Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-2-3
pubmed:abstractText
It is now generally admitted that penetrance of the common HFE p.C282Y/p.C282Y genotype is incomplete, and identification of modifier genes is the concern of a growing number of research projects. We recently identified a significant association between pretherapeutic serum ferritin level and the common rs235756 single nucleotide polymorphism (SNP) of the BMP2 gene region. Our results further suggested an interactive effect between the BMP2 rs235756 SNP and the rs16827043 SNP in HJV, with a small additive effect of the rs4901474 SNP in BMP4.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1096-0961
pubmed:author
pubmed:copyrightInfo
Copyright 2009 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
34-7
pubmed:meshHeading
pubmed-meshheading:19879168-Adult, pubmed-meshheading:19879168-Alcohol Drinking, pubmed-meshheading:19879168-Amino Acid Substitution, pubmed-meshheading:19879168-Biological Markers, pubmed-meshheading:19879168-Bone Morphogenetic Protein 2, pubmed-meshheading:19879168-Cohort Studies, pubmed-meshheading:19879168-Female, pubmed-meshheading:19879168-Ferritins, pubmed-meshheading:19879168-Follow-Up Studies, pubmed-meshheading:19879168-France, pubmed-meshheading:19879168-Gene Frequency, pubmed-meshheading:19879168-Genetic Association Studies, pubmed-meshheading:19879168-Hemochromatosis, pubmed-meshheading:19879168-Histocompatibility Antigens Class I, pubmed-meshheading:19879168-Homozygote, pubmed-meshheading:19879168-Humans, pubmed-meshheading:19879168-Iron, pubmed-meshheading:19879168-Male, pubmed-meshheading:19879168-Membrane Proteins, pubmed-meshheading:19879168-Middle Aged, pubmed-meshheading:19879168-Penetrance, pubmed-meshheading:19879168-Phlebotomy, pubmed-meshheading:19879168-Polymorphism, Single Nucleotide, pubmed-meshheading:19879168-Severity of Illness Index
pubmed:year
2010
pubmed:articleTitle
A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up study.
pubmed:affiliation
IRD - UR010, Paris, France.
pubmed:publicationType
Journal Article