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BRITISH JOURNAL OF OPHTHALMOLOGY, ISSN 0007-1161, 03/2013, Volume 97, Issue 3, pp. 247 - 247
Journal Article
by Park, S and Li, CM and Ames, JB
BIOMOLECULAR NMR ASSIGNMENTS, ISSN 1874-2718, 10/2014, Volume 8, Issue 2, pp. 361 - 364
Calcium-binding protein 4 (CaBP4) regulates voltage-gated Ca2+ channels in retinal rod cells and specific mutations within CaBP4 are associated with congenital... 
BIOPHYSICS | Calcium | SPECTROSCOPY | CaBP4 | EF-hand | MUTATION | Retina | CaV1.4
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 2010, Volume 51, Issue 11, pp. 5943 - 5951
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 12/2016, Volume 57, Issue 15, pp. 6861 - 6869
Journal Article
Journal Article
Frontiers in Molecular Neuroscience, ISSN 1662-5099, 02/2012, Volume 5, Issue 2012
Photoreceptors, the light-sensitive receptor neurons of the retina, receive and transmit a plethora of visual informations from the surrounding world.... 
Ribbon synapse | CaBP4 | Photoreceptor | RIBEYE | 1.4 calcium channel | GCAP | Synaptic ribbon | EF-hands | ribbon synapse | CaV1.4 calcium channel | photoreceptor
Journal Article
Documenta Ophthalmologica, ISSN 0012-4486, 4/2018, Volume 136, Issue 2, pp. 135 - 143
CABP4-related retinal dysfunction is a cone–rod synaptic transmission disorder with electronegative electroretinogram (ERG) waveform. It is a rare retinal... 
Electroretinography | OCT | Medicine & Public Health | CABP4 | Hemeralopia | Multimodal fundus imaging | Ophthalmology | HIGH-HYPEROPIA | OPTICAL COHERENCE TOMOGRAPHY | PHENOTYPE | CLINICAL CHARACTERIZATION | POSTERIOR MICROPHTHALMOS | LEBER CONGENITAL AMAUROSIS | GENE | OPHTHALMOLOGY | MUTATIONS | STATIONARY NIGHT BLINDNESS | Retinal Diseases - genetics | Humans | Eye Diseases, Hereditary - diagnosis | Infant | Male | Myopia - diagnosis | Genetic Diseases, X-Linked - genetics | Retrospective Studies | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Fluorescein Angiography | European Continental Ancestry Group - genetics | France - epidemiology | Retinal Diseases - diagnosis | Eye Diseases, Hereditary - physiopathology | Night Blindness - diagnosis | Tomography, Optical Coherence - methods | Visual Acuity | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Myopia - genetics | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Mutation | Retinal Diseases - physiopathology | Fundus Oculi | Photoreceptor Cells, Vertebrate - pathology | Calcium-Binding Proteins - genetics | Medicine, Experimental | Medical research | Genetic disorders | Congenital diseases | Synaptic transmission | Blindness | Nystagmus | Tomography | Retina | Diagnosis | Nyctalopia | Stationary night blindness | Electroretinograms | Index Medicus
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 11/2007, Volume 27, Issue 46, pp. 12743 - 12754
CaBP4 is a calmodulin-like neuronal calcium-binding protein that is crucial for the development and/or maintenance of the cone and rod photoreceptor synapse.... 
Phosphorylation | CaBP4 | Protein kinase C ζ | channel | binding proteins | Photoreceptors | Ca | Ca2+-binding proteins | photoreceptors | protein kinase Cζ | phosphorylation | Ca2+ channel
Journal Article
Journal Article
Journal Article
Journal Article
Biomolecular NMR Assignments, ISSN 1874-2718, 10/2014, Volume 8, Issue 2, pp. 361 - 364
Calcium-binding protein 4 (CaBP4) regulates voltage-gated Ca2+ channels in retinal rod cells and specific mutations within CaBP4 are associated with congenital... 
Polymer Sciences | Biochemistry, general | Calcium | CaBP4 | EF-hand | Retina | Biophysics and Biological Physics | CaV1.4 | Physics | Genetic disorders | Binding proteins | Calmodulin | Protein binding | calcium | retina
Journal Article
FRONTIERS IN MOLECULAR NEUROSCIENCE, ISSN 1662-5099, 2012, Volume 5
Photoreceptors, the light-sensitive receptor neurons of the retina, receive and transmit a plethora of visual informations from the surrounding world.... 
CaBP4 | photoreceptor | RIBEYE | ribbon synapse | GCAP | synaptic ribbon | Ca(v)1.4 calcium channel | NEUROSCIENCES | EF-hands
Journal Article
CHANNELS, ISSN 1933-6950, 2013, Volume 7, Issue 6, pp. 514 - 523
Mutations in the gene encoding Ca(v)1.4, CACNA1F(,) are associated with visual disorders including X-linked incomplete congenital stationary night blindness... 
CACNA1F MUTATION | congenital stationary night blindness | Ca2+channel | CABP4 | BIOCHEMISTRY & MOLECULAR BIOLOGY | photoreceptor | CA2+ CHANNELS | RAT RETINA | ribbon synapse | CLINICAL VARIABILITY | CACNA1F | HAIR-CELLS | ROD PHOTORECEPTORS | CONE PHOTORECEPTORS | retina | LINKED RETINAL DISORDER | MOUSE RETINA | Cav1.4
Journal Article
JOURNAL OF NEUROSCIENCE, ISSN 0270-6474, 11/2007, Volume 27, Issue 46, pp. 12743 - 12754
Journal Article
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