Miyata I - Search Results

1

Overexpression of wild-type Akt1 promoted insulin-stimulated p70S6 kinase (p70S6K) activity and affected GSK3 beta regulation, but did not promote insulin-stimulated GLUT4 translocation or glucose transport in L6 myotubes.

Noda S, Kishi K, Yuasa T, Hayashi H, Ohnishi T, Miyata I, Nishitani H, Ebina Y. Noda S, et al. Among authors: miyata i. J Med Invest. 2000 Feb;47(1-2):47-55. J Med Invest. 2000. PMID: 10740979

2

Bradykinin directly triggers GLUT4 translocation via an insulin-independent pathway.

Kishi K, Muromoto N, Nakaya Y, Miyata I, Hagi A, Hayashi H, Ebina Y. Kishi K, et al. Among authors: miyata i. Diabetes. 1998 Apr;47(4):550-8. doi: 10.2337/diabetes.47.4.550. Diabetes. 1998. PMID: 9568686

3

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance.

Hosoe J, Kadowaki H, Miya F, Aizu K, Kawamura T, Miyata I, Satomura K, Ito T, Hara K, Tanaka M, Ishiura H, Tsuji S, Suzuki K, Takakura M, Boroevich KA, Tsunoda T, Yamauchi T, Shojima N, Kadowaki T. Hosoe J, et al. Among authors: miyata i. Diabetes. 2017 Oct;66(10):2713-2723. doi: 10.2337/db17-0301. Epub 2017 Aug 1. Diabetes. 2017. PMID: 28765322

4

Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.

Ono E, Ariga M, Oshima S, Hayakawa M, Imai M, Ochiai Y, Mochizuki H, Namba N, Ozono K, Miyata I. Ono E, et al. Among authors: miyata i. Clin Pediatr Endocrinol. 2016 Apr;25(2):23-35. doi: 10.1297/cpe.25.23. Epub 2016 Apr 28. Clin Pediatr Endocrinol. 2016. PMID: 27212794 Free PMC article.

5

Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.

Miyata I, Vallette-Kasic S, Saveanu A, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Reynaud R, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T. Miyata I, et al. J Clin Endocrinol Metab. 2006 Dec;91(12):4981-7. doi: 10.1210/jc.2005-2289. Epub 2006 Sep 12. J Clin Endocrinol Metab. 2006. PMID: 16968807

6

Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF).

Miyata I, Eto Y, Kamijo T, Ogawa M, Futrakul A, Phillips JA 3rd. Miyata I, et al. Endocr J. 1999 Mar;46 Suppl:S71-4. doi: 10.1507/endocrj.46.suppl_s71. Endocr J. 1999. PMID: 12054125 Free article. No abstract available.

7

A novel mutation of the arginine vasopressin receptor 2 gene in a patient with congenital nephrogenic diabetes insipidus.

Tajima A, Miyata I, Katayama A, Toyoda S, Eto Y. Tajima A, et al. Among authors: miyata i. Clin Pediatr Endocrinol. 2005;14(1):27-33. doi: 10.1297/cpe.14.27. Epub 2005 Feb 14. Clin Pediatr Endocrinol. 2005. PMID: 24790307 Free PMC article.

8

Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient.

Katagiri S, Hosono K, Hayashi T, Murai N, Wake E, Miyata I, Mizobuchi K, Kurata K, Matsuura T, Nakano T, Hotta Y. Katagiri S, et al. Among authors: miyata i. Doc Ophthalmol. 2020 Aug;141(1):77-88. doi: 10.1007/s10633-020-09752-5. Epub 2020 Jan 29. Doc Ophthalmol. 2020. PMID: 31997113

9

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

Sato N, Hasegawa T, Hasegawa Y, Arisaka O, Ozono K, Amemiya S, Kikuchi T, Tanaka H, Harada S, Miyata I, Tanaka T. Sato N, et al. Among authors: miyata i. Clin Pediatr Endocrinol. 2015 Apr;24(2):37-49. doi: 10.1297/cpe.24.37. Epub 2015 May 15. Clin Pediatr Endocrinol. 2015. PMID: 26019400 Free PMC article.

10

Constitutionally tall stature with morphological abnormality of the pituitary gland.

Miyata I, Yoshikawa H, Eto Y. Miyata I, et al. Endocr J. 2004 Apr;51(2):189-95. doi: 10.1507/endocrj.51.189. Endocr J. 2004. PMID: 15118269 Free article.

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