Metabolic Studies of the Third Component of Complement and the Glycine-Rich Beta Glycoprotein in Patients with Hypocomplementemia

scientific article published on June 1, 1974

Metabolic Studies of the Third Component of Complement and the Glycine-Rich Beta Glycoprotein in Patients with Hypocomplementemia is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1172/JCI107708
P953full work available at URLhttps://europepmc.org/articles/PMC302653
https://europepmc.org/articles/PMC302653?pdf=render
P932PMC publication ID302653
P698PubMed publication ID4830223
P5875ResearchGate publication ID18338877

P2093author name stringP. J. Lachmann
D. K. Peters
J. A. Charlesworth
D. G. Williams
E. Sherington
P2860cites workComplement studies in membrano-proliferative glomerulonephritisQ54310752
Metabolism of radio-labelled C3: effects of in vivo activation in rabbitsQ68918643
Metabolism of third complement component (C3) in nephritis. Involvement of the classic and alternate (properdin) pathways for complement activationQ69377011
The alternate pathway of complement activation. The role of C3 and its inactivator (KAF)Q69382920
Mesangiocapillary nephritis, partial lipodystrophy, and hypocomplementaemiaQ70000316
A method of trace iodination of proteins for immunologic studiesQ70063670
Decreased synthesis of the third component of complement (C3) in hypocomplementemic systemic lupus erythematosusQ70405893
Distribution and metabolism of I131 labeled proteins in manQ74607843
The theory of tracer experiments with 131I-labelled plasma proteinsQ74703080
ANTIGEN-ANTIBODY CROSSED ELECTROPHORESISQ78397474
Studies in vivo and in vitro on an abnormality in the metabolism of C3 in a patient with increased susceptibility to infectionQ24300424
Glomerular deposition of properdin in acute and chronic glomerulonephritis with hypocomplementemiaQ34058375
Alper CA, Rosen FS: Studies of the in vivo behavior of human C'3 in normal subjects and patientsQ34089408
Properdin and C3 Proactivator: Alternate Pathway Components in Human GlomerulonephritisQ34500930
The relationship of glycine-rich -glycoprotein to factor B in the properdin system and to the cobra factor-binding protein of huan serumQ36272793
Inactivator of the Third Component of Complement as an Inhibitor in the Properdin PathwayQ37496999
Analysis of Disappearance Time-Curves After Single Injection of Labelled ProteinsQ39925681
C3 proactivator convertase and its mode of actionQ42836051
Isolation and properties of a glycine-rich β-glycoprotein of human serumQ44467148
Hypocomplementemia with cutaneous vasculitis and arthritis. Possible immune complex syndromeQ44492309
Role of C3b in the breakdown of C3 in hypocomplementaemic mesangiocapillary glomerulonephritisQ44511852
Serum C'3 lytic system in patients with glomerulonephritisQ44885697
Chronic glomerulonephritis associated with low serum complement activity (chronic hypocomplementemic glomerulonephritis)Q45031766
C3 inactivating factor in the serum of a patient with chronic hypocomplementaemic proliferative glomerulo-nephritisQ46300652
Metabolism of the Third Component of Complement (C3) in Normal Human SubjectsQ47884717
Increased Susceptibility to Infection in a Patient with Type II Essential Hypercatabolism of C3Q48014058
The purification of specific antibody as F(ab')2 by the pepsin digestion of antigen-antibody precipitates, and its application to immunoglobulin and complement antigens.Q54310041
P433issue6
P407language of work or nameEnglishQ1860
P304page(s)1578-1587
P577publication date1974-06-01
P1433published inJournal of Clinical InvestigationQ3186904
P1476titleMetabolic Studies of the Third Component of Complement and the Glycine-Rich Beta Glycoprotein in Patients with Hypocomplementemia
P478volume53

