The key features of the Molecular Biology Core of the Skin Disease Research Center are its comprehensive range of services designed to support the needs of both proposed and future SDRC members, and its objective of training young investigators in the area of its expertise. This Core provides assistance in three essential areas of molecular biology central to virtually any studies ranging from the investigation of the genetic basis of human disease to cell biology experiments. These include 1) Disease-gene regulation;2) In Situ labeling of genetic alterations;and 3) Real- Time PCR, automated sequencing and cloning of DNA constructs. The core will assist center investigators in identifying the epigenetic mechanisms of a particular skin disease by promoter and mutagenesis studies and siRNA knockdown models. The Core will assist investigators in automated DNA sequence analysis to identify mutations implicated in skin disease pathogenesis and subsequent histological detection of target cells harboring these genetic mutations. The Core will also assist investigators with the design and optimization of Real-time PCR analysis for candidate disease-genes and developing a plan for ascertaining their functional consequence, and the way in which it elicits a clinical phenotype. The Core will also provide instrumentation, general resources and technical expertise in the use of automated DNA sequencing and DNA cloning. By offering these routinely used services, the Molecular Biology Core will interact closely with the other two cores. Further, the expertise offered in this Core will be almost universally utilized and provide a valuable service to most, if not all, of the Pilot and Feasibility studies, as well as other investigators within the Department.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR044535-09
Application #
8121514
Study Section
Special Emphasis Panel (ZAR1)
Project Start
Project End
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
9
Fiscal Year
2010
Total Cost
$141,933
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Shen, Yao; Stanislauskas, Milda; Li, Gen et al. (2017) Epigenetic and genetic dissections of UV-induced global gene dysregulation in skin cells through multi-omics analyses. Sci Rep 7:42646
Mathew, Grinu; Hannan, Abdul; Hertzler-Schaefer, Kristina et al. (2016) Targeting of Ras-mediated FGF signaling suppresses Pten-deficient skin tumor. Proc Natl Acad Sci U S A 113:13156-13161
Shen, Yao; Kim, Arianna L; Du, Rong et al. (2016) Transcriptome Analysis Identifies the Dysregulation of Ultraviolet Target Genes in Human Skin Cancers. PLoS One 11:e0163054
Dai, Zhenpeng; Xing, Luzhou; Cerise, Jane et al. (2016) CXCR3 Blockade Inhibits T Cell Migration into the Skin and Prevents Development of Alopecia Areata. J Immunol 197:1089-99
Abaci, Hasan E; Guo, Zongyou; Coffman, Abigail et al. (2016) Human Skin Constructs with Spatially Controlled Vasculature Using Primary and iPSC-Derived Endothelial Cells. Adv Healthc Mater 5:1800-7
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
Johnson, Dylan; Mathur, Mohit C; Kobayashi, Tomoyoshi et al. (2016) The Cardiomyopathy Mutation, R146G Troponin I, Stabilizes the Intermediate ""C"" State of Regulated Actin under High- and Low-Free Ca(2+) Conditions. Biochemistry 55:4533-40
Shinkuma, Satoru; Guo, Zongyou; Christiano, Angela M (2016) Site-specific genome editing for correction of induced pluripotent stem cells derived from dominant dystrophic epidermolysis bullosa. Proc Natl Acad Sci U S A 113:5676-81
Kim, Arianna L; Back, Jung Ho; Zhu, Yucui et al. (2016) AKT1 Activation is Obligatory for Spontaneous BCC Tumor Growth in a Murine Model that Mimics Some Features of Basal Cell Nevus Syndrome. Cancer Prev Res (Phila) 9:794-802
Sun, Xiaoyun; Kim, Arianna; Nakatani, Masashi et al. (2016) Distinctive molecular responses to ultraviolet radiation between keratinocytes and melanocytes. Exp Dermatol 25:708-13

Showing the most recent 10 out of 130 publications