The Cell and Tissue Core (CTC) stimulates and supports the use of tissue culture and isolated tissues by Affiliate Investigators by consolidating several specialized activities that would not otherwise be easily accessible due to a need for special training and equipment. A practical outcome of this is that these highly specialized services are provided at uniform high yield and quality. The CTC supported 33 investigators whose projects are described in the Scientific Base of the Core section. This research covers a broad range of diabetes-related topics, from molecular biology to large, epidemiologic studies of type 1 diabetes and type 2 diabetes and diabetic complications, including: the immunology of type 1 diabetes, pancreatic islet cell biology and physiology, fuel homeostasis and obesity, diabetic dyslipidemia and cell biology of arterial wall cells, and patient-oriented medical research investigating risk factors for diabetes and its complications. Major portions of many of these projects were made possible because of the CTC. The CTC provides 1) access to tissue culture-related equipment; 2) culture medium, balanced salt solutions, and buffers; 3) cells and cell cultures from a central repository; 4) buffy coats and DNA; 5) cell transformations and transfections; 6) organ isolations and cultures; 7) technical assistance with experiments; 8) technical assistance with hybridomas; 9) training of staff and fellows in tissue culture methodology; and 10) consultation. Core administration and facilities, services, development work, training activities, and benefits are described under Core Function. Publications by investigators who have used the Core are listed in the Core Bibliography.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK017047-27
Application #
6612279
Study Section
Special Emphasis Panel (ZDK1-GRB-7 (O1))
Project Start
2002-12-01
Project End
2007-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
27
Fiscal Year
2003
Total Cost
$134,454
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Yi-Frazier, Joyce P; Cochrane, Katie; Whitlock, Kathryn et al. (2018) Trajectories of Acute Diabetes-Specific Stress in Adolescents With Type 1 Diabetes and Their Caregivers Within the First Year of Diagnosis. J Pediatr Psychol 43:645-653
Kuzma, Jessica N; Cromer, Gail; Hagman, Derek K et al. (2018) Consuming glucose-sweetened, not fructose-sweetened, beverages increases fasting insulin in healthy humans. Eur J Clin Nutr :
Basu, Debapriya; Hu, Yunying; Huggins, Lesley-Ann et al. (2018) Novel Reversible Model of Atherosclerosis and Regression Using Oligonucleotide Regulation of the LDL Receptor. Circ Res 122:560-567
Alpers, Charles E; Hudkins, Kelly L (2018) Pathology identifies glomerular treatment targets in diabetic nephropathy. Kidney Res Clin Pract 37:106-111
Campos, Carlos A; Bowen, Anna J; Roman, Carolyn W et al. (2018) Encoding of danger by parabrachial CGRP neurons. Nature 555:617-622
Kim, C; Miller, R S; Braffett, B H et al. (2018) Ovarian markers and irregular menses among women with type 1 diabetes in the Epidemiology of Diabetes Interventions and Complications study. Clin Endocrinol (Oxf) 88:453-459
Wander, Pandora L; Hayashi, Tomoshige; Sato, Kyoko Kogawa et al. (2018) Design and validation of a novel estimator of visceral adipose tissue area and comparison to existing adiposity surrogates. J Diabetes Complications 32:1062-1067
Han, Seung Jin; Fujimoto, Wilfred Y; Kahn, Steven E et al. (2018) Change in visceral adiposity is an independent predictor of future arterial pulse pressure. J Hypertens 36:299-305
Wacker, Bradley K; Dronadula, Nagadhara; Bi, Lianxiang et al. (2018) Apo A-I (Apolipoprotein A-I) Vascular Gene Therapy Provides Durable Protection Against Atherosclerosis in Hyperlipidemic Rabbits. Arterioscler Thromb Vasc Biol 38:206-217
Coleman, Brantley; Topalidou, Irini; Ailion, Michael (2018) Modulation of Gq-Rho Signaling by the ERK MAPK Pathway Controls Locomotion in Caenorhabditis elegans. Genetics 209:523-535

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