Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-1-13
pubmed:abstractText
a genetic association study was performed on 126 patients with adolescent idiopathic scoliosis and 197 healthy controls from independent Hungarian pedigrees.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1528-1159
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
36
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E123-30
pubmed:meshHeading
pubmed-meshheading:21228692-Adolescent, pubmed-meshheading:21228692-Bone Morphogenetic Protein 4, pubmed-meshheading:21228692-Female, pubmed-meshheading:21228692-Gene Frequency, pubmed-meshheading:21228692-Gene Regulatory Networks, pubmed-meshheading:21228692-Genetic Predisposition to Disease, pubmed-meshheading:21228692-Genotype, pubmed-meshheading:21228692-Humans, pubmed-meshheading:21228692-Interleukin-6, pubmed-meshheading:21228692-Leptin, pubmed-meshheading:21228692-Male, pubmed-meshheading:21228692-Matrix Metalloproteinase 3, pubmed-meshheading:21228692-Models, Genetic, pubmed-meshheading:21228692-Polymorphism, Single Nucleotide, pubmed-meshheading:21228692-Promoter Regions, Genetic, pubmed-meshheading:21228692-Receptor, Melatonin, MT2, pubmed-meshheading:21228692-Scoliosis, pubmed-meshheading:21228692-Young Adult
pubmed:year
2011
pubmed:articleTitle
Association study of BMP4, IL6, Leptin, MMP3, and MTNR1B gene promoter polymorphisms and adolescent idiopathic scoliosis.
pubmed:affiliation
Institute of Genetics, Biological Research Center, Hungarian Academy of Sciences, Temesvári Körút 62, H-6726, Szeged, Hungary. morocz@brc.hu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't