Iwakura T - Search Results

1

Evaluation of a 1 step TRAb assay for the detection of high-affinity components to hTSHR: evidences indicating superiority of the assay in the lower TRAb range.

Ishihara T, Saiki Y, Ikekubo K, Hino M, Ikeda K, Son C, Iwakura T, Kobayashi H, Mori T. Ishihara T, et al. Among authors: iwakura t. Endocr J. 2006 Feb;53(1):147-55. doi: 10.1507/endocrj.53.147. Endocr J. 2006. PMID: 16543685 Free article.

2

A Novel homozygous missense mutation of melanocortin-4 receptor (MC4R) in a Japanese woman with severe obesity.

Kobayashi H, Ogawa Y, Shintani M, Ebihara K, Shimodahira M, Iwakura T, Hino M, Ishihara T, Ikekubo K, Kurahachi H, Nakao K. Kobayashi H, et al. Among authors: iwakura t. Diabetes. 2002 Jan;51(1):243-6. doi: 10.2337/diabetes.51.1.243. Diabetes. 2002. PMID: 11756348

3

Missense mutation of TRPS1 in a family of tricho-rhino-phalangeal syndrome type III.

Kobayashi H, Hino M, Shimodahira M, Iwakura T, Ishihara T, Ikekubo K, Ogawa Y, Nakao K, Kurahachi H. Kobayashi H, et al. Among authors: iwakura t. Am J Med Genet. 2002 Jan 1;107(1):26-9. doi: 10.1002/ajmg.10081. Am J Med Genet. 2002. PMID: 11807863

4

A case of TSH receptor antibody-positive hyperthyroidism with functioning metastases of thyroid carcinoma.

Ishihara T, Ikekubo K, Shimodahira M, Iwakura T, Kobayashi M, Hino M, Oobayashi M, Kohno K, Kimura K, Kawamura S, Kurahachi H. Ishihara T, et al. Among authors: iwakura t. Endocr J. 2002 Apr;49(2):241-5. doi: 10.1507/endocrj.49.241. Endocr J. 2002. PMID: 12081245 Free article.

5

GC79/TRPS1 and tumorigenesis in humans.

Kobayashi H, Hino M, Inoue T, Nii E, Ikeda K, Son C, Iwakura T, Ishihara T, Ogawa Y. Kobayashi H, et al. Among authors: iwakura t. Am J Med Genet A. 2005 Apr 30;134(3):341-3. doi: 10.1002/ajmg.a.30596. Am J Med Genet A. 2005. PMID: 15690404 No abstract available.

6

Immeasurably low and non-TRH-stimulatable TSH associated with normal I-123 uptake in two goitrous euthyroid patients: possible existence of other thyroid-hormone regulated thyroid stimulators other than TSH.

Ikekubo K, Hino M, Saiki Y, Son C, Iwakura T, Kobayashi H, Ishihara T. Ikekubo K, et al. Among authors: iwakura t. Endocr J. 2005 Feb;52(1):61-8. doi: 10.1507/endocrj.52.61. Endocr J. 2005. PMID: 15758559 Free article.

7

[No title available]

Kobayashi H, Shimodahira M, Iwakura T, Ishihara T, Kurahachi H, Hino M, Ikekubo K, Ogawa Y, Nakao K. Kobayashi H, et al. Among authors: iwakura t. Clin Calcium. 2002 Jan;12(1):124-7. Clin Calcium. 2002. PMID: 15775290 Japanese. No abstract available.

8

A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus.

Kobayashi H, Fujisawa I, Ikeda K, Son C, Iwakura T, Yoshimoto A, Kasahara M, Ishihara T, Ogawa Y. Kobayashi H, et al. Among authors: iwakura t. J Endocrinol Invest. 2006 Mar;29(3):252-6. doi: 10.1007/BF03345549. J Endocrinol Invest. 2006. PMID: 16682840

9

A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome.

Kobayashi H, Kasahara M, Hino M, Yoshimura H, Takahara S, Ikeda K, Son C, Iwakura T, Yoshimoto A, Ishihara T, Ogawa Y. Kobayashi H, et al. Among authors: iwakura t. J Endocrinol Invest. 2006 Oct;29(9):851-3. doi: 10.1007/BF03347383. J Endocrinol Invest. 2006. PMID: 17114920 No abstract available.

10

A novel heterozygous splice-site mutation of LEM domain-containing 3 in a Japanese kindred with Buschke-Ollendorff syndrome.

Kobayashi H, Kasahara M, Hino M, Takahara S, Ikeda K, Son C, Iwakura T, Matsuoka N, Yoshimoto A, Ohgo N, Kasai R, Ishihara T, Ogawa Y. Kobayashi H, et al. Among authors: iwakura t. J Endocrinol Invest. 2007 Mar;30(3):263-5. doi: 10.1007/BF03347437. J Endocrinol Invest. 2007. PMID: 17505164 No abstract available.

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