Zobrazeno 1 - 10
of 99
pro vyhledávání: '"George J. Giudice"'
Autor:
Kelly A.N. Messingham, George J. Giudice, Elizabeth M. Vanderah, Amber Onoh, Janet A. Fairley
Publikováno v:
Hybridoma. 31:111-117
BP180 (collagen XVII) is the target antigen in several autoimmune diseases including bullous pemphigoid (BP). Both IgE and IgG class autoantibodies have been shown to be pathogenic in BP; however, studies designed to elucidate the patho-mechanisms me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8230b90e4628eadd70a4d28efde68df
https://doi.org/10.1089/hyb.2011.0102
https://doi.org/10.1089/hyb.2011.0102
Publikováno v:
Journal of Immunological Methods. 346:18-25
Bullous pemphigoid (BP) is a humoral autoimmune disease directed predominantly against the non-collagenous NC16A domain of the BP180 hemidesmosomal protein. Our laboratory has recently shown, using a mouse xenograft model, that passive transfer of Ig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa375037444ea5fce2992893a3520e9
https://doi.org/10.1016/j.jim.2009.04.013
https://doi.org/10.1016/j.jim.2009.04.013
Autor:
Randy J. Thresher, Zhi Liu, George J. Giudice, Gang Ning, Wen Sui, Minglang Zhao, Zhuowei Li, Ning Li, Cassian Sitaru, Detlef Zillikens, Luis A. Diaz, Janet A. Fairley, M. Peter Marinkovich
Publikováno v:
Journal of Autoimmunity. 31:331-338
Bullous pemphigoid (BP) is a cutaneous autoimmune inflammatory disease associated with subepidermal blistering and autoantibodies against BP180, a transmembrane collagen and major component of the hemidesmosome. Numerous inflammatory cells infiltrate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc785f6de9e367eec8ccb88712fded96
https://doi.org/10.1016/j.jaut.2008.08.009
https://doi.org/10.1016/j.jaut.2008.08.009
Publikováno v:
Journal of Investigative Dermatology. 125(3):467-472
Bullous pemphigoid (BP) is a subepidermal blistering disease characterized by autoantibodies against the hemidesmosomal protein BP180 (BPAg2, type XVII collagen). NC16A, a non-collagenous stretch of the BP180 ectodomain, is the primary target of path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494f02fb7b7ad054d178c2bde9734ba2
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
Autor:
Francoise Van den Bergh, Otobia G. Dimson, Marleen M. Janson, Simon Warren, George J. Giudice, Chang Ling Fu, Janet A. Fairley
Publikováno v:
Journal of Investigative Dermatology. 120:784-788
Bullous pemphigoid (BP) is an autoimmune skin disease characterized by autoantibodies against the hemidesmosomal protein BP180. In addition to IgG autoantibodies, IgE class autoantibodies have been reported in BP patients. Because animal models utili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5655f27d681e19064e5ca346e284eb0
https://doi.org/10.1046/j.1523-1747.2003.12146.x
https://doi.org/10.1046/j.1523-1747.2003.12146.x
Autor:
Ming Lang Zhao, Ruoyan Chen, Zhi Liu, George J. Giudice, Janet A. Fairley, Detlef Zillikens, Luis A. Diaz
Publikováno v:
The Journal of Immunology. 169:3987-3992
Bullous pemphigoid (BP) is a subepidermal blistering disease associated with autoantibodies against two hemidesmosomal proteins, BP180 and BP230. Numerous inflammatory cells infiltrate the upper dermis in BP. We have previously shown by passive trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e61d82748b3f78061845bca521ccf875
https://doi.org/10.4049/jimmunol.169.7.3987
https://doi.org/10.4049/jimmunol.169.7.3987
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
Autor:
Sally S. Twining, Mary K. Hacker, George J. Giudice, Monica Olague-Marchan, Luis A. Diaz, John A. McGrath
Publikováno v:
Matrix Biology. 19:223-233
BP180 is a homotrimeric transmembrane protein with a carboxy-terminal ectodomain that forms an interrupted collagen triple helix. Null type mutations in the BP180 gene produce a recessive subepidermal blistering disease, non-Herlitz junctional epider
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b0168c92e4b414a1ebeaaf19088595
https://doi.org/10.1016/s0945-053x(00)00070-6
https://doi.org/10.1016/s0945-053x(00)00070-6