Hishinuma A - Search Results

1

[Inherited defects of thyroid hormone biosynthesis].

Ieiri T, Hishinuma A, Shimoda S. Ieiri T, et al. Among authors: hishinuma a. Ryoikibetsu Shokogun Shirizu. 1993;(1):303-5. Ryoikibetsu Shokogun Shirizu. 1993. PMID: 7757591 Review. Japanese. No abstract available.

2

Effects of epidermal growth factor, phorbol ester, and retinoic acid on hormone synthesis and morphology in porcine thyroid follicles cultured in collagen gel.

Hishinuma A, Kasai K, Ichimura K, Emoto T, Shimoda S. Hishinuma A, et al. Thyroid. 1992 Winter;2(4):351-9. doi: 10.1089/thy.1992.2.351. Thyroid. 1992. PMID: 1493378

3

Effects of inorganic iodide, epidermal growth factor and phorbol ester on hormone synthesis by porcine thyroid follicles cultured in suspension.

Kasai K, Yamaguchi F, Hosoya T, Ichimura K, Banba N, Emoto T, Hiraiwa M, Hishinuma A, Hattori Y, Shimoda S. Kasai K, et al. Among authors: hishinuma a. Life Sci. 1992;51(14):1095-103. doi: 10.1016/0024-3205(92)90510-v. Life Sci. 1992. PMID: 1518372

4

[Congenital goiter].

Hishinuma A, Ieiri T, Shimoda S. Hishinuma A, et al. Ryoikibetsu Shokogun Shirizu. 1993;(1):300-2. Ryoikibetsu Shokogun Shirizu. 1993. PMID: 7757590 Review. Japanese. No abstract available.

5

Different growth control of the two human thyroid cell lines of adenomatous goiter and papillary carcinoma.

Hishinuma A, Yamanaka T, Kasai K, So S, Tseng CC, Bamba N, Ohtake H, Shimoda S. Hishinuma A, et al. Thyroid. 1995 Feb;5(1):41-6. doi: 10.1089/thy.1995.5.41. Thyroid. 1995. PMID: 7787432

6

[Thyroxine-binding proteins--familial euthyroid hyperthyroxinemia due to point mutations of transthyretin].

Hishinuma A, Mochizuki Y, Kasai K, Shimoda S. Hishinuma A, et al. Nihon Rinsho. 1994 Apr;52(4):886-9. Nihon Rinsho. 1994. PMID: 8196175 Review. Japanese.

7

Growth regulation of the human papillary thyroid cancer cell line by protein tyrosine kinase and cAMP-dependent protein kinase.

Hishinuma A, Yamanaka T, Kasai K, So S, Bamba N, Shimoda SI. Hishinuma A, et al. Endocr J. 1994 Aug;41(4):399-407. doi: 10.1507/endocrj.41.399. Endocr J. 1994. PMID: 8528355 Free article.

8

Analysis of the promoter of the thyrotropin receptor gene and the entire genomic sequence of thyroid transcription factor-1 in familial congenital hypothyroidism due to thyrotropin unresponsiveness.

Hishinuma A, Takamatsu J, Kanno Y, Yoshida S, Ieiri T. Hishinuma A, et al. Thyroid. 1998 Apr;8(4):305-9. doi: 10.1089/thy.1998.8.305. Thyroid. 1998. PMID: 9588495

9

Missense mutation (C1263R) in the thyroglobulin gene causes congenital goiter with mild hypothyroidism by impaired intracellular transport.

Hishinuma A, Kasai K, Masawa N, Kanno Y, Arimura M, Shimoda SI, Ieiri T. Hishinuma A, et al. Endocr J. 1998 Jun;45(3):315-27. doi: 10.1507/endocrj.45.315. Endocr J. 1998. PMID: 9790265 Free article.

10

[Recent advance in the thyroid testing with special reference to the gene analysis].

Ieiri T, Hishinuma A. Ieiri T, et al. Among authors: hishinuma a. Rinsho Byori. 1998 Nov;46(11):1071-81. Rinsho Byori. 1998. PMID: 9868291 Review. Japanese.

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