Cargando…

Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal Vasculature

PURPOSE: Familial exudative vitreoretinopathy (FEVR) is an inherited retinal disease in which the retinal vasculature is affected. Patients with FEVR typically lack or have abnormal vasculature in the peripheral retina, the outcome of which can range from mild visual impairment to complete blindness...

Descripción completa

Detalles Bibliográficos
Autores principales:	Karjosukarso, Dyah W., Ali, Zaheer, Peters, Theo A., Zhang, Jia Qi Cheng, Hoogendoorn, Anita D M., Garanto, Alejandro, van Wijk, Erwin, Jensen, Lasse D., Collin, Rob W J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Association for Research in Vision and Ophthalmology 2020
Materias:	Biochemistry and Molecular Biology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329629/ https://www.ncbi.nlm.nih.gov/pubmed/32097476 http://dx.doi.org/10.1167/iovs.61.2.39

Ejemplares similares

Mutation spectrum of the FZD-4, TSPAN12 AND ZNF408 genes in Indian FEVR patients
por: Musada, Ganeswara Rao, et al.
Publicado: (2016)

FEVR-Like Presentation of Homocystinuria
por: Montalvo, Lorena A., et al.
Publicado: (2014)

Dr. Egbert Le Fevre
Publicado: (1914)

Genetic and clinical characteristics of ZNF408-related familial exudative vitreoretinopathy
por: Tao, Xueying, et al.
Publicado: (2023)

The zinc finger proteins ZNF644 and WIZ regulate the G9a/GLP complex for gene repression
por: Bian, Chunjing, et al.
Publicado: (2015)

Correction: The zinc finger proteins ZNF644 and WIZ regulate the G9a/GLP complex for gene repression
por: Bian, Chunjing, et al.
Publicado: (2015)

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish
por: Messchaert, Muriël, et al.
Publicado: (2018)

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish
por: Corral-Serrano, Julio C., et al.
Publicado: (2018)

A Survey of Multigenic Protein-Altering Variant Frequency in Familial Exudative Vitreo-Retinopathy (FEVR) Patients by Targeted Sequencing of Seven FEVR-Linked Genes
por: Cicerone, Amanda Petrelli, et al.
Publicado: (2022)

Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for EYS-Associated Retinitis Pigmentosa
por: Schellens, Renske, et al.
Publicado: (2021)

Embryonic exposure to fentanyl induces behavioral changes and neurotoxicity in zebrafish larvae
por: Wang, Binjie, et al.
Publicado: (2022)

Identification and characterization of a novel zebrafish (Danio rerio) pentraxin–carbonic anhydrase
por: Patrikainen, Maarit S., et al.
Publicado: (2017)

Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR
por: Musada, Ganeswara Rao, et al.
Publicado: (2016)

Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR
por: Trang, Duong Thu, et al.
Publicado: (2022)

Long-term clinical prognosis of 335 infant single-gene positive FEVR cases
por: Chen, Chunli, et al.
Publicado: (2022)

A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR
por: Peng, Li, et al.
Publicado: (2022)

At R407/R408
Publicado: (1974)

Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases"
por: Collin, Rob W.J., et al.
Publicado: (2020)

Diagnosis of complicated FEVR preoperatively and intra−/post-operatively: characteristics and risk factors for diagnostic timing
por: Xia, Fengjie, et al.
Publicado: (2019)

Development and origins of Zebrafish ocular vasculature
por: Kaufman, Rivka, et al.
Publicado: (2015)

Do N-arachidonyl-glycine (NA-glycine) and 2-arachidonoyl glycerol (2-AG) share mode of action and the binding site on the β(2) subunit of GABA(A) receptors?
por: Baur, Roland, et al.
Publicado: (2013)

Data on association of the variation (rs1344706) in the ZNF804A gene with schizophrenia and its symptoms in the Russian population
por: Lezheiko, T.V., et al.
Publicado: (2019)

Genetic determinants of hyaloid and retinal vasculature in zebrafish
por: Alvarez, Yolanda, et al.
Publicado: (2007)

Enhancement and Segmentation Workflow for the Developing Zebrafish Vasculature †
por: Kugler, Elisabeth, et al.
Publicado: (2019)

Species-Dependent Splice Recognition of a Cryptic Exon Resulting from a Recurrent Intronic CEP290 Mutation that Causes Congenital Blindness
por: Garanto, Alejandro, et al.
Publicado: (2015)

ScanFold 2.0: a rapid approach for identifying potential structured RNA targets in genomes and transcriptomes
por: Andrews, Ryan J., et al.
Publicado: (2022)

Partners in crime: MicroRNA408 and peptide miPEP408 negatively regulate arsenic and low sulfur tolerance
por: Ku, Yee-Shan
Publicado: (2023)

Unexpected CEP290 mRNA Splicing in a Humanized Knock-In Mouse Model for Leber Congenital Amaurosis
por: Garanto, Alejandro, et al.
Publicado: (2013)

Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology
por: Stemerdink, Merel, et al.
Publicado: (2023)

Single-Cell Characterization of the Frizzled 5 (Fz5) Mutant Mouse and Human Persistent Fetal Vasculature (PFV)
por: Chen, Yuanyuan, et al.
Publicado: (2023)

Le Fevre’s Diagnosis: A Manual on Physical Diagnosis, Including Diseases of the Thoracic and Abdominal Organs. For Students and Physicians
Publicado: (1906)

Memorandum: plans of experiment R 407-408
por: CERN. Geneva. Intersecting Storage-Rings Committee
Publicado: (1974)

Memorandum: Collaboration between Experiments 407 and 408
por: CERN. Geneva. Intersecting Storage-Rings Committee
Publicado: (1973)

The transcriptional activator ZNF143 is essential for normal development in zebrafish
por: Halbig, Kari M, et al.
Publicado: (2012)

Calcitriol and non-calcemic vitamin D analogue, 22-oxacalcitriol, attenuate developmental and pathological choroidal vasculature angiogenesis ex vivo and in vivo
por: Merrigan, Stephanie L., et al.
Publicado: (2020)

Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges
por: Vázquez-Domínguez, Irene, et al.
Publicado: (2019)

Expression and function of ATP-dependent potassium channels in zebrafish islet β-cells
por: Emfinger, Christopher H., et al.
Publicado: (2017)

Measurements of the spin and nuclear magnetic moment of the 408 msec 20Na
por: Bonn, J, et al.
Publicado: (1970)

ABC transporter functions as a pacemaker for sequestration of plant glucosides in leaf beetles
por: Strauss, Anja S, et al.
Publicado: (2013)

The role of vasculature and blood circulation in zebrafish swimbladder development
por: Winata, Cecilia Lanny, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_pjmsaou7idmpkahsa0medee4sd