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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2003-5-1
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pubmed:abstractText |
To determine the full-length sequence of a gene with similarity to RP1 and to screen for mutations in this newly characterized gene, named retinitis pigmentosa 1-like 1(RP1L1). Since mutations in the RP1 gene cause autosomal dominant retinitis pigmentosa, it is possible that mutations in RP1's most sequence similar relative, RP1L1, may also be a cause of inherited retinal degeneration.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10391211,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10391212,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10401003,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10484783,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10770842,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-10946000,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-11139241,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-11545739,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-11756666,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-8682515,
http://linkedlifedata.com/resource/pubmed/commentcorrection/12724644-9475085
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1090-0535
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pubmed:author |
pubmed-author:BirchDavid GDG,
pubmed-author:BowneSara JSJ,
pubmed-author:DaigerStephen PSP,
pubmed-author:DonovanDanyel DDD,
pubmed-author:HeckenlivelyJohn RJR,
pubmed-author:HuangQianQ,
pubmed-author:Hughbanks-WheatonDiannaD,
pubmed-author:HumphriesPeterP,
pubmed-author:KennanAvrilA,
pubmed-author:KuzT JTJ,
pubmed-author:MaloneKimberly AKA,
pubmed-author:PierceEric AEA,
pubmed-author:SullivanLori SLS,
pubmed-author:ZuoJianJ
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pubmed:issnType |
Electronic
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pubmed:day |
24
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
129-37
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:12724644-Amino Acid Sequence,
pubmed-meshheading:12724644-Animals,
pubmed-meshheading:12724644-Base Sequence,
pubmed-meshheading:12724644-Chromosomes, Human, Pair 8,
pubmed-meshheading:12724644-DNA Mutational Analysis,
pubmed-meshheading:12724644-Electrophoresis, Agar Gel,
pubmed-meshheading:12724644-Eye Proteins,
pubmed-meshheading:12724644-Genes, Dominant,
pubmed-meshheading:12724644-Humans,
pubmed-meshheading:12724644-In Situ Hybridization,
pubmed-meshheading:12724644-Mice,
pubmed-meshheading:12724644-Molecular Sequence Data,
pubmed-meshheading:12724644-Mutation,
pubmed-meshheading:12724644-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:12724644-RNA, Messenger,
pubmed-meshheading:12724644-Retinitis Pigmentosa,
pubmed-meshheading:12724644-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:12724644-Sequence Homology, Amino Acid
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pubmed:year |
2003
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pubmed:articleTitle |
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.
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pubmed:affiliation |
Human Genetics Center, University of Texas Health Science Center at Houston, TX 77225, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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