The Northeast Ohio Skin Diseases (SDRC) at Case Western Reserve University (CWRU) was originally funded under Dr. D. Bickers from 88- 93, then under Dr. C. Elements from 93-97, and finally Dr. K. Cooper became the director. Since 199 it has operated under a no-cost extension and institutional bridge funds, and has continued to grow and expand services. This revised application builds upon a tremendous skin research base and outstanding productivity, combined with the energized and fresh initiatives of a new director and a great influx of new faculty to the Department of Dermatology and CWRU. CWRU is an institution renowned for its environment conductive to innovative interdisciplinary approaches to biomedical research and education. The SDRC at CWRU promotes cooperative education among investigators engaged directly in skin diseases research with those conducting state-of-the-art biomedical research in other disciplines that have relevance to skin disease. Comprised of 64 talented investigators from 17 different departments with over $25 million on annual support in skin-related national research funding ($1.7 million of which is form NIAMS), the Center has greatly leveraged the SDRC investment over 7 fold through advocacy of skin diseases research and fostering excellence in dermatological research. New initiatives for the next funding cycle include: (1) to translate innovative basic research to patients with skin disease, and (2) facilitate the development of young investigators into fully independent researchers in skin disease-related research, (3) provide a vibrant milieu for maximum cooperating among skin researchers, and (4) bring together precious resources to expedite skin research. The SDRC will encompass four Core facilities: (1) Molecular and Cellular Morphology, (2) Cell Culture and Molecular Technology, (3) Translational Research, and (4) Animal Experimentation. These Cores will provide skin specific expertise in technological services, training and consultation to SDRC members and to investigators directing the Pilot and Feasibility Studies. he studies highlight interactions among the four thematic research areas of the SDRC: (A) Immunology/Microbiology, (b) Photocarcinogenesis/Photobiology/Photomedicine, (c) Oncology, and (d) Cell Biology. A highly effective Administrative Core and Enrichment Program that is already in place maximizes cooperate interaction at all levels. The ultimate goal of this Core and Enrichment Program that is already in place maximizes cooperative interaction at all levels. The ultimate goal of this SDRC is to generate new knowledge that will have a sustained impact on cutaneous biology and that will improve the quality of life of patients with skin disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR039750-12
Application #
6511694
Study Section
Special Emphasis Panel (ZAR1-AAA-A (J3))
Program Officer
Freeman, Julia B
Project Start
1988-09-30
Project End
2006-04-30
Budget Start
2002-05-01
Budget End
2003-04-30
Support Year
12
Fiscal Year
2002
Total Cost
$606,403
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
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
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
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