3 results match your criteria: "J.L. Pettis VA Medical Center and Loma Linda University[Affiliation]"
Bone
May 2003
Molecular Genetics Division, Musculoskeletal Disease Center, J.L. Pettis VA Medical Center and Loma Linda University, Loma Linda, CA 92357, USA.
To test the hypothesis that periosteal circumference (PC), which is associated with bone size through cross-sectional moment of inertia (CMI), has heritable components, we performed a linkage analysis using 633 MRL/SJL F(2) mice that have 14% difference in mean PC. PC was determined in femurs by use of peripheral quantitative computerized tomography (pQCT). The genome-wide scan identified nine QTL for PC adjusted by body weight on chromosomes 1 (2 QTL), 2 (2 QTL), 8, 11, 15, 17, and X, which accounted for 38.
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August 2002
Molecular Genetics Division, Musculoskeletal Disease Center, J.L. Pettis VA Medical Center and Loma Linda University, 11201 Benton Street (151), CA 92357, USA.
Studies on the genetic mechanisms involved in the regulation of lean body mass (LBM) in mammals are minimal, although LBM is associated with a competent immune system and an overall good (healthy) body functional status. In this study, we performed a high-density genome-wide scan using 633 (MRL/MPJ x SJL/J) F(2) intercross to identify the quantitative trait loci (QTL) involved in the regulation of LBM. We hypothesized that additional QTL can be identified using a different mouse cross (MRL/SJL cross).
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August 2001
Molecular Genetics Division, Musculoskeletal Disease Center, J. L. Pettis VA Medical Center and Loma Linda University, Loma Linda, CA 92357, USA.
Genetic variation in bone-regenerative capacity has not been studied in any animal model system. We developed a "drill-hole" model in the tail vertebra of inbred strains of mice that allows us to reproducibly introduce an injury with a defined boundary and quantify the rate of bone healing using the combination of high-resolution Faxitron X-ray imaging and the ChemiImager 4000 Low Light Imaging System. Using this model, we demonstrate that bone-regenerative capacity is a genetically controlled trait with an estimated heritability of 72%, and that it differs significantly among inbred strains of mice.
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