Related references
Note: Only part of the references are listed.Zebrafish Models of Photoreceptor Dysfunction and Degeneration
Nicole C. L. Noel et al.
BIOMOLECULES (2021)
Development and characterization of a chronic photoreceptor degeneration model in adult zebrafish that does not trigger a regenerative response
Brooke Turkalj et al.
EXPERIMENTAL EYE RESEARCH (2021)
PHENOTYPIC CHARACTERISTICS OF ROD-CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
Samer Khateb et al.
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES (2020)
Transmembrane protein western blotting: Impact of sample preparation on detection of SLC11A2 (DMT1) and SLC40A1 (ferroportin)
Yoshiaki Tsuji
PLOS ONE (2020)
A Zebrafish Model of Retinitis Pigmentosa Shows Continuous Degeneration and Regeneration of Rod Photoreceptors
Abirami Santhanam et al.
CELLS (2020)
Elasticity of individual protocadherin 15 molecules implicates tip links as the gating springs for hearing
Tobias F. Bartsch et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)
Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration
Zhaojing Lu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2019)
A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies
Kaitlyn R. Calabro et al.
FRONTIERS IN NEUROSCIENCE (2019)
Beyond Cell-Cell Adhesion: Sensational Cadherins for Hearing and Balance
Avinash Jaiganesh et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2018)
Usherin defects lead to early-onset retinal dysfunction in zebrafish
Margo Dona et al.
EXPERIMENTAL EYE RESEARCH (2018)
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome
Didier Dulon et al.
JOURNAL OF CLINICAL INVESTIGATION (2018)
Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments
Alix Trouillet et al.
SCIENTIFIC REPORTS (2018)
TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells
Bifeng Pan et al.
NEURON (2018)
Mechanotransduction by PCDH15 Relies on a Novel cis-Dimeric Architecture
Gilman Dionne et al.
NEURON (2018)
Characterisation of maturation of photoreceptor cell subtypes during zebrafish retinal development
Catia Crespo et al.
BIOLOGY OPEN (2018)
High-throughput sequencing for the molecular diagnosis of Usher syndrome reveals 42 novel mutations and consolidates CEP250 as Usher-like disease causative
Carla Fuster-Garcia et al.
SCIENTIFIC REPORTS (2018)
Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment
Cataldo Schietroma et al.
JOURNAL OF CELL BIOLOGY (2017)
Integrin α8 and Pcdh15 act as a complex to regulate cilia biogenesis in sensory cells
Linda Goodman et al.
JOURNAL OF CELL SCIENCE (2017)
Functional Analysis of the Transmembrane and Cytoplasmic Domains of Pcdh15a in Zebrafish Hair Cells
Reo Maeda et al.
JOURNAL OF NEUROSCIENCE (2017)
Photoreceptor Cilia and Retinal Ciliopathies
Kinga M. Bujakowska et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2017)
Retina regeneration in zebrafish
Jin Wan et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2016)
Molecular basis for photoreceptor outer segment architecture
Andrew F. X. Goldberg et al.
PROGRESS IN RETINAL AND EYE RESEARCH (2016)
G9a and ZNF644 Physically Associate to Suppress Progenitor Gene Expression during Neurogenesis
Jonathan B. Olsen et al.
STEM CELL REPORTS (2016)
Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities
Pranav Mathur et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2015)
Rod disc renewal occurs by evagination of the ciliary plasma membrane that makes cadherin-based contacts with the inner segment
Thomas Burgoyne et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Spontaneous Regeneration of Human Photoreceptor Outer Segments
Jonathan C. Horton et al.
SCIENTIFIC REPORTS (2015)
Myosin VIIA is a Marker for the Cone Accessory Outer Segment in Zebrafish
Corinne Hodel et al.
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY (2014)
The retinal phenotype of Usher syndrome: Pathophysiological insights from animal models
Aziz El-Amraoui et al.
COMPTES RENDUS BIOLOGIES (2014)
Regulation of synaptic development and function by the Drosophila PDZ protein Dyschronic
James E. C. Jepson et al.
