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
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RIBEYE, a component of synaptic ribbons: a protein's journey through evolution provides insight into synaptic ribbon function.
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14
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
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23
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.
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21
TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
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14
Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision.
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21
CaV1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype.
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16
Alternative splicing at C terminus of Ca(V)1.4 calcium channel modulates calcium-dependent inactivation, activation potential, and current density.
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Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.
Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi,[...]. Nat Neurosci 2008
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12
Early steps in the assembly of photoreceptor ribbon synapses in the mouse retina: the involvement of precursor spheres.
Hanna Regus-Leidig, Susanne Tom Dieck, Dana Specht, Lars Meyer, Johann Helmut Brandstätter. J Comp Neurol 2009
Hanna Regus-Leidig, Susanne Tom Dieck, Dana Specht, Lars Meyer, Johann Helmut Brandstätter. J Comp Neurol 2009
15
A novel CACNA1F gene mutation causes Aland Island eye disease.
Reetta Jalkanen, N Torben Bech-Hansen, Rose Tobias, Eeva-Marja Sankila, Maija Mäntyjärvi, Henrik Forsius, Albert de la Chapelle, Tiina Alitalo. Invest Ophthalmol Vis Sci 2007
Reetta Jalkanen, N Torben Bech-Hansen, Rose Tobias, Eeva-Marja Sankila, Maija Mäntyjärvi, Henrik Forsius, Albert de la Chapelle, Tiina Alitalo. Invest Ophthalmol Vis Sci 2007
31
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
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12
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
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
21
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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.