Cell Culture/Molecular Biology core facilities were established at the time of initial finding of the SDRC to provide a resource for cultured skin cells and molecular biology technology for SDRC investigators. These cores were subsequently combined to form the Cell Culture and Molecular Technology Core. The CCMTC has four major goals by which it provides on expertise for skin specific applications on emerging gene transfer technologies, advanced instrumentations and valuable reagents. The four specific functions of the CCMTC facility are: 1. Cell Culture of various dermal and epidermal cell types A cost effective centralized source of skin-derived cells for use by core center investigators Appropriate quality measures that assure that contamination-free cultures are available An environment that fosters interactive research Provision of cell culture facilities to core center investigators Transfer of technology by """"""""hands-on"""""""" training opportunities 2. Provision of a broad base of basic molecular technologies Expertise in virus-based gene transfer technology (retroviral, adenoviral, etc.) Expertise in gene transfer systems Transfer of technology via """"""""hands-on"""""""" training """"""""Hands-on"""""""" training in molecular technologies 3. Provision of high-tech flow instrumentation and expertise in skin applications Provision of state-of-the-art analytical and cell sorting facilities 4. Provision of high-tech protein and DNA analysis instrumentation and expertise in their use for skin applications Amino acid sequencing and protein composition analysis instrumentation BIAcore protein interaction instrumentation Affymetrix Gene Array Instrumentation Automated Real Time PCR

Project Start
1988-09-30
Project End
2006-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
11
Fiscal Year
2001
Total Cost
$45,924
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Das, Lopa M; Binko, Amy M; Traylor, Zachary P et al. (2018) Defining the timing of 25(OH)D rescue following nitrogen mustard exposure. Cutan Ocul Toxicol 37:127-132
Griffith, Alexis D; Zaidi, Asifa K; Pietro, Ashley et al. (2018) A requirement for slc15a4 in imiquimod-induced systemic inflammation and psoriasiform inflammation in mice. Sci Rep 8:14451
Zaidi, Asifa K; Spaunhurst, Katrina; Sprockett, Daniel et al. (2018) Characterization of the facial microbiome in twins discordant for rosacea. Exp Dermatol 27:295-298
Bhaskaran, Natarajan; Liu, Zhihui; Saravanamuthu, Senthil S et al. (2018) Identification of Casz1 as a Regulatory Protein Controlling T Helper Cell Differentiation, Inflammation, and Immunity. Front Immunol 9:184
Mukherjee, Pranab K; Chandra, Jyotsna; Retuerto, Mauricio et al. (2018) Effect of alcohol-based hand rub on hand microbiome and hand skin health in hospitalized adult stem cell transplant patients: A pilot study. J Am Acad Dermatol 78:1218-1221.e5
Soler, David C; Young, Andrew E; Griffith, Alexis D et al. (2017) Overexpression of AQP3 and AQP10 in the skin exacerbates psoriasiform acanthosis. Exp Dermatol 26:949-951
Wang, QuanQiu; McCormick, Thomas S; Ward, Nicole L et al. (2017) Combining mechanism-based prediction with patient-based profiling for psoriasis metabolomics biomarker discovery. AMIA Annu Symp Proc 2017:1734-1743
Fritz, Yi; Klenotic, Philip A; Swindell, William R et al. (2017) Induction of Alternative Proinflammatory Cytokines Accounts for Sustained Psoriasiform Skin Inflammation in IL-17C+IL-6KO Mice. J Invest Dermatol 137:696-705
Scott, Jeffrey F; Das, Lopa M; Ahsanuddin, Sayeeda et al. (2017) Oral Vitamin D Rapidly Attenuates Inflammation from Sunburn: An Interventional Study. J Invest Dermatol 137:2078-2086
Monin, Leticia; Gudjonsson, Johann E; Childs, Erin E et al. (2017) MCPIP1/Regnase-1 Restricts IL-17A- and IL-17C-Dependent Skin Inflammation. J Immunol 198:767-775

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