Oligosaccharide composition is similar in drusen and dense deposits in membranoproliferative glomerulonephritis type II.

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Oligosaccharide composition is similar in drusen and dense deposits in membranoproliferative glomerulonephritis type II. is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1035245947
P356DOI10.1038/KI.2008.658
P698PubMed publication ID19177159
P5875ResearchGate publication ID23957344

P50authorCarolyn J JonesQ64358807
P2093author name stringRichard E Bonshek
Ian S D Roberts
Colin D Short
Yvonne B D'souza
P2860cites workA common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationQ24523983
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)Q24655016
An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degenerationQ28190470
Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formationQ30671842
Complement and diseases: defective alternative pathway control results in kidney and eye diseasesQ33367362
Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literatureQ34293159
Complement activation and inflammatory processes in Drusen formation and age related macular degenerationQ34521109
Membranoproliferative glomerulonephritis type II (dense deposit disease): an updateQ36084453
New approaches to the treatment of dense deposit diseaseQ36860946
Fundus changes in (type II) mesangiocapillary glomerulonephritis simulating drusen: a histopathological reportQ42618487
Retinal changes associated with type 2 glomerulonephritisQ45064349
Fundus changes in membranoproliferative glomerulonephritis type II. A fluorescein angiographic study of 23 patientsQ68038284
Glycoproteins of drusen and drusen-like lesionsQ81230321
P433issue8
P407language of work or nameEnglishQ1860
P921main subjectoligosaccharideQ320607
glomerulonephritisQ605006
drusenQ1140528
membranoproliferative glomerulonephritisQ2299379
P304page(s)824-827
P577publication date2009-01-28
P1433published inKidney InternationalQ6404823
P1476titleOligosaccharide composition is similar in drusen and dense deposits in membranoproliferative glomerulonephritis type II
P478volume75

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cites work (P2860)
Q35750545Age-Related Macular Degeneration: A Disease of Systemic or Local Complement Dysregulation?
Q35580577Clinical features and outcomes of 98 children and adults with dense deposit disease.
Q34130746Glycoprotein hyposialylation gives rise to a nephrotic-like syndrome that is prevented by sialic acid administration in GNE V572L point-mutant mice
Q35449598High-speed ultrahigh-resolution OCT of Bruch's membrane in membranoproliferative glomerulonephritis type 2.
Q37510769Multimodal imaging of membranoproliferative glomerulonephritis type II.
Q47103639Multimodal imaging of retinal pigment epithelial detachments in patients with C3 glomerulopathy: case report and review of the literature
Q53070119Primary Glomerulonephritis with Unique C4d Deposition and Concurrent Non-infectious Intermediate Uveitis: a Case Report and Literature Review.
Q55710477Retinal Basal Laminar Deposits in Complement fH/fP Mouse Model of Dense Deposit Disease.
Q38749961Retinal disease in the C3 glomerulopathies and the risk of impaired vision.
Q47142300Retinal findings in membranoproliferative glomerulonephritis.

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