Cargando…

REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival

In retinal photoreceptors, vectorial transport of cargo is critical for transduction of visual signals, and defects in intracellular trafficking can lead to photoreceptor degeneration and vision impairment. Molecular signatures associated with routing of transport vesicles in photoreceptors are poor...

Descripción completa

Detalles Bibliográficos
Autores principales:	Veleri, Shobi, Nellissery, Jacob, Mishra, Bibhudatta, Manjunath, Souparnika H., Brooks, Matthew J., Dong, Lijin, Nagashima, Kunio, Qian, Haohua, Gao, Chun, Sergeev, Yuri V., Huang, Xiu-Feng, Qu, Jia, Lu, Fan, Cideciyan, Artur V., Li, Tiansen, Jin, Zi-Bing, Fariss, Robert N., Ratnapriya, Rinki, Jacobson, Samuel G., Swaroop, Anand
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2017
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458339/ https://www.ncbi.nlm.nih.gov/pubmed/28369466 http://dx.doi.org/10.1093/hmg/ddx111

Ejemplares similares

Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis
por: Veleri, Shobi, et al.
Publicado: (2014)

Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration
por: Hargrove-Grimes, Passley, et al.
Publicado: (2020)

Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing
por: Ratnapriya, Rinki, et al.
Publicado: (2013)

Neurotropism of SARS-CoV-2 and neurological diseases of the central nervous system in COVID-19 patients
por: Veleri, Shobi
Publicado: (2021)

A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration
por: Ratnapriya, Rinki, et al.
Publicado: (2021)

Accelerated Development of Rod Photoreceptors in Retinal Organoids Derived from Human Pluripotent Stem Cells by Supplementation with 9-cis Retinal
por: Kelley, Ryan A., et al.
Publicado: (2020)

Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins
por: Rachel, Rivka A, et al.
Publicado: (2012)

REEP3 and REEP4 determine the tubular morphology of the endoplasmic reticulum during mitosis
por: Kumar, Darshan, et al.
Publicado: (2019)

Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiology
por: Garafalo, Alexandra V., et al.
Publicado: (2021)

Biology and therapy of inherited retinal degenerative disease: insights from mouse models
por: Veleri, Shobi, et al.
Publicado: (2015)

Three-dimensional retinal organoids from mouse pluripotent stem cells mimic in vivo development with enhanced stratification and rod photoreceptor differentiation
por: Chen, Holly Yu, et al.
Publicado: (2016)

Frmpd1 Facilitates Trafficking of G-Protein Transducin and Modulates Synaptic Function in Rod Photoreceptors of Mammalian Retina
por: Campla, Christie K., et al.
Publicado: (2022)

The accessory proteins REEP5 and REEP6 refine CXCR1-mediated cellular responses and lung cancer progression
por: Park, Cho Rong, et al.
Publicado: (2016)

Light-Induced Thickening of Photoreceptor Outer Segment Layer Detected by Ultra-High Resolution OCT Imaging
por: Li, Yichao, et al.
Publicado: (2016)

Pias3 is necessary for dorso-ventral patterning and visual response of retinal cones but is not required for rod photoreceptor differentiation
por: Campla, Christie K., et al.
Publicado: (2017)

Molecular Chaperone Dysfunction in Neurodegenerative Diseases and Effects of Curcumin
por: Maiti, Panchanan, et al.
Publicado: (2014)

Divergent Effects of HSP70 Overexpression in Photoreceptors During Inherited Retinal Degeneration
por: Jiang, Ke, et al.
Publicado: (2020)

EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression
por: McGuigan, David B., et al.
Publicado: (2017)

Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations
por: Cideciyan, Artur V., et al.
Publicado: (2020)

Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration
por: Zhao, Lian, et al.
Publicado: (2015)

Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing
por: Roberts, Lisa, et al.
Publicado: (2016)

Mucociliary Respiratory Epithelium Integrity in Molecular Defense and Susceptibility to Pulmonary Viral Infections
por: Adivitiya,, et al.
Publicado: (2021)

Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal
por: Kaya, Koray D., et al.
Publicado: (2019)

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
por: Arno, Gavin, et al.
Publicado: (2016)

Further supporting evidence for REEP1 phenotypic and allelic heterogeneity
por: Maroofian, Reza, et al.
Publicado: (2019)

Converging Role for REEP1/SPG31 in Oxidative Stress
por: Naef, Valentina, et al.
Publicado: (2023)

Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects
por: Veleri, Shobi, et al.
Publicado: (2012)

Mitochondrial Respiration in Outer Retina Contributes to Light-Evoked Increase in Hydration In Vivo
por: Berkowitz, Bruce A., et al.
Publicado: (2018)

Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defects
por: Chen, Holly Y, et al.
Publicado: (2023)

Regulation of Noncoding Transcriptome in Developing Photoreceptors by Rod Differentiation Factor NRL
por: Zelinger, Lina, et al.
Publicado: (2017)

Targeted Expression of Retinoschisin by Retinal Bipolar Cells in XLRS Promotes Resolution of Retinoschisis Cysts Sans RS1 From Photoreceptors
por: Vijayasarathy, Camasamudram, et al.
Publicado: (2022)

Centrosomal protein CP110 controls maturation of the mother centriole during cilia biogenesis
por: Yadav, Sharda Prasad, et al.
Publicado: (2016)

Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy
por: Schottmann, Gudrun, et al.
Publicado: (2015)

De novo REEP2 missense mutation in pure hereditary spastic paraplegia
por: Roda, Ricardo H., et al.
Publicado: (2017)

Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
por: Ma, Xinran, et al.
Publicado: (2020)

Naringenin Ameliorates Drosophila ReepA Hereditary Spastic Paraplegia-Linked Phenotypes
por: Napoli, Barbara, et al.
Publicado: (2019)

Antiviral, immunomodulatory, and anticoagulant effects of quercetin and its derivatives: Potential role in prevention and management of COVID-19
por: Manjunath, Souparnika H., et al.
Publicado: (2022)

GATD3A, a mitochondrial deglycase with evolutionary origins from gammaproteobacteria, restricts the formation of advanced glycation end products
por: Smith, Andrew J., et al.
Publicado: (2022)

Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31
por: Fisher, K. M., et al.
Publicado: (2013)

REEP5 depletion causes sarco-endoplasmic reticulum vacuolization and cardiac functional defects
por: Lee, Shin-Haw, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_c6beb84es8dhrb9qkjhfge2i0a