Core A is the Administrative Core forthe Phase III COBRE: Smooth Muscle Plasticity. COBRE programs are complicated by the fact that several moving parts must be coordinated to accomplish the goals ofthe program. The main goal of this Phase III is to support the services of 2 scientific Core facilities that are essential to the funded research of the smooth muscle biology group at UNR. Several projects would be serverly limited by loss of function of the FACS and Flow Cytometry Core and the Single Cell Molecular Expression Core (Core B&C ofthe Phase III COBRE). Thus, sustaining the function and quality of these Cores is paramount to retention and growth ofthe Research Base in the COBRE thematic focus. We will also conduct a Pilot Grant Program that will allow many other research projects within the University and potentially within the State of Nevada to benefit from Core technologies. We will also partner with other IDeA programs at UNR to extend the functions of the Core laboratories and share personnel and expertise. Core A will lead the Phase III by seeking to achieve the following specific aims, i) Build and secure Core technologies and excellence of service. Use Phase III to leverage University, State and commercial resources to further enhance Core utilization, technology and service, ii) Insure Core sustainability through enhancement of utilization and quality of services, iii) Maintain vibrant and effective mentoring of junior faculty to help them obtain extramural funding and augment career potential. Build technical capabilities of junior faculty by providing access to Cores through the Pilot Grant Program, iv) Provide regular evaluation of Phase III activities and services. Integrate assessments from users, Core directors. Internal Steering Committee, and External Advisory Committee. Develop Action Plans based on evaluations to remedy less than optimal performance and/or service, v) Provide all required reporting for Phase III activities to maintain compliance with University, State and Federal regulations. The Smooth Muscle Plasticity COBRE at UNR has had many scientific and career development successes since it inception. Core A will maintain the trajectory of success in the Phase III, creating dynamic, sustainable scientific Cores for UNR.

Public Health Relevance

Core A will administrate the Phase III ofthe Center of Biomedical Research Excellence: Smooth muscle plasticity at the University of Nevada. Phase III will develop and make sustainable 2 scientific cores essential to the further development of the thematic focus of the center. Core A will also oversee a Pilot Research Program designed to help other investigators develop expertise and pilot data using the Cores.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Center Core Grants (P30)
Project #
1P30GM110767-01
Application #
8735444
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Nevada Reno
Department
Type
DUNS #
City
Reno
State
NV
Country
United States
Zip Code
89557
Wang, Zhuqing; Lee, Sandy; Oliver, Daniel et al. (2018) Prps1l1, a testis-specific gene, is dispensable for mouse spermatogenesis. Mol Reprod Dev 85:802-804
Shi, Junchao; Ko, Eun-A; Sanders, Kenton M et al. (2018) SPORTS1.0: A Tool for Annotating and Profiling Non-coding RNAs Optimized for rRNA- and tRNA-derived Small RNAs. Genomics Proteomics Bioinformatics 16:144-151
Blanco, Luz P; Payne, Bryan L; Feyertag, Felix et al. (2018) Proteins of generalist and specialist pathogens differ in their amino acid composition. Life Sci Alliance 1:e201800017
Ben Maamar, Millissia; Sadler-Riggleman, Ingrid; Beck, Daniel et al. (2018) Alterations in sperm DNA methylation, non-coding RNA expression, and histone retention mediate vinclozolin-induced epigenetic transgenerational inheritance of disease. Environ Epigenet 4:dvy010
Zhang, Yunfang; Zhang, Xudong; Shi, Junchao et al. (2018) Dnmt2 mediates intergenerational transmission of paternally acquired metabolic disorders through sperm small non-coding RNAs. Nat Cell Biol 20:535-540
Tang, Chong; Klukovich, Rachel; Peng, Hongying et al. (2018) ALKBH5-dependent m6A demethylation controls splicing and stability of long 3'-UTR mRNAs in male germ cells. Proc Natl Acad Sci U S A 115:E325-E333
Skinner, Michael K; Ben Maamar, Millissia; Sadler-Riggleman, Ingrid et al. (2018) Alterations in sperm DNA methylation, non-coding RNA and histone retention associate with DDT-induced epigenetic transgenerational inheritance of disease. Epigenetics Chromatin 11:8
Singh, Mahendra; Miura, Pedro; Renden, Robert (2018) Age-related defects in short-term plasticity are reversed by acetyl-L-carnitine at the mouse calyx of Held. Neurobiol Aging 67:108-119
Baker, Salah A; Drumm, Bernard T; Skowronek, Karolina E et al. (2018) Excitatory Neuronal Responses of Ca2+ Transients in Interstitial Cells of Cajal in the Small Intestine. eNeuro 5:
Heredia, Dante J; Feng, Cheng-Yuan; Agarwal, Andrea et al. (2018) Postnatal Restriction of Activity-Induced Ca2+ Responses to Schwann Cells at the Neuromuscular Junction Are Caused by the Proximo-Distal Loss of Axonal Synaptic Vesicles during Development. J Neurosci 38:8650-8665

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