DEVELOPMENT (2014)
myosin 7aa-/- mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses
Meagan M. Wasfy et al.
EXPERIMENTAL EYE RESEARCH (2014)
Zebrafish Cacna1fa is required for cone photoreceptor function and synaptic ribbon formation
Sujuan Jia et al.
HUMAN MOLECULAR GENETICS (2014)
Usher protein functions in hair cells and photoreceptors
Dominic Cosgrove et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2014)
Clarin-1 acts as a modulator of mechanotransduction activity and presynaptic ribbon assembly
Oluwatobi Ogun et al.
JOURNAL OF CELL BIOLOGY (2014)
Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2
Reo Maeda et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice
Iman Sahly et al.
JOURNAL OF CELL BIOLOGY (2012)
Role for a Novel Usher Protein Complex in Hair Cell Synaptic Maturation
Marisa Zallocchi et al.
PLOS ONE (2012)
Ultrastructure of the distal retina of the adult zebrafish, Danio rerio
R. Tarboush et al.
TISSUE & CELL (2012)
Generation of a genetically encoded marker of rod photoreceptor outer segment growth and renewal
John J. Willoughby et al.
BIOLOGY OPEN (2012)
Harmonin (Ush1c) is required in zebrafish Muller glial cells for photoreceptor synaptic development and function
Jennifer B. Phillips et al.
DISEASE MODELS & MECHANISMS (2011)
Lateral Mobility of Presynaptic L-Type Calcium Channels at Photoreceptor Ribbon Synapses
Aaron J. Mercer et al.
JOURNAL OF NEUROSCIENCE (2011)
Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells
Kumar N. Alagramam et al.
PLOS ONE (2011)
Moderate Light-Induced Degeneration of Rod Photoreceptors with Delayed Transducin Translocation in shaker1 Mice
You-Wei Peng et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
Deafness and Retinal Degeneration in a Novel USH1C Knock-In Mouse Model
Jennifer J. Lentz et al.
DEVELOPMENTAL NEUROBIOLOGY (2010)
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
E. Ostergaard et al.
JOURNAL OF MEDICAL GENETICS (2010)
Structure of the N terminus of cadherin 23 reveals a new adhesion mechanism for a subset of cadherin superfamily members
Heather M. Elledge et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Association of Whirlin with Cav1.3 (α1D) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network
Ferry F. J. Kersten et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Early defects in photoreceptor outer segment morphogenesis in zebrafish ift57, ift88 and ift172 Intraflagellar Transport mutants
Sujita Sukumaran et al.
VISION RESEARCH (2009)
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice (vol 118, pg 2908, 2008)
Zhenglin Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Harmonin in the Murine Retina and the Retinal Phenotypes of Ush1c-Mutant Mice and Human USH1C
David S. Williams et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome
Zubair M. Ahmed et al.
HUMAN GENETICS (2008)
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Zhenglin Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells
Piotr Kazmierczak et al.
NATURE (2007)
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%
A-F Roux et al.
JOURNAL OF MEDICAL GENETICS (2006)
Molecular basis of human Usher syndrome:: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
Jan Reiners et al.
EXPERIMENTAL EYE RESEARCH (2006)
Ames waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts
Ricky J. L. Haywood-Watson et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
The retinal pigment epithelium in visual function
O Strauss
PHYSIOLOGICAL REVIEWS (2005)
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
XM Ouyang et al.
HUMAN GENETICS (2005)
Duplicated genes with split functions:: independent roles of protocadherin15 orthologues in zebraf ish hearing and vision
C Seiler et al.
DEVELOPMENT (2005)
Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells
J Reiners et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2003)
Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration
RT Libby et al.
EXPERIMENTAL EYE RESEARCH (2003)
A photoreceptor-specific cadherin is essential for the structural integrity of the outer segment and for photoreceptor survival
A Rattner et al.
NEURON (2001)
Synapse formation is arrested in retinal photoreceptors of the zebrafish nrc mutant
BA Allwardt et al.
JOURNAL OF NEUROSCIENCE (2001)