This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Over this year-3 of phase-II Center development, Core A has continued to serve effectively to: steer scientifically thematic program and faculty development;deliver focused mentoring; guide resource utilization; provide national interactions and career development opportunities;and to further build our Center via the successful recruitment of outstanding new junior and senior faculty. Internal and External Advisory Committees (IAC, EAC) continue to provide critical input on research projects for merit, impact, clinical relevance, and progress. Mentoring on projects, grant proposals, publications, and career development also occurs via direct investigator-mentor pairings, and this is reinforced via IAC and EAC activities. Decisions on faculty recruitment, hires, and possible advancement are further influenced via this core, and its constituents. Core A and its defined components also interact with clinical and educational arms of our parent medical center, and with our Institute's external scientific advisory board. These interactions likewise bolster career development. Overall, Core A has evolved to comprise an important and quite productive hub. Core A also has continued to contribute sponsorship for a robust invited seminar series, as well as new joint sponsorship of an outstanding Summer Symposium in Stem Cell Biology (with the Jackson Laboratory and MDIBL).

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR018789-09
Application #
8360261
Study Section
Special Emphasis Panel (ZRR1-RI-6 (01))
Project Start
2011-06-01
Project End
2012-05-31
Budget Start
2011-06-01
Budget End
2012-05-31
Support Year
9
Fiscal Year
2011
Total Cost
$233,644
Indirect Cost
Name
Maine Medical Center
Department
Type
DUNS #
071732663
City
Portland
State
ME
Country
United States
Zip Code
04102
Duarte, Christine W; Black, Adam W; Lucas, F Lee et al. (2017) Cancer incidence in patients with hereditary hemorrhagic telangiectasia. J Cancer Res Clin Oncol 143:209-214
Caron, Jennifer M; Ames, Jacquelyn J; Contois, Liangru et al. (2016) Inhibition of Ovarian Tumor Growth by Targeting the HU177 Cryptic Collagen Epitope. Am J Pathol 186:1649-61
Stohn, J Patrizia; Wang, Qiaozeng; Siviski, Matthew E et al. (2015) Cthrc1 controls adipose tissue formation, body composition, and physical activity. Obesity (Silver Spring) 23:1633-42
Ufkin, Melanie L; Peterson, Sarah; Yang, Xuehui et al. (2014) miR-125a regulates cell cycle, proliferation, and apoptosis by targeting the ErbB pathway in acute myeloid leukemia. Leuk Res 38:402-10
He, Qing; Yang, Xuehui; Gong, Yan et al. (2014) Deficiency of Sef is associated with increased postnatal cortical bone mass by regulating Runx2 activity. J Bone Miner Res 29:1217-31
Motyl, Katherine J; Bishop, Kathleen A; DeMambro, Victoria E et al. (2013) Altered thermogenesis and impaired bone remodeling in Misty mice. J Bone Miner Res 28:1885-97
Hasham, Muneer G; Snow, Kathy J; Donghia, Nina M et al. (2012) Activation-induced cytidine deaminase-initiated off-target DNA breaks are detected and resolved during S phase. J Immunol 189:2374-82
Singh, Seema; Dev, Arvind; Verma, Rakesh et al. (2012) Defining an EPOR- regulated transcriptome for primary progenitors, including Tnfr-sf13c as a novel mediator of EPO- dependent erythroblast formation. PLoS One 7:e38530
Apra, Caroline; Richard, Laurence; Coulpier, Fanny et al. (2012) Cthrc1 is a negative regulator of myelination in Schwann cells. Glia 60:393-403
Krebs, Luke T; Bradley, Cara K; Norton, Christine R et al. (2012) The Notch-regulated ankyrin repeat protein is required for proper anterior-posterior somite patterning in mice. Genesis 50:366-74

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