Complement factor H-related hybrid protein deregulates complement in dense deposit disease.
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Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GNComplement System Part II: Role in ImmunityFactor H Family Proteins in Complement Evasion of Microorganisms.New insights into disease-specific absence of complement factor H related protein C in mouse models of spontaneous autoimmune diseasesDefining the complement biomarker profile of C3 glomerulopathyAnnexin A2 Enhances Complement Activation by Inhibiting Factor HDistinct roles for the complement regulators factor H and Crry in protection of the kidney from injury.The Genetics of Ultra-Rare Renal Disease.Kidney Disease Caused by Dysregulation of the Complement Alternative Pathway: An Etiologic Approach.Rituximab for Treatment of Membranoproliferative Glomerulonephritis and C3 Glomerulopathies.Retinal disease in the C3 glomerulopathies and the risk of impaired vision.From orphan drugs to adopted therapies: Advancing C3-targeted intervention to the clinical stage.The complement factor H-related proteins.C3 glomerulopathy.Complement C3-Targeted Therapy: Replacing Long-Held Assertions with Evidence-Based Discovery.Circulating complement factor H-related proteins 1 and 5 correlate with disease activity in IgA nephropathy.Factor H-related protein 5 interacts with pentraxin 3 and the extracellular matrix and modulates complement activation.Update on C3 glomerulopathy.Complement Factor H-Related 5-Hybrid Proteins Anchor Properdin and Activate Complement at Self-Surfaces.Rare Variants in the Complement Factor H-Related Protein 5 Gene Contribute to Genetic Susceptibility to IgA Nephropathy.The Murine Factor H-Related Protein FHR-B Promotes Complement ActivationKidney transplant outcomes in familial C3 glomerulopathy.Factor H-Related (FHR)-1 and FHR-2 Form Homo- and Heterodimers, while FHR-5 Circulates Only As Homodimer in Human Plasma.C4 Nephritic Factors in C3 Glomerulopathy: A Case Series.The MFHR1 Fusion Protein Is a Novel Synthetic Multitarget Complement Inhibitor with Therapeutic Potential.Diseases of complement dysregulation-an overview.Functional Characterization of the Disease-Associated N-Terminal Complement Factor H Mutation W198R.An Engineered Complement Factor H Construct for Treatment of C3 Glomerulopathy.C3 Glomerulopathy.Management of hemolytic uremic syndromeThrombotic microangiopathy after renal transplantation: Current insights in and recurrent diseaseReference Intervals of Factor H and Factor H-Related Proteins in Healthy Children
P2860
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P2860
Complement factor H-related hybrid protein deregulates complement in dense deposit disease.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Complement factor H-related hy ...... ment in dense deposit disease.
@en
type
label
Complement factor H-related hy ...... ment in dense deposit disease.
@en
prefLabel
Complement factor H-related hy ...... ment in dense deposit disease.
@en
P2093
P2860
P356
P1476
Complement factor H-related hy ...... ment in dense deposit disease.
@en
P2093
Andrea Hartmann
Barbara Uzonyi
Christian Hugo
Christine Skerka
Hannes U Eberhardt
Kerstin Amann
Michael Kirschfink
Michael Wiesener
Tim Goodship
P2860
P304
P356
10.1172/JCI71866
P407
P577
2013-12-16T00:00:00Z