|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
9743
|
|
pubmed:dateCreated |
2010-9-6
|
|
pubmed:abstractText |
Complement is a key component of the innate immune system, and variation in genes that regulate its activation is associated with renal and other disease. We aimed to establish the genetic basis for a familial disorder of complement regulation associated with persistent microscopic haematuria, recurrent macroscopic haematuria, glomerulonephritis, and progressive renal failure.
|
|
pubmed:grant |
|
|
pubmed:commentsCorrections |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Sep
|
|
pubmed:issn |
1474-547X
|
|
pubmed:author |
pubmed-author:AthanasiouYiannisY,
pubmed-author:CookH TerenceHT,
pubmed-author:DBB,
pubmed-author:DeltasConstantinosC,
pubmed-author:Frémeaux-BacchiVéroniqueV,
pubmed-author:GaleDaniel PDP,
pubmed-author:HadjisavvasAndreasA,
pubmed-author:Martinez-BarricarteRubénR,
pubmed-author:MaxwellPatrick HPH,
pubmed-author:McLeanAdam GAG,
pubmed-author:PalmerAndrewA,
pubmed-author:PickeringMatthew CMC,
pubmed-author:PieridesAlkisA,
pubmed-author:PuseyCharles DCD,
pubmed-author:VoskaridesKonstantinosK,
pubmed-author:de CordobaSantiago RodriguezSR,
pubmed-author:de JorgeElena GoicoecheaEG
|
|
pubmed:copyrightInfo |
Copyright 2010 Elsevier Ltd. All rights reserved.
|
|
pubmed:issnType |
Electronic
|
|
pubmed:day |
4
|
|
pubmed:volume |
376
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
794-801
|
|
pubmed:dateRevised |
2010-12-3
|
|
pubmed:meshHeading |
pubmed-meshheading:20800271-Adult,
pubmed-meshheading:20800271-Aged,
pubmed-meshheading:20800271-Blood Proteins,
pubmed-meshheading:20800271-Complement C5,
pubmed-meshheading:20800271-Complement Factor H,
pubmed-meshheading:20800271-Complement System Proteins,
pubmed-meshheading:20800271-Cyprus,
pubmed-meshheading:20800271-Endemic Diseases,
pubmed-meshheading:20800271-Female,
pubmed-meshheading:20800271-Genome-Wide Association Study,
pubmed-meshheading:20800271-Glomerulonephritis,
pubmed-meshheading:20800271-Humans,
pubmed-meshheading:20800271-Kidney Failure, Chronic,
pubmed-meshheading:20800271-Male,
pubmed-meshheading:20800271-Middle Aged,
pubmed-meshheading:20800271-Mutation,
pubmed-meshheading:20800271-Pedigree,
pubmed-meshheading:20800271-Polymorphism, Single Nucleotide
|
|
pubmed:year |
2010
|
|
pubmed:articleTitle |
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis.
|
|
pubmed:affiliation |
Division of Medicine, University College, London, UK.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
