Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Mong Shang Lin"'
Publikováno v:
Journal of Biological Chemistry. 294:6227-6239
Gcn5 and sirtuins are highly conserved histone acetyltransferase (HAT) and histone deacetylase (HDAC) enzymes that were first characterized as regulators of gene expression. Although histone tails are important substrates of these enzymes, they also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46ed443472740d2eac5cee2855316bba
https://doi.org/10.1074/jbc.ra118.006051
https://doi.org/10.1074/jbc.ra118.006051
Gcn5 and sirtuins are highly conserved HAT and HDAC enzymes that were first characterised as regulators of gene expression. Although histone tails are important substrates of these enzymes, these proteins also target many non-histone substrates that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ff9a249246f77d8c993050e3dcf4fb
Autor:
Mukesh Kumar, Kailash C. Bhol, Mong-Shang Lin, Lisa A. Cavacini, Shih-Wei Yeh, Mark Duval, Marshall R. Posner, A. Razzaque Ahmed
Publikováno v:
Clinical Immunology. 120:68-75
Pemphigus vulgaris (PV) is a potentially fatal autoimmune mucocutaneous disease associated with production of IgG autoantibodies to desmoglein 3 (Dsg3), a 130-kDa epidermal cadherin protein. The binding of pathogenic antibody to Dsg3 on epidermal ker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ff6e9a833d7e89572582ed0844d9de8
https://doi.org/10.1016/j.clim.2006.03.006
https://doi.org/10.1016/j.clim.2006.03.006
Publikováno v:
Clinical Immunology. 116:54-64
Pemphigus vulgaris (PV) is an acquired immunobullous disorder. At the early stage of the disease (mucosal PV), patients display only autoimmunity to desmoglein (Dsg) 3 and develop mucosal blisters; while at the later stage of the disease (mucocutaneo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f814f440e9c9790ff8489f7e8a05aa84
https://doi.org/10.1016/j.clim.2005.03.005
https://doi.org/10.1016/j.clim.2005.03.005
Publikováno v:
Journal of the American Academy of Dermatology. 51:118-122
Bullous pemphigoid (BP) and epidermolysis bullosa acquisita are distinct autoimmune blistering disorders. BP is characterized by autoantibodies directed against the NC16A domain of collagen XVII, whereas patients with epidermolysis bullosa acquisita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aa1c89cbeec042982718994c6a78f1b
https://doi.org/10.1016/j.jaad.2003.12.033
https://doi.org/10.1016/j.jaad.2003.12.033
Publikováno v:
Journal of Investigative Dermatology. 121:1373-1378
Pemphigus foliaceus (PF) is an antibody-mediated autoimmune disorder with IgG1 and IgG4 as the predominant subclasses of autoantibodies against a desmosomal glycoprotein, desmoglein-1 (Dsg1). Previously, we found that the IgG4 anti-Dsg1 autoantibodie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2430c1ffe300e9dfa8555146963e8032
https://doi.org/10.1111/j.1523-1747.2003.12608.x
https://doi.org/10.1111/j.1523-1747.2003.12608.x
Autor:
G. J. Giudice, Mong Shang Lin, Bahjat F. Qaqish, Luis A. Arteaga, Gunter Hans-Filho, Valeria Aoki, Simon Warren, Evandro A. Rivitti, Luis A. Diaz
Publikováno v:
Journal of Investigative Dermatology. 120:1-5
Endemic pemphigus foliaceus, like the sporadic form seen in the developed world, is mediated by IgG antibodies to desmoglein-1. We studied an endemic focus in Limao Verde, Brazil, where disease prevalence is 3.4%. We previously detected IgG antibodie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0606bd24c901fbff4c416191c9eb21b2
https://doi.org/10.1046/j.1523-1747.2003.12017.x
https://doi.org/10.1046/j.1523-1747.2003.12017.x
Publikováno v:
Clinical Immunology. 105:64-74
In this study we systematically characterized isotype profiles and antigenic and tissue specificity of antidesmoglein autoantibodies from patients with pemphigus foliaceus (PF) and pemphigus vulgaris (PV) using enzyme-linked immunoabsorbent assays (E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f194c98cf121983d2efa673b1c8e0782
https://doi.org/10.1006/clim.2002.5259
https://doi.org/10.1006/clim.2002.5259
Autor:
Janet A. Fairley, Detlef Zillikens, Monica Olague-Marchan, Chang-Ling Fu, George J. Giudice, Mary K. Hacker, Mong-Shang Lin
Publikováno v:
Clinical Immunology. 102:310-319
Linear IgA bullous disease (LABD) is an autoimmune skin disease characterized by subepidermal blisters and IgA autoantibodies directed against the epidermal basement membrane zone (BMZ) of the skin. Various antigens have been identified as targets of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5716a3eeb6403c36d641e212206db0a3
https://doi.org/10.1006/clim.2001.5177
https://doi.org/10.1006/clim.2001.5177
Autor:
Raymond G. Hoffmann, Luis A. Diaz, Simon Warren, Mong Shang Lin, Evandro A. Rivitti, George J. Giudice, Gunter Hans-Filho, Vandir dos Santos, Valeria Aoki
Publikováno v:
New England Journal of Medicine. 343:23-30
Background Pemphigus foliaceus is an autoimmune skin disease mediated by autoantibodies against desmoglein 1. The endemic form is thought to have an environmental cause. The Terena reservation of Limao Verde in Mato Grosso do Sul, Brazil, is a recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794ff99d9b03c1486d042a8f9e9e6420
https://doi.org/10.1056/nejm200007063430104
https://doi.org/10.1056/nejm200007063430104