This application requests funding for the establishment of the Yale Skin Disease Research Core Center (YSDRC), which will bring together a collaborative, multidisciplinary group of 25 independent Investigators (as well as 19 other Associate Investigators and Consultants) based in the departments/divisions of Dermatology, Biology, Cardiobiology, Comparative Medicine, Endocrinology, Human Genetics, Immunobiology, Molecular Biophysics and Biochemistry, Oncology, Pathology, Pediatrics, Pharmacology, Plastic Surgery, Pulmonary Medicine, and Therapeutic Radiology, all sharing a commitment to advancing understanding of the etiology and pathogenesis of skin diseases through investigation of both the normal and pathologic structure and function of skin. YSDRC research activities will center around three major themes: T cell lymphoma and physiologic T cell:skin interactions; the biology of melanocytes and melanoma; and the growth and differentiation of normal and malignant keratinocytes. Three Core units, each interacting with other Yale resource facilities will be established: Molecular Analysis; Cell Culture; and Tissue Acquisition and Distribution/Biological Structure and Function. The YSDRC pilot/feasibility program will enhance the development of new interdisciplinary skin-related investigation by requiring that projects involve substantive collaboration between investigators with complementary interests. The YSDRC enrichment program provides multiple opportunities to develop new national as well as institutional collaborative studies. These facilities/programs will thus each contribute to achieving the YSDRC's principal goal of creating an environment which will greatly amplify our understanding of basic cutaneous biology as well as of a broad variety of skin diseases. To achieve that goal, the specific aims of the YSDRC are to: 1) stimulate new multidisciplinary interactions; 2) stimulate new investigators to become involved in one or more areas of YSDRC research; 3) capitalize on potentially important new research opportunities through interdisciplinary pilot/feasibility projects; 4) organize time-consuming, expensive techniques and procedures into cost-efficient core facilities used by multiple investigators; 5) provide a rich training environment; and 6) foster national and international collaborations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR041942-07
Application #
6171295
Study Section
Special Emphasis Panel (ZAR1-AAA-C (J1))
Program Officer
Lapham, Cheryl K
Project Start
1992-09-30
Project End
2004-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
7
Fiscal Year
2000
Total Cost
$650,333
Indirect Cost
Name
Yale University
Department
Dermatology
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Dainichi, Teruki; Hayden, Matthew S; Park, Sung-Gyoo et al. (2016) PDK1 Is a Regulator of Epidermal Differentiation that Activates and Organizes Asymmetric Cell Division. Cell Rep 15:1615-23
Askenase, Phillip W; Bryniarski, Krzysztof; Paliwal, Vipin et al. (2015) A subset of AID-dependent B-1a cells initiates hypersensitivity and pneumococcal pneumonia resistance. Ann N Y Acad Sci 1362:200-14
Clark, Paul R; Jensen, Todd J; Kluger, Martin S et al. (2011) MEK5 is activated by shear stress, activates ERK5 and induces KLF4 to modulate TNF responses in human dermal microvascular endothelial cells. Microcirculation 18:102-17
Kwong, Bernice Y; Roberts, Scott J; Silberzahn, Tobias et al. (2010) Molecular analysis of tumor-promoting CD8+ T cells in two-stage cutaneous chemical carcinogenesis. J Invest Dermatol 130:1726-36
Radtke, Christine; Vogt, Peter M; Devor, Marshall et al. (2010) Keratinocytes acting on injured afferents induce extreme neuronal hyperexcitability and chronic pain. Pain 148:94-102
Kirkiles-Smith, Nancy C; Harding, Martha J; Shepherd, Benjamin R et al. (2009) Development of a humanized mouse model to study the role of macrophages in allograft injury. Transplantation 87:189-97
Koga, Yasuo; Pelizzola, Mattia; Cheng, Elaine et al. (2009) Genome-wide screen of promoter methylation identifies novel markers in melanoma. Genome Res 19:1462-70
Yates, Kristin E; Korbel, Gregory A; Shtutman, Michael et al. (2008) Repression of the SUMO-specific protease Senp1 induces p53-dependent premature senescence in normal human fibroblasts. Aging Cell 7:609-21
Pelizzola, Mattia; Koga, Yasuo; Urban, Alexander Eckehart et al. (2008) MEDME: an experimental and analytical methodology for the estimation of DNA methylation levels based on microarray derived MeDIP-enrichment. Genome Res 18:1652-9
Shen, Xiaoyan; Berger, Carole L; Tigelaar, Robert et al. (2008) Development of immunogenic tumor-loaded dendritic cells through physical perturbation and apoptotic cell loading. Immunol Invest 37:798-821

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