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Academic Journal

WITHDRAWN: Investigating the ERG a-wave and Retinal Diseases with Rod Equivalent Circuit Model Based on the APD.

Subjects: Retinal Diseases* ; Electroretinography*; Humans

  • Source: Biophysical journal [Biophys J] 2024 Aug 20; Vol. 123 (16), pp. 2644. Date of Electronic Publication: 2024 Aug 02.Publisher: Cell Press Country of Publication: United States NLM ID: 0370626 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Deep learning for precision medicine: Guiding laser therapy in ischemic retinal diseases.

  • Authors : Tan TF; Singapore National Eye Center, Singapore Eye Research Institute, Singapore, Singapore.; Chang SY

Subjects: Deep Learning* ; Retinal Diseases*/Retinal Diseases*/Retinal Diseases*/diagnostic imaging ; Retinal Diseases*/Retinal Diseases*/Retinal Diseases*/therapy

  • Source: Cell reports. Medicine [Cell Rep Med] 2023 Oct 17; Vol. 4 (10), pp. 101239.Publisher: Cell Press Country of Publication: United States NLM ID: 101766894 Publication Model: Print Cited Medium:

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Academic Journal

In vivo genome editing for inherited retinal disease: Opportunities and challenges.

  • Authors : Collin RWJ; Department of Human Genetics, Radboud Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: .; Leroy BP

Subjects: Gene Editing*/Gene Editing*/Gene Editing*/methods ; Retinal Diseases*/Retinal Diseases*/Retinal Diseases*/therapy ; Retinal Diseases*/Retinal Diseases*/Retinal Diseases*/genetics

  • Source: Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2024 Aug 07; Vol. 32 (8), pp. 2433-2434. Date of Electronic Publication: 2024 Jul 30.Publisher: Cell Press Country of Publication: United States NLM ID: 100890581 Publication Model: Print-Electronic Cited

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Academic Journal

Learning from Everyday Images Enables Expert-like Diagnosis of Retinal Diseases.

  • Authors : Rampasek L; University of Toronto, Department of Computer Science, Toronto, ON, Canada; The Hospital for Sick Children, Toronto, ON, Canada

Subjects: Deep Learning* ; Retinal Diseases*; Humans

  • Source: Cell [Cell] 2018 Feb 22; Vol. 172 (5), pp. 893-895.Publisher: Cell Press Country of Publication: United States NLM ID: 0413066 Publication Model: Print Cited Medium:

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Academic Journal

Pathological angiogenesis in retinopathy engages cellular senescence and is amenable to therapeutic elimination via BCL-xL inhibition.

  • Authors : Crespo-Garcia S; Department of Biochemistry, Maisonneuve-Rosemont Hospital Research Centre, University of Montreal, Montreal QC H1T 2M4, Canada.; Tsuruda PR

Subjects: Cellular Senescence*/Cellular Senescence*/Cellular Senescence*/drug effects; Retinal Diseases/Retinal Diseases/Retinal Diseases/*pathology ; bcl-X Protein/bcl-X Protein/bcl-X Protein/*metabolism

  • Source: Cell metabolism [Cell Metab] 2021 Apr 06; Vol. 33 (4), pp. 818-832.e7. Date of Electronic Publication: 2021 Feb 05.Publisher: Cell Press Country of Publication: United States NLM ID: 101233170 Publication Model: Print-Electronic Cited

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Academic Journal

PSCs Reveal PUFA-Provoked Mitochondrial Stress as a Central Node Potentiating RPE Degeneration in Bietti's Crystalline Dystrophy.

  • Authors : Zhang Z; Department of Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China; Prenatal Diagnostic Centre and Cord Blood Bank, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou 510623, China.

Subjects: Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/Corneal Dystrophies, Hereditary/*metabolism ; Epithelial Cells/Epithelial Cells/Epithelial Cells/*metabolism ; Fatty Acids, Unsaturated/Fatty Acids, Unsaturated/Fatty Acids, Unsaturated/*pharmacology Bietti Crystalline Dystrophy

  • Source: Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2020 Dec 02; Vol. 28 (12), pp. 2642-2661. Date of Electronic Publication: 2020 Jul 25.Publisher: Cell Press Country of Publication: United States NLM ID: 100890581 Publication Model: Print-Electronic Cited

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Academic Journal

Developmental Apoptosis Promotes a Disease-Related Gene Signature and Independence from CSF1R Signaling in Retinal Microglia.

  • Authors : Anderson SR; Department of Neurobiology and Anatomy, University of Utah, Salt Lake City, UT 84112, USA.; Roberts JM

Subjects: Apoptosis* ; Cell Differentiation* ; Signal Transduction*

  • Source: Cell reports [Cell Rep] 2019 May 14; Vol. 27 (7), pp. 2002-2013.e5.Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print Cited Medium:

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Academic Journal

Taking Stock of Retinal Gene Therapy: Looking Back and Moving Forward.

  • Authors : Bennett J; Center for Advanced Retinal and Ocular Therapeutics (CAROT) and F.M. Kirby Center for Molecular Ophthalmology, Scheie Eye Institute, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA. Electronic address: .

Subjects: Adenoviruses, Human/Adenoviruses, Human/Adenoviruses, Human/*genetics ; Eye Proteins/Eye Proteins/Eye Proteins/*genetics ; Genetic Therapy/Genetic Therapy/Genetic Therapy/*trends

  • Source: Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2017 May 03; Vol. 25 (5), pp. 1076-1094. Date of Electronic Publication: 2017 Apr 05.Publisher: Cell Press Country of Publication: United States NLM ID: 100890581 Publication Model: Print-Electronic Cited

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Academic Journal

BEST1: the Best Target for Gene and Cell Therapies.

  • Authors : Yang T; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, USA.; Justus S

Subjects: Cell- and Tissue-Based Therapy/Cell- and Tissue-Based Therapy/Cell- and Tissue-Based Therapy/*methods ; Chloride Channels/Chloride Channels/Chloride Channels/*genetics ; Eye Diseases, Hereditary/Eye Diseases, Hereditary/Eye Diseases, Hereditary/*genetics Bestrophinopathy

  • Source: Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2015 Dec; Vol. 23 (12), pp. 1805-9. Date of Electronic Publication: 2015 Sep 21.Publisher: Cell Press Country of Publication: United States NLM ID: 100890581 Publication Model: Print-Electronic Cited

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Academic Journal

Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.

Subjects: Abnormalities, Multiple/Abnormalities, Multiple/Abnormalities, Multiple/*genetics ; Arachnodactyly/Arachnodactyly/Arachnodactyly/*genetics ; Arthrogryposis/Arthrogryposis/Arthrogryposis/*genetics Gordon syndrome; Marden-Walker syndrome; Oculomelic amyoplasia

  • Source: American journal of human genetics [Am J Hum Genet] 2014 May 01; Vol. 94 (5), pp. 734-44. Date of Electronic Publication: 2014 Apr 10.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium:

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  • 1-10 of  202 results for ""RETINAL diseases""