# Editorial: Genetic and molecular determinants in bone health and diseases

**Authors:** Michela Rossi, Jonathan W. Lowery, Andrea Del Fattore

PMC · DOI: 10.3389/fendo.2024.1347765 · 2024-01-17

## Full-text entities

- **Genes:** ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 249] {aka AP-TNAP, APTNAP, HOPS, HPPA, HPPC, HPPI}, NRP2 (neuropilin 2) [NCBI Gene 8828] {aka NP2, NPN2, PRO2714, VEGF165R2}, COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277] {aka CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, COL1A2 (collagen type I alpha 2 chain) [NCBI Gene 1278] {aka EDSARTH2, EDSCV, OI4}, ATHS (atherosclerosis susceptibility (lipoprotein associated)) [NCBI Gene 470] {aka ALP}, MBTPS2 (membrane bound transcription factor peptidase, site 2) [NCBI Gene 51360] {aka BRESEK, IFAP, KFSD, KFSDX, OI19, OLMSX}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}
- **Diseases:** OI (MESH:D010013), diseases (MESH:D004194), hip and knee osteoarthritis (MESH:D020370), osteoporosis (MESH:D010024), micromelia (MESH:C565382), non-bacterial osteomyelitis (MESH:D010019), fragility (MESH:D005600), bone dysplasia (MESH:D001848), inflammatory (MESH:D007249), malnutrition (MESH:D044342), resorption (MESH:D014091), defective ossification of (MESH:C562735), deficiency of myeloperoxidase (MESH:C562864), AD (MESH:D000544), hypophosphatasia (MESH:D007014), angiomatous (MESH:D008579), Vanishing Bone Disease (MESH:D001847), genetic disease (MESH:D030342), rheumatoid arthritis (MESH:D001172), osteolysis (MESH:D010014), Gorham-Stout disease (MESH:D010015)
- **Chemicals:** bisphosphonates (MESH:D004164), fatty acid (MESH:D005227), adalimumab (MESH:D000068879), IL1-receptor antagonists (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Cercopithecidae (monkey, family) [taxon 9527]

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Source: https://tomesphere.com/paper/PMC10832011