Morishita M - Search Results

1

Dihydrofolate reductase gene intronic 19-bp deletion polymorphisms in a Japanese population.

Hayashi H, Horino M, Morishita M, Tazoe Y, Tsuboi S, Matsuyama T, Kosuge K, Yamada H, Tsuji D, Inoue K, Itoh K. Hayashi H, et al. Among authors: morishita m. Drug Metab Pharmacokinet. 2010;25(5):516-8. doi: 10.2133/dmpk.dmpk-10-sc-036. Epub 2010 Sep 7. Drug Metab Pharmacokinet. 2010. PMID: 20834190 Free article.

2

A single nucleotide polymorphism of reduced folate carrier 1 predicts methotrexate efficacy in Japanese patients with rheumatoid arthritis.

Hayashi H, Tazoe Y, Tsuboi S, Horino M, Morishita M, Arai T, Ohshima M, Matsuyama T, Kosuge K, Yamada H, Tsuji D, Inoue K, Itoh K. Hayashi H, et al. Among authors: morishita m. Drug Metab Pharmacokinet. 2013;28(2):164-8. doi: 10.2133/dmpk.dmpk-12-nt-038. Epub 2012 Sep 11. Drug Metab Pharmacokinet. 2013. PMID: 22971639 Free article. Clinical Trial.

3

The effects of GH-releasing hormone/somatostatin on the 5'-promoter activity of the GH gene in vitro.

Morishita M, Iwasaki Y, Onishi A, Asai M, Mutsuga N, Yoshida M, Oiso Y, Inoue K, Murohara T. Morishita M, et al. J Mol Endocrinol. 2003 Dec;31(3):441-8. doi: 10.1677/jme.0.0310441. J Mol Endocrinol. 2003. PMID: 14664705

4

Three Japanese families with Hb H disease: gene analyses and their characterizations.

Hattori Y, Morishita M, Yamashiro Y, Yamamoto K, Yamamoto K, Matsuno Y, Ohba Y, Miyaji T. Hattori Y, et al. Among authors: morishita m. Hemoglobin. 1990;14(5):559-67. doi: 10.3109/03630269009005809. Hemoglobin. 1990. PMID: 2079436 No abstract available.

5

Studies on the intestinal absorption characteristics of sulfasalazine, a breast cancer resistance protein (BCRP) substrate.

Tomaru A, Morimoto N, Morishita M, Takayama K, Fujita T, Maeda K, Kusuhara H, Sugiyama Y. Tomaru A, et al. Among authors: morishita m. Drug Metab Pharmacokinet. 2013;28(1):71-4. doi: 10.2133/dmpk.dmpk-12-nt-024. Epub 2012 Jul 3. Drug Metab Pharmacokinet. 2013. PMID: 22785334 Free article.

6

[A Japanese family with hereditary HbH disease--a case report and its gene analysis].

Hattori Y, Yamashiro Y, Yamamoto K, Morishita M, Miyaji T, Yamamoto K, Matsuno Y, Fujii H, Miwa S, Ichimaru M. Hattori Y, et al. Among authors: morishita m. Rinsho Ketsueki. 1990 Feb;31(2):183-8. Rinsho Ketsueki. 1990. PMID: 2329681 Japanese.

7

Three beta-thalassemia mutations in the Japanese: IVS-II-1 (G----A), IVS-II-848 (C----G), and codon 90 (GAG----TAG).

Hattori Y, Yamamoto K, Yamashiro Y, Ohba Y, Miyamura S, Yamamoto K, Matsuno Y, Morishita M, Miyaji T, Era T. Hattori Y, et al. Among authors: morishita m. Hemoglobin. 1992;16(1-2):93-7. doi: 10.3109/03630269209005682. Hemoglobin. 1992. PMID: 1634368 No abstract available.

8

Homeobox protein Gsh-1-dependent regulation of the rat GHRH gene promoter.

Mutsuga N, Iwasaki Y, Morishita M, Nomura A, Yamamori E, Yoshida M, Asai M, Ozaki N, Kambe F, Seo H, Oiso Y, Saito H. Mutsuga N, et al. Among authors: morishita m. Mol Endocrinol. 2001 Dec;15(12):2149-56. doi: 10.1210/mend.15.12.0747. Mol Endocrinol. 2001. PMID: 11731616

9

Antidiabetic sulfonylurea enhances secretagogue-induced adrenocorticotropin secretion and proopiomelanocortin gene expression in vitro.

Morishita M, Iwasaki Y, Yamamori E, Nomura A, Mutsuga N, Yoshida M, Asai M, Oiso Y, Saito H. Morishita M, et al. Endocrinology. 2000 Sep;141(9):3313-8. doi: 10.1210/endo.141.9.7655. Endocrinology. 2000. PMID: 10965903

10

Involvement of upstream open reading frames in regulation of rat V(1b) vasopressin receptor expression.

Nomura A, Iwasaki Y, Saito M, Aoki Y, Yamamori E, Ozaki N, Tachikawa K, Mutsuga N, Morishita M, Yoshida M, Asai M, Oiso Y, Saito H. Nomura A, et al. Among authors: morishita m. Am J Physiol Endocrinol Metab. 2001 May;280(5):E780-7. doi: 10.1152/ajpendo.2001.280.5.E780. Am J Physiol Endocrinol Metab. 2001. PMID: 11287361 Free article.

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