The Physiology Core is a central component of the YCCMD and critical to the success of the Center. The Core is directed by Dr. Thomas Carpenter, and is comprised of three subunits. The first of these, the Histology and Histomorphometry subunit prepares undecalcified tissue sections and performs specialized staining of bone and histomorphpmetric analyses. The second subunit, Biochemical Markers of Bone Turnover offers assays for osteocalcin, bone specific alkaline phosphatase, tartrate resistant acid phosphatase, serum, P1NP, and the C-telopeptide of type 1 collagen (CTX) as a bone resorption marker. The third subunit, Bone Densitometry and Imaging offers pQCT and, in collaboration with Dr. is currently establishing a micro-computed tomographic (uCT) facility featuring a recently acquired Scanco 35 uCT scanner. These subunits, functioning as separate but interrelated components, work synergistically to provide a comprehensive approach to analyzing a wide range of animal models. The Physiology Core has been a focal point of entry for new and junior investigators in the field, and has greatly enhanced the productivity of Center members throughout the Medical School and in the larger University research community. Core utilization has included researchers from the Departments of Internal Medicine, Orthopaedics and Rehabilitation, Pediatrics, Surgery, Obstetrics and Gynecology, Genetics, Cell Biology, Immunobiology, Biology, Comparative Medicine, and Hematology. Our training efforts have had an even broader geographic reach. This overall structure has worked well and we will maintain the described organizational format for the next funding cycle. With increased demands for services and the invariable increase in operating expenses, we have had to meet certain fiscal challenges. Our cost recovery program has allowed us to operate with a balanced budget for 9 years. Moreover, with efficient management we have maintained a sufficiently modest fee structure as to limit rate increases, thereby minimizing the impact on junior and first time investigators.
In sum, the combination of providing sophisticated technical expertise and state-of-the-art methodologies, in concert with the Core's training mission, has increased the productivity of established researchers, attracted new investigators to the field, and has increased the overall visibility of musculoskeletal research at Yale.
|Zhu, Meiling; Sun, Ben-Hua; Saar, Katarzyna et al. (2016) Deletion of Rac in Mature Osteoclasts Causes Osteopetrosis, an Age-Dependent Change in Osteoclast Number, and a Reduced Number of Osteoblasts In Vivo. J Bone Miner Res 31:864-73|
|Belinsky, Glenn S; Sreekumar, Bharath; Andrejecsk, Jillian W et al. (2016) Pigment epithelium-derived factor restoration increases bone mass and improves bone plasticity in a model of osteogenesis imperfecta type VI via Wnt3a blockade. FASEB J 30:2837-48|
|Kim, Jae Geun; Sun, Ben-Hua; Dietrich, Marcelo O et al. (2015) AgRP Neurons Regulate Bone Mass. Cell Rep 13:8-14|
|Protiva, Petr; Gong, Jingjing; Sreekumar, Bharath et al. (2015) Pigment Epithelium-Derived Factor (PEDF) Inhibits Wnt/?-catenin Signaling in the Liver. Cell Mol Gastroenterol Hepatol 1:535-549.e14|
|Wang, Meina; Nasiri, Ali R; Broadus, Arthur E et al. (2015) Periosteal PTHrP Regulates Cortical Bone Remodeling During Fracture Healing. Bone 81:104-11|
|Meijome, Tomas E; Hooker, R Adam; Cheng, Ying-Hua et al. (2015) GATA-1 deficiency rescues trabecular but not cortical bone in OPG deficient mice. J Cell Physiol 230:783-90|
|Ardeshirpour, Laleh; Dumitru, Cristina; Dann, Pamela et al. (2015) OPG Treatment Prevents Bone Loss During Lactation But Does Not Affect Milk Production or Maternal Calcium Metabolism. Endocrinology 156:2762-73|
|Yao, Chen; Yao, Gang-Qing; Sun, Ben-Hua et al. (2014) The transcription factor T-box 3 regulates colony-stimulating factor 1-dependent Jun dimerization protein 2 expression and plays an important role in osteoclastogenesis. J Biol Chem 289:6775-90|
|McCarthy, Thomas L; Yun, Zhong; Madri, Joseph A et al. (2014) Stratified control of IGF-I expression by hypoxia and stress hormones in osteoblasts. Gene 539:141-51|
|Wang, Meina; Nasiri, Ali; VanHouten, Joshua N et al. (2014) The remarkable migration of the medial collateral ligament. J Anat 224:490-8|
Showing the most recent 10 out of 127 publications