The Animal Research Core will provide investigators of each project with assistance in the conduct of research involving mice. To do this, the core will perform the following: 1. Maintain mouse breeding colonies and a database containing relevant information. Data on strain designation, genotype, date of birth, identity of parents, cage card number, sex, number in cage, transponder identification number, and other information as needed will be entered and maintained in a computerized database. Updated information on each breeding colony will be provided to investigators on a weekly basis. Core personnel will be responsible for daily monitoring of each breeder colony, weaning of littermates, implantation of transponders, and setting up an appropriate number of breeder cages. 2.Genotyping of transgenic and mutant mice. Tail DNA will be isolated and used to perform PCR to determine the genotype of founder transgenic and knockout mice obtained by project investigators from commercial sources or from collaborators, and of animals produced by breeding colonies. 3. Assist in the conduct of animal experiments. Core personnel will coordinate and assist in the performance of standardized procedures during the conduct of animal experiments by investigators in each project. These procedures include implantation of transponders and recording of identification numbers, administration of test substances, obtained serum samples, and killing animals before tissue harvest.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG013918-07
Application #
6596376
Study Section
Special Emphasis Panel (ZAG1)
Project Start
2002-06-15
Project End
2003-05-31
Budget Start
Budget End
Support Year
7
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Type
DUNS #
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Farr, Joshua N; Almeida, Maria (2018) The Spectrum of Fundamental Basic Science Discoveries Contributing to Organismal Aging. J Bone Miner Res 33:1568-1584
Weinstein, Robert S; Hogan, Erin A; Borrelli, Michael J et al. (2017) The Pathophysiological Sequence of Glucocorticoid-Induced Osteonecrosis of the Femoral Head in Male Mice. Endocrinology 158:3817-3831
Kim, Ha-Neui; Chang, Jianhui; Shao, Lijian et al. (2017) DNA damage and senescence in osteoprogenitors expressing Osx1 may cause their decrease with age. Aging Cell 16:693-703
Ucer, Serra; Iyer, Srividhya; Kim, Ha-Neui et al. (2017) The Effects of Aging and Sex Steroid Deficiency on the Murine Skeleton Are Independent and Mechanistically Distinct. J Bone Miner Res 32:560-574
Iyer, Srividhya; Han, Li; Ambrogini, Elena et al. (2017) Deletion of FoxO1, 3, and 4 in Osteoblast Progenitors Attenuates the Loss of Cancellous Bone Mass in a Mouse Model of Type 1 Diabetes. J Bone Miner Res 32:60-69
Almeida, Maria; Laurent, Michaƫl R; Dubois, Vanessa et al. (2017) Estrogens and Androgens in Skeletal Physiology and Pathophysiology. Physiol Rev 97:135-187
Piemontese, Marilina; Almeida, Maria; Robling, Alexander G et al. (2017) Old age causes de novo intracortical bone remodeling and porosity in mice. JCI Insight 2:
Piemontese, Marilina; Xiong, Jinhu; Fujiwara, Yuko et al. (2016) Cortical bone loss caused by glucocorticoid excess requires RANKL production by osteocytes and is associated with reduced OPG expression in mice. Am J Physiol Endocrinol Metab 311:E587-93
Fujiwara, Toshifumi; Ye, Shiqiao; Castro-Gomes, Thiago et al. (2016) PLEKHM1/DEF8/RAB7 complex regulates lysosome positioning and bone homeostasis. JCI Insight 1:e86330
Fujiwara, T; Zhou, J; Ye, S et al. (2016) RNA-binding protein Musashi2 induced by RANKL is critical for osteoclast survival. Cell Death Dis 7:e2300

Showing the most recent 10 out of 162 publications