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pro vyhledávání: '"Z. Kaymakcalan"'
Autor:
Z. Kaymakcalan, Yonghao Cao, D M Conlon, L Sidur, F Hong, Carolyn A. Cuff, Y Fang, Melanie C. Ruzek, Kristine M. Smith
Publikováno v:
British Journal of Dermatology. 185:804-814
Background Adalimumab provides significant efficacy for patients with hidradenitis suppurativa (HS), which was demonstrated by at least 50% of patients achieving a clinical response by week 12 that was maintained through to week 168 in the PIONEER tr
Publikováno v:
Journal of Investigative Dermatology. 142:S131
Autor:
Jing Wang, Bohdan P. Harvey, Erin Murphy, Z. Kaymakcalan, Yonghao Cao, Feng Hong, Melanie Ruzek
Publikováno v:
The Journal of investigative dermatology. 141(11)
Adalimumab (ADA) is the only Food and Drug Administration‒approved treatment for moderate-to-severe hidradenitis suppurativa, whereas etanercept and certolizumab-pegol have been shown to be ineffective, suggesting that the mechanism of action of AD
Akademický článek
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Autor:
Bohdan P. Harvey, Z. Kaymakcalan
Publikováno v:
Poster Presentations.
Background: Therapeutic anti-TNF biologic agents can be distinct in their structure, such as etanercept, a human TNFRII- Fc fusion protein, as compared to adalimumab, a human IgG molecule, and/or in their binding to TNF as shown by crystal structures
Publikováno v:
Saturday, 16 JUNE 2018.
Background TNF-alpha (TNFa) has been shown to contribute to osteoclastogenesis (OCgenesis) independently and in conjunction with M-CSF or RANKL, two key cytokines involved in osteoclast (OC) development. We have previously demonstrated that TNF enhan
Publikováno v:
Poster Presentations.
Background The CXCL12/CXCR4 chemokine axis has been implicated in the pathogenesis of RA. The expression of this chemokine and receptor has been shown to be increased in RA synovium, and moreover, CXCR4 levels in synovium have been correlated with jo
Publikováno v:
Journal of Investigative Dermatology. 139:S161
Publikováno v:
Analytical Biochemistry. 299:119-129
The binding of fully human monoclonal antibodies (MAbs) D2E7 and 2SD4 to their antigen, human tumor necrosis factor-alpha (TNFalpha), was investigated by BIAcore, cation exchange (CIEX), and size exclusion liquid chromatography (SEC) using ultraviole
Publikováno v:
Annals of the Rheumatic Diseases. 75:918.2-918
Background TNF has been shown to contribute to osteoclastogenesis independently and in conjunction with M-CSF or RANKL, two key cytokines involved in osteoclast (OC) development. We have previously demonstrated that TNF enhances the kinetics of RANKL