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Human Gene Therapy, ISSN 1043-0342, 10/2008, Volume 19, Issue 10, pp. 979 - 990
Leber congenital amaurosis (LCA) is a group of autosomal recessive blinding retinal diseases that are incurable. One molecular form is caused by mutations in... 
MEDICINE, RESEARCH & EXPERIMENTAL | VISUAL-ACUITY | CANINE MODEL | OPTICAL COHERENCE TOMOGRAPHY | VIRAL VECTORS | RETINAL-DETACHMENT REPAIR | NONHUMAN PRIMATE MODEL | CHILDHOOD BLINDNESS | THERAPY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IMMUNE-RESPONSES | GENETICS & HEREDITY | RETINITIS-PIGMENTOSA | Animal models | Adeno-associated virus | Toxicity | Clinical trials | Retina | Genomes | Light effects | Acuity | Visual perception | Eye | Thinning | Vision | Blindness | Serotypes | Pigments | Tomography | Mutation | Gene therapy | Age | Genetic Therapy | Follow-Up Studies | Humans | Genetic Diseases, Inborn | Male | retinoid isomerohydrolase | Dependovirus | Index Medicus | Dark Adaptation | Animals | Vision, Ocular | Adolescent | Adult | Female | Genetic Vectors | Eye Proteins | cis-trans-Isomerases | Carrier Proteins | Retina - metabolism | Genetic Vectors - administration & dosage | Blindness - metabolism | Genetic Diseases, Inborn - genetics | Blindness - pathology | Genetic Diseases, Inborn - pathology | Genetic Diseases, Inborn - therapy | Blindness - congenital | Genetic Diseases, Inborn - metabolism | Blindness - therapy | Eye Proteins - genetics | Genetic Vectors - metabolism | Blindness - genetics | Genetic Vectors - genetics | Carrier Proteins - genetics | Carrier Proteins - metabolism | Eye Proteins - metabolism | Usage | Care and treatment | Genetic vectors | Causes of | Genetic aspects | Retinal diseases | Methods
Journal Article
by Carss, Keren J and Carss, Keren and Arno, Gavin and Erwood, Marie and Stephens, Jonathan and Sanchis-Juan, Alba and Hull, Sarah and Megy, Karyn and Grozeva, Detelina and Dewhurst, Eleanor and Malka, Samantha and Plagnol, Vincent and Penkett, Christopher J and Penkett, Christopher and Stirrups, Kathleen and Rizzo, Roberta and Wright, Genevieve and Josifova, Dragana and Bitner-Glindzicz, Maria and Scott, Richard H and Scott, Richard and Clement, Emma and Allen, Hana Lango and Allen, Louise and Armstrong, Ruth and Brady, Angela F and Brady, Angie and Carmichael, Jenny and Chitre, Manali and Henderson, Robert H.H and Henderson, Robert and Hurst, Jane and MacLaren, Robert E and MacLaren, Robert and Murphy, Elaine and Paterson, Joan and Rosser, Elisabeth and Thompson, Dorothy A and Thompson, Dorothy and Wakeling, Emma and Ouwehand, Willem H and Michaelides, Michel and Moore, Anthony and Moore, Anthony T and Aitman, Timothy and Alachkar, Hana and Ali, Sonia and Allsup, David and Ambegaonkar, Gautum and Anderson, Julie and Antrobus, Richard and Arumugakani, Gururaj and Ashford, Sofie and Astle, William and Attwood, Antony and Austin, Steve and Bacchelli, Chiara and Bakchoul, Tamam and Bariana, Tadbir K and Baxendale, Helen and Bennett, David and Bethune, Claire and Bibi, Shahnaz and Bleda, Marta and Boggard, Harm and Bolton-Maggs, Paula and Booth, Claire and Bradley, John R and Brown, Matthew and Browning, Michael and Bryson, Christine and Burns, Siobhan and Calleja, Paul and Canham, Natalie and Caulfield, Mark and Chalmers, Elizabeth and Chandra, Anita and Chinnery, Patrick and Church, Colin and Clements-Brod, Naomi and Clowes, Virginia and Coghlan, Gerry and Collins, Peter and Cooper, Nichola and Creaser-Myers, Amanda and DaCosta, Rosa and Daugherty, Louise and Davies, Sophie and Davis, John and De Vries, Minka and Deegan, Patrick and Deevi, Sri V.V and Deshpande, Charu and Devlin, Lisa and Doffinger, Rainer and Dormand, Natalie and Drewe, Elizabeth and Edgar, David and Egner, William and Erber, Wendy N and ... and NIHR-BioResource Rare Dis and NIHR-BioResource Rare Diseases Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 01/2017, Volume 100, Issue 1, pp. 75 - 90
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2014, Volume 94, Issue 5, pp. 734 - 744
Journal Article
Nature Genetics, ISSN 1061-4036, 2010, Volume 42, Issue 10, pp. 840 - 850
Journal Article
Nature Neuroscience, ISSN 1097-6256, 03/2012, Volume 15, Issue 3, pp. 487 - 495
Brain circuits are assembled from a large variety of morphologically and functionally diverse cell types. It is not known how the intermingled cell types of an... 
COMMON VARIANTS | AMACRINE CELLS | ALZHEIMERS-DISEASE | IN-VIVO | MOUSE | GENE-EXPRESSION | MACULAR DEGENERATION | HUMAN FIBROBLASTS | DOPAMINERGIC-NEURONS | NEUROSCIENCES | PHOTOTRANSDUCTION | Brain | Transcription factors | Neurons | Circuits | Somatic cells | Nervous system | Retina | Eye diseases | Genomes | Gene expression | Atlases | Retinal Diseases | Potassium Channels, Voltage-Gated | Visual Pathways | Gene Expression | Receptors, Kainic Acid | Gluk2 kainate receptor | Gene Library | Mice, Inbred C57BL | Gja10 protein, mouse | Mice, Transgenic | Nerve Tissue Proteins | Patch-Clamp Techniques | Animals | Flow Cytometry | Membrane Potentials | Microarray Analysis | Connexins | Mice | Transcription Factors | Mutation | Eye Proteins | Cluster Analysis | Retinal Diseases - genetics | Membrane Potentials - genetics | Gene Expression - genetics | Visual Pathways - metabolism | Receptors, Kainic Acid - genetics | Neurons - classification | Retina - cytology | Neurons - physiology | Eye Proteins - genetics | Potassium Channels, Voltage-Gated - genetics | Microarray Analysis - methods | Connexins - genetics | Transcription Factors - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Eye Proteins - metabolism | Genes | Physiological aspects | Genetic aspects | Genetic transcription | Research | Risk factors | Index Medicus
Journal Article
2006, Essentials in ophthalmology, ISBN 9783540225942, xvi, 240
This volume of the "Essential Ophthalmology" series covers topical issues in pediatric ophthalmology. The well-structured text provides an update on current... 
Eye | Eye Diseases, Hereditary | Neuroophthalmology | Genetic aspects | Eye Diseases | Pediatric ophthalmology | Child | Diseases | Clinical & internal medicine | Pediatrics | Neurology | Nursing | Ophthalmology | Medicine & Public Health | Science, general | Neuroopthalmology
Book
Cell, ISSN 0092-8674, 2011, Volume 145, Issue 4, pp. 513 - 528
Journal Article