IgG4-related diseases of the digestive tract
JM Löhr, M Vujasinovic, J Rosendahl… - Nature Reviews …, 2022 - nature.com
IgG4-related conditions affecting the digestive tract are part of a multi-organ fibro-
inflammatory disorder termed IgG4-related disease (IgG4-RD), with autoimmune pancreatitis …
inflammatory disorder termed IgG4-related disease (IgG4-RD), with autoimmune pancreatitis …
High serum IgG4 concentrations in patients with sclerosing pancreatitis
H Hamano, S Kawa, A Horiuchi, H Unno… - … England Journal of …, 2001 - Mass Medical Soc
Background Sclerosing pancreatitis is a unique form of pancreatitis that is characterized by
irregular narrowing of the main pancreatic duct, lymphoplasmacytic inflammation of the …
irregular narrowing of the main pancreatic duct, lymphoplasmacytic inflammation of the …
HLA DRB1* 0405-DQB1* 0401 haplotype is associated with autoimmune pancreatitis in the Japanese population
S Kawa, M Ota, K Yoshizawa, A Horiuchi, H Hamano… - Gastroenterology, 2002 - Elsevier
BACKGROUND & AIMS: Autoimmune pancreatitis is a distinctive disease entity
characterized by high serum immunoglobulin G4 concentrations. Because of the close …
characterized by high serum immunoglobulin G4 concentrations. Because of the close …
Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
P Descargues, C Deraison, C Bonnart, M Kreft… - Nature …, 2005 - nature.com
Mutations in SPINK5, encoding the serine protease inhibitor LEKTI, cause Netherton
syndrome, a severe autosomal recessive genodermatosis. Spink5−/− mice faithfully …
syndrome, a severe autosomal recessive genodermatosis. Spink5−/− mice faithfully …
[HTML][HTML] Desmoglein as a target in skin disease and beyond
M Amagai, JR Stanley - Journal of Investigative Dermatology, 2012 - Elsevier
Much of the original research on desmosomes and their biochemical components was
through analysis of skin and mucous membranes. The identification of desmogleins 1 and 3 …
through analysis of skin and mucous membranes. The identification of desmogleins 1 and 3 …
The severity of cutaneous and oral pemphigus is related to desmoglein 1 and 3 antibody levels
KE Harman, PT Seed, MJ Gratian… - British Journal of …, 2001 - academic.oup.com
Background Pemphigus vulgaris (PV) and foliaceus (PF) are characterized by antibodies to
the desmosomal proteins desmoglein 3 (Dsg3) and desmoglein 1 (Dsg1), respectively. Past …
the desmosomal proteins desmoglein 3 (Dsg3) and desmoglein 1 (Dsg1), respectively. Past …
Pemphigus vulgaris: update on etiopathogenesis, oral manifestations, and management
C Scully, SJ Challacombe - Critical Reviews in Oral Biology …, 2002 - journals.sagepub.com
Pemphigus is a group of potentially life-threatening diseases characterized by cutaneous
and mucosal blistering. There is a fairly strong genetic background to pemphigus with …
and mucosal blistering. There is a fairly strong genetic background to pemphigus with …
IgG4-positive plasma cell infiltration in the diagnosis of autoimmune pancreatitis
Autoimmune pancreatitis typically produces an enlarged pancreas with narrowing of the
pancreatic duct, and can mimic carcinoma. Autoimmune pancreatitis usually responds to …
pancreatic duct, and can mimic carcinoma. Autoimmune pancreatitis usually responds to …
Genetic and functional characterization of human pemphigus vulgaris monoclonal autoantibodies isolated by phage display
AS Payne, K Ishii, S Kacir, C Lin, H Li… - The Journal of …, 2005 - Am Soc Clin Investig
Pemphigus is a life-threatening blistering disorder of the skin and mucous membranes
caused by pathogenic autoantibodies to desmosomal adhesion proteins desmoglein 3 …
caused by pathogenic autoantibodies to desmosomal adhesion proteins desmoglein 3 …