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- W2332381854 endingPage "281" @default.
- W2332381854 startingPage "262" @default.
- W2332381854 abstract "Genomic technologies have evolved rapidly contributing to the understanding of diseases. Genome-wide association studies (GWAS) and whole-exome sequencing have aided the identification of the genetic determinants of monogenic and complex conditions including osteoporosis and bone mass disorders. Overlap exists between the genes implicated in monogenic and complex forms of bone mass disorders, largely explained by the clustering of genes encoding factors in signaling pathways crucial for mesenchymal cell differentiation, skeletal development, and bone remodeling and metabolism. Numerous of the remaining discovered genes merit functional follow-up studies to elucidate their role in bone biology. The insight provided by genetic studies is serving the identification of biomarkers predictive of disease, redefining disease, response to treatment, and discovery of novel drug targets for skeletal disorders." @default.
- W2332381854 created "2016-06-24" @default.
- W2332381854 creator A5064764888 @default.
- W2332381854 creator A5081737623 @default.
- W2332381854 date "2016-05-01" @default.
- W2332381854 modified "2023-10-16" @default.
- W2332381854 title "Osteoporosis and Bone Mass Disorders: From Gene Pathways to Treatments" @default.
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