Abstract
Cyril Mousseaux, Sandra Romero Ramirez, Pascale Testevuide, Renato C. Monteiro, David Buob, Laurent Mesnard, Patrick James Gleeson, Khalil El Karoui
Abstract
Authors
Institutions
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Absence of glomerular IgA1 deposition despite overexpression of galactose-deficient IgA1 in the B cell c1galt1 knockout mouse
10.1016/j.kint.2026.02.034 · 2026
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome
10.1038/s41431-022-01278-5 · 2023
Germline C1GALT1C1 mutation causes a multisystem chaperonopathy
10.1073/pnas.2211087120 · 2023
Glycans as a key factor in self and nonself discrimination: impact on the breach of immune tolerance
10.1002/1873-3468.14347 · 2022
Glomerular immunodeposits of patients with IgA nephropathy are enriched for IgG autoantibodies specific for galactose-deficient IgA1
10.1681/asn.2018111156 · 2019
The gut microbiota posttranslationally modifies IgA1 in autoimmune glomerulonephritis
10.1126/scitranslmed.adl6149 · 2024
The gut microbiota posttranslationally modifies IgA1 in autoimmune glomerulonephritis
10.1126/scitranslmed.adl6149 · doi-reference
Glomerular immunodeposits of patients with IgA nephropathy are enriched for IgG autoantibodies specific for galactose-deficient IgA1
Provenance
crossref
Confidence 100%
ror
Confidence 99%
ror
Confidence 99%
ror
Confidence 99%
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
datacite
Confidence 0%
10.1681/asn.2018111156 · doi-reference
Glycans as a key factor in self and nonself discrimination: impact on the breach of immune tolerance
10.1002/1873-3468.14347 · doi-reference
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome
10.1038/s41431-022-01278-5 · doi-reference
Germline C1GALT1C1 mutation causes a multisystem chaperonopathy
10.1073/pnas.2211087120 · doi-reference
Absence of glomerular IgA1 deposition despite overexpression of galactose-deficient IgA1 in the B cell c1galt1 knockout mouse
10.1016/j.kint.2026.02.034 · doi-reference