The Skin Diseases Research Center (SDRC), based at Case Western Reserve University (Case) and University Hospitals of Cleveland (UHC), brings added value to investigators at all the Northeast Ohio academic medical centers through its strength of focus on uniting basic and translational skin science. This successfully resulted in new diagnostics and Phase I SDRC-investigator initiated clinical trials, and there is tremendous current energy, growth, momentum, and interdisciplinary foment among the members, comprised of 86 investigators from 31 Departments, 4 schools, and 10 institutions. A major goal of the SDRC is to fuel the projects of new and experienced investigators with a rich matrix of resources in order to speed the progress and enhance the quality of skin diseases research. Proactive interactions with Pi's help focus the trajectory of our basic skin research toward translation into beneficial changes in the practice of medicine. The Case SDRC coordinates user-friendly access to state-of-the-art Core services as well as expertise in skin research techniques and their marriage to advanced institutional research resources. The Cores, together with the Pilot and Feasibility (P&F) Study and Administrative Core Programs 1) actively recruit talent to work on skin diseases, 2) promote career development of those with a skin-centered emphasis in their research, 3) advocate institutionally for applying new basic findings and technologies to skin disease applications, 4) foster communication between the members and the greater scientific and medical communities, 5) organize lecture series, symposia, retreats, and Thematic Area Working Groups, and 6) promulgate the Skinergy newsletter, the Web site, and Resident Research and Minority Student Research Programs. The P&F Study applications undergo a rigorous NIH-style of multi-level peer review. They represent a diverse array of research interests within the four Thematic Area Working Groups of the SDRC: (1) Immunology & Inflammation, (2) Photobiology & Photomedicine, (3) Infectious Disease & Host Defense, and (4) Epithelial Biology & Wound Healing. The Cores provide quality services and advanced technologies such as proteomics and imaging, ranging from basic science to clinical: A) Morphology, B) Cell Culture and Molecular Technology, C) Translational Research.and D) Animal Experimentation. This priming of research pathways greatly enhances the value and efficiency of each skin disease-related research grant.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
2P30AR039750-16
Application #
7071329
Study Section
Special Emphasis Panel (ZAR1-HL-J (J1))
Program Officer
Lapham, Cheryl K
Project Start
1997-03-01
Project End
2011-04-30
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
16
Fiscal Year
2006
Total Cost
$618,000
Indirect Cost
Name
Case Western Reserve University
Department
Dermatology
Type
Schools of Medicine
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
Swindell, William R; Sarkar, Mrinal K; Liang, Yun et al. (2017) RNA-seq identifies a diminished differentiation gene signature in primary monolayer keratinocytes grown from lesional and uninvolved psoriatic skin. Sci Rep 7:18045
Mullin, Nathaniel K; Mallipeddi, Nikhil V; Hamburg-Shields, Emily et al. (2017) Wnt/?-catenin Signaling Pathway Regulates Specific lncRNAs That Impact Dermal Fibroblasts and Skin Fibrosis. Front Genet 8:183
Arbiser, Jack L; Nowak, Ron; Michaels, Kellie et al. (2017) Evidence for biochemical barrier restoration: Topical solenopsin analogs improve inflammation and acanthosis in the KC-Tie2 mouse model of psoriasis. Sci Rep 7:11198
Larkin, Emily; Hager, Christopher; Chandra, Jyotsna et al. (2017) The Emerging Pathogen Candida auris: Growth Phenotype, Virulence Factors, Activity of Antifungals, and Effect of SCY-078, a Novel Glucan Synthesis Inhibitor, on Growth Morphology and Biofilm Formation. Antimicrob Agents Chemother 61:
Hutnick, Melanie A; Ahsanuddin, Sayeeda; Guan, Linna et al. (2017) PEGylated Dendrimers as Drug Delivery Vehicles for the Photosensitizer Silicon Phthalocyanine Pc 4 for Candidal Infections. Biomacromolecules 18:379-385

Showing the most recent 10 out of 403 publications