19741247

Source:http://linkedlifedata.com/resource/pubmed/id/19741247

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0035304, umls-concept:C0035499, umls-concept:C0205082, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1314792
pubmed:issue	2
pubmed:dateCreated	2010-1-19
pubmed:abstractText	To identify a new mouse mutation developing early-onset dominant retinal degeneration, to determine the causative gene mutation, and to investigate the underlying mechanism.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/EY013849, http://linkedlifedata.com/resource/pubmed/grant/EY016493
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7703701
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ethylnitrosourea, http://linkedlifedata.com/resource/pubmed/chemical/Rhodopsin
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1552-5783
pubmed:author	pubmed-author:BeutlerBruceB, pubmed-author:FlanneryJohn GJG, pubmed-author:GongXiaohuaX, pubmed-author:LüZ BZB, pubmed-author:LiuHaiquanH, pubmed-author:RidgeKevin DKD, pubmed-author:WangMengM, pubmed-author:XiaChun-HongCH
pubmed:issnType	Electronic
pubmed:volume	51
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1059-65
pubmed:dateRevised	2010-9-27
pubmed:meshHeading	pubmed-meshheading:19741247-Animals, pubmed-meshheading:19741247-Base Sequence, pubmed-meshheading:19741247-Blotting, Western, pubmed-meshheading:19741247-DNA Mutational Analysis, pubmed-meshheading:19741247-Electroretinography, pubmed-meshheading:19741247-Ethylnitrosourea, pubmed-meshheading:19741247-Genes, Dominant, pubmed-meshheading:19741247-Genome-Wide Association Study, pubmed-meshheading:19741247-Immunohistochemistry, pubmed-meshheading:19741247-Mice, pubmed-meshheading:19741247-Mice, Inbred C57BL, pubmed-meshheading:19741247-Mice, Knockout, pubmed-meshheading:19741247-Mice, Mutant Strains, pubmed-meshheading:19741247-Molecular Sequence Data, pubmed-meshheading:19741247-Mutagenesis, pubmed-meshheading:19741247-Ophthalmoscopy, pubmed-meshheading:19741247-Phenotype, pubmed-meshheading:19741247-Photoreceptor Cells, Vertebrate, pubmed-meshheading:19741247-Point Mutation, pubmed-meshheading:19741247-Protein Structure, Secondary, pubmed-meshheading:19741247-Retinal Degeneration, pubmed-meshheading:19741247-Rhodopsin
pubmed:year	2010
pubmed:articleTitle	Severe retinal degeneration caused by a novel rhodopsin mutation.
pubmed:affiliation	Vision Science Program and School of Optometry, University of California, Berkeley, Berkeley, California 94720-2020, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural