|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2008-9-15
|
|
pubmed:abstractText |
Limited access to large samples precludes genome-wide association studies of rare but complex traits. To localize candidate genes with family-based genome-wide association, a novel exploratory analysis was first tested on 1774 major histocompatibility complex single nucleotide polymorphisms (SNPs) in 240 DNA samples from 80 children with primary liver transplantation and their biologic parents.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
1528-0012
|
|
pubmed:author |
pubmed-author:AshokkumarChethanC,
pubmed-author:BarmadaM MichaelMM,
pubmed-author:ChienNydiaN,
pubmed-author:EckertAndrewA,
pubmed-author:FerrellRobertR,
pubmed-author:FrackletonEdwardE,
pubmed-author:GlessnerJosephJ,
pubmed-author:HakonarsonHakonH,
pubmed-author:HiggsBrandon WBW,
pubmed-author:JaffeRonaldR,
pubmed-author:KimCeciliaC,
pubmed-author:MazariegosGeorgeG,
pubmed-author:PetroNancyN,
pubmed-author:SindhiRakeshR,
pubmed-author:TalukdarAnjanA,
pubmed-author:WeeksDaniel EDE,
pubmed-author:WilsonPatrickP
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
135
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
830-9, 839.e1-10
|
|
pubmed:dateRevised |
2010-12-3
|
|
pubmed:meshHeading |
pubmed-meshheading:18639552-B-Lymphocytes,
pubmed-meshheading:18639552-Cell Count,
pubmed-meshheading:18639552-Child,
pubmed-meshheading:18639552-Child, Preschool,
pubmed-meshheading:18639552-Female,
pubmed-meshheading:18639552-Gene Frequency,
pubmed-meshheading:18639552-Genetic Variation,
pubmed-meshheading:18639552-Genotype,
pubmed-meshheading:18639552-Graft Rejection,
pubmed-meshheading:18639552-HLA-D Antigens,
pubmed-meshheading:18639552-Humans,
pubmed-meshheading:18639552-Liver Transplantation,
pubmed-meshheading:18639552-Male,
pubmed-meshheading:18639552-Parents,
pubmed-meshheading:18639552-Polymorphism, Single Nucleotide
|
|
pubmed:year |
2008
|
|
pubmed:articleTitle |
Genetic variants in major histocompatibility complex-linked genes associate with pediatric liver transplant rejection.
|
|
pubmed:affiliation |
Hillman Center for Pediatric Transplantation, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA. Rakesh.Sindhi@chp.edu
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|
