Cargando…

Author Correction: Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder

Detalles Bibliográficos
Autores principales:	Bonelli, Roberto, Jackson, Victoria E., Prasad, Aravind, Munro, Jacob E., Farashi, Samaneh, Heeren, Tjebo F. C., Pontikos, Nikolas, Scheppke, Lea, Friedlander, Martin, Egan, Catherine A., Allikmets, Rando, Ansell, Brendan R. E., Bahlo, Melanie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2021
Materias:	Author Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8035146/ https://www.ncbi.nlm.nih.gov/pubmed/33837246 http://dx.doi.org/10.1038/s42003-021-01972-y

Ejemplares similares

Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder
por: Bonelli, Roberto, et al.
Publicado: (2021)

Macular Telangiectasia Type 2: A Classification System Using MultiModal Imaging MacTel Project Report Number 10
por: Chew, Emily Y., et al.
Publicado: (2022)

Spectral domain OCT features in type 2 macular telangiectasia (type 2 MacTel): its relevance with clinical staging and visual acuity
por: Venkatesh, Ramesh, et al.
Publicado: (2022)

Specific Deoxyceramide Species Correlate with Expression of Macular Telangiectasia Type 2 (MacTel2) in a SPTLC2 Carrier HSAN1 Family
por: Wilson, Lindsey M. Q., et al.
Publicado: (2023)

iPSC–derived retinal pigmented epithelial cells from patients with macular telangiectasia show decreased mitochondrial function
por: Eade, Kevin T., et al.
Publicado: (2023)

Systemic lipid dysregulation is a risk factor for macular neurodegenerative disease
por: Bonelli, Roberto, et al.
Publicado: (2020)

Shared Features in Retinal Disorders With Involvement of Retinal Pigment Epithelium
por: Sparrow, Janet R., et al.
Publicado: (2021)

Spatial distribution of metabolites in the retina and its relevance to studies of metabolic retinal disorders
por: Bonelli, Roberto, et al.
Publicado: (2023)

A case of Mac Tel 2 with an unusual sub macular vitelliform lesion
por: Lekha, T., et al.
Publicado: (2015)

A survey of RNA editing at single-cell resolution links interneurons to schizophrenia and autism
por: Ansell, Brendan Robert E., et al.
Publicado: (2021)

Quantifying Fundus Autofluorescence in Patients With Retinitis Pigmentosa
por: Schuerch, Kaspar, et al.
Publicado: (2017)

Estimating Retinal Sensitivity Using Optical Coherence Tomography With Deep-Learning Algorithms in Macular Telangiectasia Type 2
por: Kihara, Yuka, et al.
Publicado: (2019)

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations
por: Cremers, Frans P.M., et al.
Publicado: (2020)

Functional Analysis of Retinal Flecks in Stargardt Disease
por: Verdina, Tommaso, et al.
Publicado: (2012)

Progressive Choriocapillaris Impairment in ABCA4 Maculopathy Is Secondary to Retinal Pigment Epithelium Atrophy
por: Jauregui, Ruben, et al.
Publicado: (2020)

Hyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal Degeneration
por: Sengillo, Jesse D., et al.
Publicado: (2019)

Retinal Pigment Epithelium Atrophy in Recessive Stargardt Disease as Measured by Short-Wavelength and Near-Infrared Autofluorescence
por: Jauregui, Ruben, et al.
Publicado: (2021)

Tel quel
por: Valéry, Paul, 1871-1945
Publicado: (1941)

Artificial intelligence in retinal disease: clinical application, challenges, and future directions
por: Daich Varela, Malena, et al.
Publicado: (2023)

Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
por: Su, Pei-Yin, et al.
Publicado: (2022)

Un tel potentiel !
por: Jenni, Peter
Publicado: (2004)

Tel quel 1 /
por: Valéry, Paul, 1871-1945
Publicado: (1977)

Predicting sex from retinal fundus photographs using automated deep learning
por: Korot, Edward, et al.
Publicado: (2021)

Panel‐based genetic testing for inherited retinal disease screening 176 genes
por: Sheck, Leo H. N., et al.
Publicado: (2021)

Using the Tevatron Electron Lens (TEL) as a Wire and other TEL Studies at FNAL
por: Zimmermann, Frank, et al.
Publicado: (2004)

The Leukemia-Associated Fusion Protein MN1-TEL Blocks TEL-Specific Recognition Sequences
por: ter Haar, W. Martijn, et al.
Publicado: (2012)

Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophy
por: Georgiou, Michalis, et al.
Publicado: (2021)

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

Genome sequencing and annotation of Serratia sp. strain TEL
por: Lephoto, Tiisetso E., et al.
Publicado: (2015)

State of the art spatial visualization of the response of neovascularisation to anti-vascular endothelial growth factor therapy
por: Okada, Mali, et al.
Publicado: (2022)

Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
por: Fiorentino, Alessia, et al.
Publicado: (2018)

The microbial biodiversity at the archeological site of Tel Megiddo (Israel)
por: Zhang, Yali, et al.
Publicado: (2023)

ReLayer: a Free, Online Tool for Extracting Retinal Thickness From Cross-Platform OCT Images
por: Ometto, Giovanni, et al.
Publicado: (2019)

Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques
por: Fujinami-Yokokawa, Yu, et al.
Publicado: (2019)

Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques
por: Fujinami-Yokokawa, Yu, et al.
Publicado: (2021)

Draft Whole-Genome Sequence of Serratia sp. Strain TEL, Associated with Oscheius sp. TEL-2014 (Nematoda: Rhabditidae) Isolated from a Grassland in South Africa
por: Lephoto, Tiisetso E., et al.
Publicado: (2015)

Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa
por: de Bruijn, Suzanne E., et al.
Publicado: (2020)

Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
por: Ávila-Fernández, Almudena, et al.
Publicado: (2010)

Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series
por: Oh, Jin Kyun, et al.
Publicado: (2022)

Construcción de bodega tipo tel-mex
por: Rivera Aguilar, Hugo
Publicado: (1992)

Cannot write session to /tmp/vufind_sessions/sess_c6urk9810eplmrc8nocuur6v8i