The human skeleton is affected by mutations in low-density lipoprotein receptor-related protein 5 (LRP5). To understand how LRP5 influences bone properties, we generated mice with osteocyte-specific expression of inducible Lrp5 mutations that cause high and low bone mass phenotypes in humans. We found that bone properties in these mice were comparable to bone properties in mice with inherited mutations. We also induced an Lrp5 mutation in cells that form the appendicular skeleton but not in cells that form the axial skeleton; we observed that bone properties were altered in the limb but not in the spine. These data indicate that Lrp5 signaling functions locally, and they suggest that increasing LRP5 signaling in mature bone cells may be a s...
PURPOSE OF REVIEW: This review summarizes recent findings concerning the genomic variations of the l...
Skeletal health relies on architectural integrity and sufficient bone mass, which are maintained thr...
BACKGROUND: Primary osteoporosis is a rare childhood-onset skeletal condition whose pathogenesis has...
The human skeleton is affected by mutations in Low-density lipoprotein Receptor-related Protein 5 (L...
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, en...
Genetic studies in humans have shown loss-of-function mutations in the LRP5 gene to be responsible f...
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, en...
AbstractIn humans, low peak bone mass is a significant risk factor for osteoporosis. We report that ...
The low density lipoprotein receptor-related protein-5 (LRP5) is a Wnt co-receptor that has been sho...
The low density lipoprotein receptor-related protein-5 (LRP5), a co-receptor in the Wnt signaling pa...
AbstractIntroductionTo investigate the role of the low-density lipoprotein receptor-related protein ...
The formation and maintenance of the gross structure and microarchitecture of the human skeleton req...
Although Lrp5 is known to be an important contributor to the mechanisms regulating bone mass, its pr...
Objective. The wingless-type MMTV integration site family (WNT) signalling pathway plays an importan...
The low-density lipoprotein receptor-related protein (Lrp)-5 regulates osteoblast proliferation and ...
PURPOSE OF REVIEW: This review summarizes recent findings concerning the genomic variations of the l...
Skeletal health relies on architectural integrity and sufficient bone mass, which are maintained thr...
BACKGROUND: Primary osteoporosis is a rare childhood-onset skeletal condition whose pathogenesis has...
The human skeleton is affected by mutations in Low-density lipoprotein Receptor-related Protein 5 (L...
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, en...
Genetic studies in humans have shown loss-of-function mutations in the LRP5 gene to be responsible f...
In humans, low peak bone mass is a significant risk factor for osteoporosis. We report that LRP5, en...
AbstractIn humans, low peak bone mass is a significant risk factor for osteoporosis. We report that ...
The low density lipoprotein receptor-related protein-5 (LRP5) is a Wnt co-receptor that has been sho...
The low density lipoprotein receptor-related protein-5 (LRP5), a co-receptor in the Wnt signaling pa...
AbstractIntroductionTo investigate the role of the low-density lipoprotein receptor-related protein ...
The formation and maintenance of the gross structure and microarchitecture of the human skeleton req...
Although Lrp5 is known to be an important contributor to the mechanisms regulating bone mass, its pr...
Objective. The wingless-type MMTV integration site family (WNT) signalling pathway plays an importan...
The low-density lipoprotein receptor-related protein (Lrp)-5 regulates osteoblast proliferation and ...
PURPOSE OF REVIEW: This review summarizes recent findings concerning the genomic variations of the l...
Skeletal health relies on architectural integrity and sufficient bone mass, which are maintained thr...
BACKGROUND: Primary osteoporosis is a rare childhood-onset skeletal condition whose pathogenesis has...