Kubota T - Search Results

1

Skeletal defects in ringelschwanz mutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesis.

Kokubu C, Heinzmann U, Kokubu T, Sakai N, Kubota T, Kawai M, Wahl MB, Galceran J, Grosschedl R, Ozono K, Imai K. Kokubu C, et al. Among authors: kubota t. Development. 2004 Nov;131(21):5469-80. doi: 10.1242/dev.01405. Epub 2004 Oct 6. Development. 2004. PMID: 15469977

2

[Regulation of bone mineralization by enzymes].

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

3

[Osteoporosis associated with gene mutation].

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

4

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: kubota t. J Cell Biochem. 2008 May 1;104(1):304-17. doi: 10.1002/jcb.21626. J Cell Biochem. 2008. PMID: 17990294

5

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. J Bone Miner Res. 2008 Oct;23(10):1661-71. doi: 10.1359/jbmr.080512. J Bone Miner Res. 2008. PMID: 18505367 Free article.

6

Wnt signaling in bone metabolism.

Kubota T, Michigami T, Ozono K. Kubota T, et al. J Bone Miner Metab. 2009;27(3):265-71. doi: 10.1007/s00774-009-0064-8. Epub 2009 Mar 31. J Bone Miner Metab. 2009. PMID: 19333681 Review.

7

[Wnt signaling molecules related to osteoporosis].

Kubota T, Ozono K. Kubota T, et al. Clin Calcium. 2013 Jun;23(6):855-60. Clin Calcium. 2013. PMID: 23719498 Review. Japanese.

8

Wnt signaling in bone.

Kubota T, Michigami T, Ozono K. Kubota T, et al. Clin Pediatr Endocrinol. 2010 Jul;19(3):49-56. doi: 10.1297/cpe.19.49. Epub 2010 Aug 31. Clin Pediatr Endocrinol. 2010. PMID: 23926379 Free PMC article.

9

CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B.

Yamamoto K, Kawai M, Yamazaki M, Tachikawa K, Kubota T, Ozono K, Michigami T. Yamamoto K, et al. Among authors: kubota t. Hum Mol Genet. 2019 Apr 1;28(7):1183-1198. doi: 10.1093/hmg/ddy428. Hum Mol Genet. 2019. PMID: 30544148

10

Metreleptin treatment for congenital generalized lipodystrophy type 4 (CGL4): a case report.

Takeyari S, Takakuwa S, Miyata K, Yamamoto K, Nakayama H, Ohata Y, Fujiwara M, Kitaoka T, Kubota T, Namba N, Sakai N, Ozono K. Takeyari S, et al. Among authors: kubota t. Clin Pediatr Endocrinol. 2019;28(1):1-7. doi: 10.1297/cpe.28.1. Epub 2019 Jan 31. Clin Pediatr Endocrinol. 2019. PMID: 30745727 Free PMC article.

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