Michigami T - Search Results

1

Clinical Practice Guidelines for Hypophosphatasia.

Michigami T, Ohata Y, Fujiwara M, Mochizuki H, Adachi M, Kitaoka T, Kubota T, Sawai H, Namba N, Hasegawa K, Fujiwara I, Ozono K. Michigami T, et al. Clin Pediatr Endocrinol. 2020;29(1):9-24. doi: 10.1297/cpe.29.9. Epub 2020 Jan 9. Clin Pediatr Endocrinol. 2020. PMID: 32029969 Free PMC article.

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: michigami t. J Clin Invest. 1993 Jan;91(1):362-7. doi: 10.1172/JCI116194. J Clin Invest. 1993. PMID: 7678608 Free PMC article.

3

Increased IL-6-production by cells isolated from the fibrous bone dysplasia tissues in patients with McCune-Albright syndrome.

Yamamoto T, Ozono K, Kasayama S, Yoh K, Hiroshima K, Takagi M, Matsumoto S, Michigami T, Yamaoka K, Kishimoto T, Okada S. Yamamoto T, et al. Among authors: michigami t. J Clin Invest. 1996 Jul 1;98(1):30-5. doi: 10.1172/JCI118773. J Clin Invest. 1996. PMID: 8690800 Free PMC article.

4

Hypercalcemia associated with infantile fibrosarcoma producing parathyroid hormone-related protein.

Michigami T, Yamato H, Mushiake S, Nakayama M, Yoneda A, Satomura K, Imura K, Ozono K. Michigami T, et al. J Clin Endocrinol Metab. 1996 Mar;81(3):1090-5. doi: 10.1210/jcem.81.3.8772581. J Clin Endocrinol Metab. 1996. PMID: 8772581

5

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia.

Ozono K, Yamagata M, Michigami T, Nakajima S, Sakai N, Cai G, Satomura K, Yasui N, Okada S, Nakayama M. Ozono K, et al. Among authors: michigami t. J Clin Endocrinol Metab. 1996 Dec;81(12):4458-61. doi: 10.1210/jcem.81.12.8954059. J Clin Endocrinol Metab. 1996. PMID: 8954059

6

Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimeras.

Cai G, Michigami T, Yamamoto T, Yasui N, Satomura K, Yamagata M, Shima M, Nakajima S, Mushiake S, Okada S, Ozono K. Cai G, et al. Among authors: michigami t. J Clin Endocrinol Metab. 1998 Nov;83(11):3936-42. doi: 10.1210/jcem.83.11.5267. J Clin Endocrinol Metab. 1998. PMID: 9814472

7

Asp361Val Mutant of alkaline phosphatase found in patients with dominantly inherited hypophosphatasia inhibits the activity of the wild-type enzyme.

Müller HL, Yamazaki M, Michigami T, Kageyama T, Schönau E, Schneider P, Ozono K. Müller HL, et al. Among authors: michigami t. J Clin Endocrinol Metab. 2000 Feb;85(2):743-7. doi: 10.1210/jcem.85.2.6373. J Clin Endocrinol Metab. 2000. PMID: 10690885

8

Severe hypercalcaemia and respiratory insufficiency associated with infantile hypophosphatasia caused by two novel mutations of the tissue-nonspecific alkaline phosphatase gene.

Mochizuki H, Saito M, Michigami T, Ohashi H, Koda N, Yamaguchi S, Ozono K. Mochizuki H, et al. Among authors: michigami t. Eur J Pediatr. 2000 May;159(5):375-9. doi: 10.1007/s004310051290. Eur J Pediatr. 2000. PMID: 10834525

9

Receptor activator of nuclear factor kappaB ligand (RANKL) is a key molecule of osteoclast formation for bone metastasis in a newly developed model of human neuroblastoma.

Michigami T, Ihara-Watanabe M, Yamazaki M, Ozono K. Michigami T, et al. Cancer Res. 2001 Feb 15;61(4):1637-44. Cancer Res. 2001. PMID: 11245477

10

A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia.

Hirai H, Nakajima S, Miyauchi A, Nishimura K, Shimizu N, Shima M, Michigami T, Ozono K, Okada S. Hirai H, et al. Among authors: michigami t. J Hum Genet. 2001;46(1):41-4. doi: 10.1007/s100380170124. J Hum Genet. 2001. PMID: 11289719

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