Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2011-5-4
pubmed:abstractText
High myopia is a severe hereditary ocular disease leading to blindness. LAMA1 (alpha subunit of laminin) is a promising candidate gene for high myopia present in the MYP2 (myopia 2) region. The purpose of this study was to determine if high myopia is associated with single nucleotide polymorphism (SNP) variants in LAMA1 in Chinese subjects.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-10845580, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-10937558, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-11133850, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-11713414, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-11734523, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-12183620, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-12592049, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-12601022, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1424721, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-14556208, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1496333, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1521568, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-15723005, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-15905314, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-17048038, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1714537, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-17532759, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1937488, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-19668483, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-19744728, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-1985485, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-2049067, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-2265680, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-2562517, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-2591971, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-3848400, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-5087475, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-6358100, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-6667766, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-6678372, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-7533533, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-7610587, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-7781741, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-8801636, http://linkedlifedata.com/resource/pubmed/commentcorrection/21541277-9634508
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1003-10
pubmed:meshHeading
pubmed-meshheading:21541277-Adult, pubmed-meshheading:21541277-Asian Continental Ancestry Group, pubmed-meshheading:21541277-Case-Control Studies, pubmed-meshheading:21541277-Cornea, pubmed-meshheading:21541277-DNA, pubmed-meshheading:21541277-DNA Primers, pubmed-meshheading:21541277-Female, pubmed-meshheading:21541277-Gene Expression, pubmed-meshheading:21541277-Gene Frequency, pubmed-meshheading:21541277-Genetic Diseases, Inborn, pubmed-meshheading:21541277-Genetic Predisposition to Disease, pubmed-meshheading:21541277-Genotype, pubmed-meshheading:21541277-Humans, pubmed-meshheading:21541277-Laminin, pubmed-meshheading:21541277-Linkage Disequilibrium, pubmed-meshheading:21541277-Male, pubmed-meshheading:21541277-Middle Aged, pubmed-meshheading:21541277-Myopia, pubmed-meshheading:21541277-Polymerase Chain Reaction, pubmed-meshheading:21541277-Polymorphism, Single Nucleotide, pubmed-meshheading:21541277-Promoter Regions, Genetic
pubmed:year
2011
pubmed:articleTitle
The association of a single nucleotide polymorphism in the promoter region of the LAMA1 gene with susceptibility to Chinese high myopia.
pubmed:affiliation
Eye Center of Beijing Tongren Hospital of Capital Medical University, Beijing Ophthalmology & Visual Sciences Key Lab, Beijing, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't