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Current OI mouse models with a glycine substitution in\n                    <jats:italic>Col1a1<\/jats:italic>\n                    exhibit excessive severity, thereby limiting long-term pathophysiological analysis and drug effect assessments. To address this limitation, we constructed a novel OI mouse model mimicking a patient with OI type III. This was achieved by introducing a G-to-A transversion at nucleotide position 2428 in the\n                    <jats:italic>Col1a1<\/jats:italic>\n                    gene via CRISPR-Cas9 technology in C57BL\/6\u00a0J mice. The resulting heterozygous variant mice (\n                    <jats:italic>Col1a1<\/jats:italic>\n                    <jats:sup>G643S\/+<\/jats:sup>\n                    ) displayed reduced body weight and pronounced skeletal abnormalities. Micro-CT analysis at 12\u00a0weeks revealed decreased vertebral bone parameters and altered cortical bone characteristics, indicative of bone fragility. Additionally, the abnormalities of the anisotropy, complexity, connectivity, and structure of trabecular bone were revealed. A three-point bending test confirmed the fragility, with reduced displacement and fracture energy in both sexes. Furthermore, we evaluated the effect of 4-phenylbutyric acid on the bone in\n                    <jats:italic>Col1a1<\/jats:italic>\n                    <jats:sup>G643S\/+<\/jats:sup>\n                    mice at 12\u00a0weeks, observing no significant effects, likely due to the absence of collagen retention in the ER in this model. Despite being a moderate OI model,\n                    <jats:italic>Col1a1<\/jats:italic>\n                    <jats:sup>G643S\/+<\/jats:sup>\n                    mice manifest a distinct and fragile bone phenotype, making them suitable for extended studies. This model offers a valuable platform for investigating long-term pathophysiological aspects of OI and assessing the efficacy of potential therapeutic interventions.\n                  <\/jats:p>","DOI":"10.1007\/s00223-024-01320-2","type":"journal-article","created":{"date-parts":[[2025,1,3]],"date-time":"2025-01-03T02:35:00Z","timestamp":1735871700000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Characterization of a Novel Col1a1G643S\/+ Osteogenesis Imperfecta Mouse Model with Insights into Skeletal Phenotype, Fragility, and Therapeutic Evaluations"],"prefix":"10.1007","volume":"116","author":[{"ORCID":"https:\/\/orcid.org\/0009-0001-0161-9695","authenticated-orcid":false,"given":"Hiroyuki","family":"Saitou","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6084-6620","authenticated-orcid":false,"given":"Yasuhisa","family":"Ohata","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3627-1932","authenticated-orcid":false,"given":"Shinji","family":"Takeyari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0000-4799-1049","authenticated-orcid":false,"given":"Chiaki","family":"Nishizawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-5142-6822","authenticated-orcid":false,"given":"Hirofumi","family":"Nakayama","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6799-9774","authenticated-orcid":false,"given":"Makoto","family":"Fujiwara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2907-9512","authenticated-orcid":false,"given":"Yasuji","family":"Kitabatake","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4483-4405","authenticated-orcid":false,"given":"Takuo","family":"Kubota","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6517-8825","authenticated-orcid":false,"given":"Keiichi","family":"Ozono","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2025,1,3]]},"reference":[{"key":"1320_CR1","doi-asserted-by":"publisher","first-page":"101","DOI":"10.1136\/jmg.16.2.101","volume":"16","author":"DO Sillence","year":"1979","unstructured":"Sillence DO, Senn A, Danks DM (1979) Genetic heterogeneity in osteogenesis imperfecta. 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