The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism

Investigative Ophthalmology and Visual Science

Volumn 52, Issue 6, 2011, Pages 3119-3128

  Thomas, Jennifer L ^a   Vihtelic, Thomas S ^b   dendekker, Aaron D ^c   Willer, Gregory ^c   Luo, Xixia ^a   Murphy, Taylor R ^b   Gregg, Ronald G ^c   Hyde, David R ^b   Thummel, Ryan ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NOTRE DAME   (United States)

^c UNIVERSITY OF LOUISVILLE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EYE PROTEIN; UNCLASSIFIED DRUG; VACUOLAR PROTEIN SORTING 11;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHEDIAK HIGASHI SYNDROME; CONTROLLED STUDY; EMBRYO; GENE; GENE EXPRESSION; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GRISCELLI SYNDROME; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MUTANT; NONHUMAN; OCULAR ALBINISM; PATHOGENESIS; PIGMENT EPITHELIUM; PIGMENTATION; PRIORITY JOURNAL; PROTEIN DEPLETION; RETINA DEVELOPMENT; RETINA DISEASE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TRANSMISSION ELECTRON MICROSCOPY; VACUOLAR PROTEIN SORTING 11 GENE; ZEBRA FISH;

ALBINISM, OCULOCUTANEOUS; ANIMALS; CHEDIAK-HIGASHI SYNDROME; DISEASE MODELS, ANIMAL; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; HEARING LOSS, SENSORINEURAL; HEPATOMEGALY; HERMANSKI-PUDLAK SYNDROME; IN SITU HYBRIDIZATION; MELANINS; MELANOPHORES; MELANOSOMES; MICROSCOPY, ELECTRON, TRANSMISSION; MODELS, GENETIC; MUTATION; PERICARDIAL EFFUSION; PIEBALDISM; PIGMENTATION DISORDERS; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINAL DISEASES; RETINAL PIGMENT EPITHELIUM; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SYNDROME; VESICULAR TRANSPORT PROTEINS; ZEBRAFISH; ZEBRAFISH PROTEINS;

EID: 79955951380     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-5957     Document Type: Article

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