Fragilitas ossium (fro): an autosomal recessive mutation in the mouse
- PMID: 7122619
Fragilitas ossium (fro): an autosomal recessive mutation in the mouse
Similar articles
-
Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta.Am J Med Genet. 1993 Jan 15;45(2):276-83. doi: 10.1002/ajmg.1320450227. Am J Med Genet. 1993. PMID: 8456819
-
Fragilitas ossium: a new autosomal recessive mutation in the mouse.J Hered. 1981 Nov-Dec;72(6):440-1. doi: 10.1093/oxfordjournals.jhered.a109554. J Hered. 1981. PMID: 6801109
-
Is the lingual forming part of the incisor a structural entity? Evidences from the fragilitas ossium (fro/fro) mouse mutation and the TGFbeta1 overexpressing transgenic strain.Arch Oral Biol. 2005 Feb;50(2):279-86. doi: 10.1016/j.archoralbio.2004.09.009. Epub 2004 Nov 11. Arch Oral Biol. 2005. PMID: 15721162
-
[Attempts to use gene therapy for reducing connective tissue disorders--osteogenesis imperfecta].Postepy Biochem. 2003;49(1):18-25. Postepy Biochem. 2003. PMID: 14518394 Review. Polish. No abstract available.
-
Osteogenesis imperfecta: prospects for molecular therapeutics.Mol Genet Metab. 2000 Sep-Oct;71(1-2):225-32. doi: 10.1006/mgme.2000.3039. Mol Genet Metab. 2000. PMID: 11001814 Review.
Cited by
-
Deficiency of sphingomyelin synthase 1 but not sphingomyelin synthase 2 reduces bone formation due to impaired osteoblast differentiation.Mol Med. 2019 Dec 17;25(1):56. doi: 10.1186/s10020-019-0123-0. Mol Med. 2019. PMID: 31847800 Free PMC article.
MeSH terms
LinkOut - more resources
Medical