Michigami T - Search Results

1

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

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

[A case report of glomerulocystic kidney disease with hypothyroidism in a new born infant].

Satomura K, Michigami T, Yamamoto K, Hosokawa S. Satomura K, et al. Among authors: michigami t. Nihon Jinzo Gakkai Shi. 1998 Nov;40(8):602-6. Nihon Jinzo Gakkai Shi. 1998. PMID: 9893460 Japanese.

7

Analysis of the molecular mechanism for the antagonistic action of a novel 1alpha,25-dihydroxyvitamin D(3) analogue toward vitamin D receptor function.

Ozono K, Saito M, Miura D, Michigami T, Nakajima S, Ishizuka S. Ozono K, et al. Among authors: michigami t. J Biol Chem. 1999 Nov 5;274(45):32376-81. doi: 10.1074/jbc.274.45.32376. J Biol Chem. 1999. PMID: 10542279 Free article.

8

Identification of amino acid sequence in the hinge region of human vitamin D receptor that transfers a cytosolic protein to the nucleus.

Michigami T, Suga A, Yamazaki M, Shimizu C, Cai G, Okada S, Ozono K. Michigami T, et al. J Biol Chem. 1999 Nov 19;274(47):33531-8. doi: 10.1074/jbc.274.47.33531. J Biol Chem. 1999. PMID: 10559238 Free article.

9

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

10

Genomic organization of the human chondromodulin-1 gene containing a promoter region that confers the expression of reporter gene in chondrogenic ATDC5 cells.

Yanagihara I, Yamagata M, Sakai N, Shukunami C, Kurahashi H, Yamazaki M, Michigami T, Hiraki Y, Ozono K. Yanagihara I, et al. Among authors: michigami t. J Bone Miner Res. 2000 Mar;15(3):421-9. doi: 10.1359/jbmr.2000.15.3.421. J Bone Miner Res. 2000. PMID: 10750556 Free article.

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