A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.
about
Thrombotic microangiopathy and associated renal disorders.Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.Complement therapy in atypical haemolytic uraemic syndrome (aHUS).Cardiovascular complications in atypical haemolytic uraemic syndrome.A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.Atypical hemolytic uremic syndrome post-kidney transplantation: two case reports and review of the literatureA De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathiesCharacterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.Human factor H-related protein 2 (CFHR2) regulates complement activation.A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.Association among Complement Factor H Autoantibodies, Deletions of CFHR, and the Risk of Atypical Hemolytic Uremic Syndrome.Factor h: a complement regulator in health and disease, and a mediator of cellular interactions.Kidney Disease Caused by Dysregulation of the Complement Alternative Pathway: An Etiologic Approach.Fusion genes in malignant neoplastic disorders of haematopoietic system.Complement factor H in host defense and immune evasion.Complement Factor H-Related 5-Hybrid Proteins Anchor Properdin and Activate Complement at Self-Surfaces.All Things Complement.An extended mini-complement factor H molecule ameliorates experimental C3 glomerulopathy.Factor H Competitor Generated by Gene Conversion Events Associates with Atypical Hemolytic Uremic Syndrome.Hemolytic Uremic Syndrome in Pregnancy and Postpartum.Diseases of complement dysregulation-an overview.Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family.High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B.Atypical hemolytic uremic syndromeHemolytic uremic syndrome
P2860
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P2860
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.
description
2011 nî lūn-bûn
@nan
2011 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@ast
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@en
type
label
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@ast
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@en
prefLabel
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@ast
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@en
P2093
P50
P1433
P1476
A novel hybrid CFH/CFHR3 gene ...... cal hemolytic uremic syndrome.
@en
P2093
Claire L Harris
Denise Sadlier
Donal Reddan
Lisa Strain
Mary Waldron
Nigel J Francis
Timothy H J Goodship
P304
P356
10.1182/BLOOD-2011-03-339903
P407
P577
2011-11-04T00:00:00Z