Ozono K - Search Results

1

Parental somatogonadal COL2A1 mosaicism contributes to intrafamilial recurrence in a family with type 2 collagenopathy.

Yamamoto K, Kubota T, Takeyari S, Kitaoka T, Miyata K, Nakano Y, Nakayama H, Ohata Y, Yanagi K, Kaname T, Okada Y, Ozono K. Yamamoto K, et al. Among authors: ozono k. Am J Med Genet A. 2020 Mar;182(3):454-460. doi: 10.1002/ajmg.a.61422. Epub 2019 Dec 19. Am J Med Genet A. 2020. PMID: 31854518

2

Bone marrow-derived osteoclast-like cells from a patient with craniometaphyseal dysplasia lack expression of osteoclast-reactive vacuolar proton pump.

Yamamoto T, Kurihara N, Yamaoka K, Ozono K, Okada M, Yamamoto K, Matsumoto S, Michigami T, Ono J, Okada S. Yamamoto T, et al. Among authors: ozono k. J Clin Invest. 1993 Jan;91(1):362-7. doi: 10.1172/JCI116194. J Clin Invest. 1993. PMID: 7678608 Free PMC article.

3

Mutational analysis of the DTDST gene in a fetus with achondrogenesis type 1B.

Cai G, Nakayama M, Hiraki Y, Ozono K. Cai G, et al. Among authors: ozono k. Am J Med Genet. 1998 Jun 16;78(1):58-60. Am J Med Genet. 1998. PMID: 9637425

4

Hyperintensity of posterior pituitary on MR T1WI in a boy with central diabetes insipidus caused by missense mutation of neurophysin II gene.

Kubota T, Yamamoto T, Ozono K, Shimotsuji T. Kubota T, et al. Among authors: ozono k. Endocr J. 2001 Aug;48(4):459-63. doi: 10.1507/endocrj.48.459. Endocr J. 2001. PMID: 11603568 Free article.

5

[Regulation of bone mineralization by enzymes].

Kubota T, Ozono K. Kubota T, et al. Among authors: ozono k. Clin Calcium. 2004 Jun;14(6):23-7. Clin Calcium. 2004. PMID: 15577050 Review. Japanese.

6

[Osteoporosis associated with gene mutation].

Ozono K, Kubota T. Ozono K, et al. Clin Calcium. 2003 Dec;13(12):1523-9. Clin Calcium. 2003. PMID: 15775238 Japanese.

7

[Albright hereditary osteodystrophy].

Kitaoka T, Ozono K. Kitaoka T, et al. Among authors: ozono k. Nihon Rinsho. 2006 Jun 28;Suppl 2:61-5. Nihon Rinsho. 2006. PMID: 16817351 Review. Japanese. No abstract available.

8

Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter.

Namba N, Etani Y, Kitaoka T, Nakamoto Y, Nakacho M, Bessho K, Miyoshi Y, Mushiake S, Mohri I, Arai H, Taniike M, Ozono K. Namba N, et al. Among authors: ozono k. Eur J Pediatr. 2008 Jul;167(7):785-91. doi: 10.1007/s00431-007-0589-6. Epub 2007 Sep 25. Eur J Pediatr. 2008. PMID: 17899191

9

PTH/cAMP/PKA signaling facilitates canonical Wnt signaling via inactivation of glycogen synthase kinase-3beta in osteoblastic Saos-2 cells.

Suzuki A, Ozono K, Kubota T, Kondou H, Tachikawa K, Michigami T. Suzuki A, et al. Among authors: ozono k. J Cell Biochem. 2008 May 1;104(1):304-17. doi: 10.1002/jcb.21626. J Cell Biochem. 2008. PMID: 17990294

10

Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with Mesd.

Kubota T, Michigami T, Sakaguchi N, Kokubu C, Suzuki A, Namba N, Sakai N, Nakajima S, Imai K, Ozono K. Kubota T, et al. Among authors: ozono k. J Bone Miner Res. 2008 Oct;23(10):1661-71. doi: 10.1359/jbmr.080512. J Bone Miner Res. 2008. PMID: 18505367 Free article.

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