Reverse relations

cites work (P2860)
Q35498749A quantitative lateral flow assay to detect complement activation in blood
Q67529957Activation of the alternative complement pathway in systemic lupus erythematosus
Q67653052Acute hepatitis: significance of changes in complement components
Q37138770Alpha 1-antitrypsin deficiency, complement activation, and chronic liver disease
Q66884828C3 metabolism in a patient with deficiency of the second component of complement (C2) and discoid lupus erythematosus
Q72823186C3 metabolism in acute glomerulonephritis: implications for sites of complement activation
Q35201919C3b inactivator in the rheumatic diseases. Measurement by radial immunodiffusion and by inhibition of formation of properdin pathway C3 convertase
Q67277366Change in serum properdin factor B phenotype following human orthoptic liver transplantation
Q58808226Circulating C3, C4, and C3 Split Products (C3c and C3d) During Normal Pregnancy*
Q37044336Circulating complement breakdown products in patients with rheumatoid arthritis. Correlation between plasma C3d, circulating immune complexes, and clinical activity
Q41035669Circulating immune complexes and C3d in human parasitosis
Q36616293Clinical application of a new nephelometric technique to measure complement activation
Q35196683Clinical significance of serum properdin levels and properdin deposition in the dermal-epidermal junction in systemic lupus erythematosus
Q39809852Clinical utility of complement assessment
Q68811673Complement (C3) metabolism in systemic lupus erythematosus in relation to the disease course
Q71294704Complement activating cryoglobulins in the nephritis of systemic lupus erythematosus
Q37246497Complement activation by cellulosic dialysis membranes
Q33396528Complement activation during liver transplantation-special emphasis on patients with atypical hemolytic uremic syndrome
Q41731011Complement activation in asymptomatic patients with sickle cell anaemia
Q39429305Complement activation in migraine
Q67958586Complement activation in patients with renal failure as detected through the quantitation of fragments of the complement proteins C3, C5, and factor B
Q41188610Complement activation in pneumonia
Q34860585Complement activation profiles in disease
Q45162825Complement and the clinician
Q35194351Complement breakdown products in plasma from patients with systemic lupus erythematosus and patients with membranoproliferative or other glomerulonephritis
Q41365781Complement in cystic fibrosis
Q39487716Complement in the pathophysiology and diagnosis of human diseases
Q43724040Complement levels and C3 breakdown products in open-heart surgery: association of C3 conversion with the postpericardiotomy syndrome
Q70646458Complement split product C3d as an indicator of disease activity in systemic lupus erythematosus
Q72114120Correlation in rheumatoid arthritis of concentrations of plasma C3d, serum rheumatoid factor, immune complexes and C-reactive protein with each other and with clinical features of disease activity
Q43853170Correlations between serum factor B and C3b inactivator levels in normal subjects and in patients with infections, nephrosis and hypocomplementaemic glomerulonephritis.
Q41928296Cutaneous leishmaniasis: immune complex formation and necrosis in the acute phase
Q72122677Determination of the half-life of C3 in patients and its relation to the presence of C3-breakdown products and/or circulating immune complexes
Q70227589Development and clinical application of electroimmunoassays for the direct quantification of the complement C3 split products C3c and C3d
Q93523702Differences in the metabolism of C4 isotypes in patients with complement activation
Q72639251Double-decker rocket immunoelectrophoresis for direct quantitation of complement C3 split products with C3d specificities in plasma
Q36130596Effects on serum complement of normal and pre-eclamptic pregnancy and of oral contraceptives
Q72631340Evaluation of alternative pathway and factor B haemolytic activities in patients with systemic lupus erythematosus: correlations with the alternative pathway regulatory proteins
Q41117627Experimental immune glomerulonephritis induced in the rabbit with streptococcal vaccine
Q24651118Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice
Q33890087Generation of complement protein C3 deficient pigs by CRISPR/Cas9-mediated gene targeting
Q69867245Genetically determined low C4: a predisposing factor to autoimmune chronic active hepatitis
Q57747428Hereditary C3 hypocomplementemia in the rabbit
Q34541825Human fibronectin metabolism
Q70567912Hypocomplementaemia due to a genetic deficiency of beta 1H globulin
Q44481073Hypocomplementemia in a newborn infant caused by placental transfer of C3 nephritic factor
Q39644143Identification of nephritic factor as an immunoglobulin
Q35887592Idiopathic membranoproliferative glomerulonephritis in childhood
Q40932039Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (Type I MPGN)
Q74600355Infection in systemic lupus erythematosus
Q39714582Inherited deficiencies of complement in man
Q41878114Measles infection. Involvement of the complement system
Q67445830Membranoproliferative Nephritis and C3NeF
Q69633523Membranoproliferative glomerulonephritis, type II and partial lipodystrophy in an adult
Q71761794Meningococcal meningitis associated with persistent hypocomplementaemia due to circulating C3 nephritic factor
Q45246565Mesangiocapillary glomerulonephritis associated with meningococcal meningitis, C3 nephritic factor and persistently low complement C3 and C5.
Q52779350Metabolic studies of C3 in man
Q35817146Metabolic studies of radioiodinated serum amyloid P component in normal subjects and patients with systemic amyloidosis
Q66992247Metabolism of human beta 1H: studies in man and experimental animals
Q34482222Metabolism of properdin in normal subjects and patients with renal disease
Q37043934Metabolism of the fifth component of complement, and its relation to metabolism of the third component, in patients with complement activation
Q39537318Modulation of the properdin amplification loop in membranoproliferative and other forms of glomerulonephritis
Q70586995Molecular analysis of C3 allotypes in patients with nephritic factor
Q28317990Nephritic factor: Description of a new quantitative assay and findings in glomerulonephritis
Q67574406Normal complement in early poststreptococcal glomerulonephritis
Q69760964Opsonins and dysopsonins: an overview
Q39776393Pathogenesis and approaches to therapy of membranoproliferative glomerulonephritis
Q70228698Plasma C3d/C3 quotient as a parameter for in vivo complement activation
Q39688025Relative importance of C3b inactivator and beta 1H globulin in the modulation of the properdin amplification loop in systemic lupus erythematosus
Q68075258Relative value of serum C3 and C4 levels in predicting relapse in systemic lupus erythematosus
Q38724499Review: assessment of complement activation in clinical immunology laboratories: time for reappraisal?
Q33433754Self-nonself discrimination by the complement system
Q44817225Serum immune complexes in membranoproliferative and other glomerulonephritides
Q44396159Significance of complement-positive Coombs test in patients with glomerular disease
Q70033141Skin lesions, angio-oedema, and hypocomplementaemia
Q67507672Studies in vivo of cobra factor and murine C3
Q68370350Studies of serum complement in the hypocomplementaemic nephritides
Q67433383The Complement Abnormalities of Lipodystrophy
Q40487571The Complement System in Infectious Mononucleosis
Q40487563The Nail Patella Syndrome-A Report of a Family
Q67755681The cofactors required by C3 nephritic factor to generate a C3 convertase in vitro
Q69445277The complement system in type 1 (insulin-dependent) diabetes
Q40659228The in Vivo Metabolism of the Third Component of Complement in Systemic Lupus Erythematosus
Q33553504The in-vivo metabolism of C3 in ankylosing spondylitis
Q52767987The metabolism of C3 in adult coeliac disease.
Q70311157Thein vivometabolism of C3 in human glomerulonephritis and after renal transplantation

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