The DNA Chemistry Subcore represents a merger of the previous DNA/Molecular Biology facility and a newly established DNA Sequencing facility. It is a key component of the Cell and Molecular Biology Services Core. This subcore provides synthetic DNA to DRTC and other Vanderbilt investigators and performs automated DNA sequencing. These two laboratories have been combined into a single subcore to avoid duplication of effort and to provide synergy between their complementary missions. The oligonucleotide synthesis laboratory was used by 40 DRTC investigators in 1994 to polymerize approximately 32000 bases of DNA. The oligonucleotide synthesis laboratory is also used and supported by members of the Cancer and Reproductive Biology Centers. A total of approximately 59000 bases were polymerized for all users. An oversight committee helps assure that it serves the DRTC and all of these investigators well. The DNA sequencing laboratory was established in 1994 and is jointly administered by the DRTC and the Vanderbilt Cancer Center. Its usage has grown rapidly and the resource is now operating near capacity. The two laboratories of this subcore met with high user approval in a presubmission review of our service facilities. Growth in the number of investigators who use this subcore is expected.

Project Start
2000-12-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
23
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37203
Shropshire, J Dylan; On, Jungmin; Layton, Emily M et al. (2018) One prophage WO gene rescues cytoplasmic incompatibility in Drosophila melanogaster. Proc Natl Acad Sci U S A 115:4987-4991
Lockhart, Jacob N; Spoonmore, Thomas J; McCurdy, Michael W et al. (2018) Poly(glycidol) Coating on Ultrahigh Molecular Weight Polyethylene for Reduced Biofilm Growth. ACS Appl Mater Interfaces 10:4050-4056
Schlegel, Cameron; Weis, Victoria G; Knowles, Byron C et al. (2018) Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci 63:356-365
Sucre, Jennifer M S; Deutsch, Gail H; Jetter, Christopher S et al. (2018) A Shared Pattern of ?-Catenin Activation in Bronchopulmonary Dysplasia and Idiopathic Pulmonary Fibrosis. Am J Pathol 188:853-862
Wilson, Christopher S; Chhabra, Preeti; Marshall, Andrew F et al. (2018) Healthy Donor Polyclonal IgMs Diminish B-Lymphocyte Autoreactivity, Enhance Regulatory T-Cell Generation, and Reverse Type 1 Diabetes in NOD Mice. Diabetes 67:2349-2360
Hughey, Curtis C; Trefts, Elijah; Bracy, Deanna P et al. (2018) Glycine N-methyltransferase deletion in mice diverts carbon flux from gluconeogenesis to pathways that utilize excess methionine cycle intermediates. J Biol Chem 293:11944-11954
Yao, Lina; Seaton, Sarah Craven; Ndousse-Fetter, Sula et al. (2018) A selective gut bacterial bile salt hydrolase alters host metabolism. Elife 7:
Mani, Bharath K; Castorena, Carlos M; Osborne-Lawrence, Sherri et al. (2018) Ghrelin mediates exercise endurance and the feeding response post-exercise. Mol Metab 9:114-130
Bolus, W Reid; Peterson, Kristin R; Hubler, Merla J et al. (2018) Elevating adipose eosinophils in obese mice to physiologically normal levels does not rescue metabolic impairments. Mol Metab 8:86-95
West, Kathryn L; Kelm, Nathaniel D; Carson, Robert P et al. (2018) Myelin volume fraction imaging with MRI. Neuroimage 182:511-521

Showing the most recent 10 out of 1487 publications