Miyagi M - Search Results

1

A novel derivatization method with 5-bromonicotinic acid N-hydroxysuccinimide for determination of the amino acid sequences of peptides.

Miyagi M, Nakao M, Nakazawa T, Kato I, Tsunasawa S. Miyagi M, et al. Rapid Commun Mass Spectrom. 1998;12(10):603-8. doi: 10.1002/(SICI)1097-0231(19980529)12:10<603::AID-RCM204>3.0.CO;2-0. Rapid Commun Mass Spectrom. 1998. PMID: 9621443

2

Antibodies against 70-kD heat shock cognate protein inhibit mediated nuclear import of karyophilic proteins.

Imamoto N, Matsuoka Y, Kurihara T, Kohno K, Miyagi M, Sakiyama F, Okada Y, Tsunasawa S, Yoneda Y. Imamoto N, et al. Among authors: miyagi m. J Cell Biol. 1992 Dec;119(5):1047-61. doi: 10.1083/jcb.119.5.1047. J Cell Biol. 1992. PMID: 1332978 Free PMC article.

3

NH2-terminal acetylation of ribosomal proteins of Saccharomyces cerevisiae.

Takakura H, Tsunasawa S, Miyagi M, Warner JR. Takakura H, et al. Among authors: miyagi m. J Biol Chem. 1992 Mar 15;267(8):5442-5. J Biol Chem. 1992. PMID: 1544921 Free article.

4

Overproduction of Thermus aquaticus DNA polymerase and its structural analysis by ion-spray mass spectrometry.

Ishino Y, Ueno T, Miyagi M, Uemori T, Imamura M, Tsunasawa S, Kato I. Ishino Y, et al. Among authors: miyagi m. J Biochem. 1994 Nov;116(5):1019-24. doi: 10.1093/oxfordjournals.jbchem.a124622. J Biochem. 1994. PMID: 7896728 Free article.

5

A peptide that stimulates phosphorylation of the plant insulin-binding protein. Isolation, primary structure and cDNA cloning.

Watanabe Y, Barbashov SF, Komatsu S, Hemmings AM, Miyagi M, Tsunasawa S, Hirano H. Watanabe Y, et al. Among authors: miyagi m. Eur J Biochem. 1994 Aug 15;224(1):167-72. doi: 10.1111/j.1432-1033.1994.tb20008.x. Eur J Biochem. 1994. PMID: 8076638 Free article.

6

Lymphocyte isoforms of mouse p50 LSP1, which are phosphorylated in mitogen-activated T cells, are formed through alternative splicing and phosphorylation.

Matsumoto N, Kita K, Kojima S, Yamamoto K, Irimura T, Miyagi M, Tsunasawa S, Toyoshima S. Matsumoto N, et al. Among authors: miyagi m. J Biochem. 1995 Jul;118(1):237-43. doi: 10.1093/oxfordjournals.jbchem.a124885. J Biochem. 1995. PMID: 8537319 Free article.

7

Complete covalent structure of porcine liver acylamino acid-releasing enzyme and identification of its active site serine residue.

Miyagi M, Sakiyama F, Kato I, Tsunasawa S. Miyagi M, et al. J Biochem. 1995 Oct;118(4):771-9. doi: 10.1093/oxfordjournals.jbchem.a124979. J Biochem. 1995. PMID: 8576092 Free article.

8

Amino acid sequence and carbohydrate structure of a recombinant human tissue factor pathway inhibitor expressed in Chinese hamster ovary cells: one N-and two O-linked carbohydrate chains are located between Kunitz domains 2 and 3 and one N-linked carbohydrate chain is in Kunitz domain 2.

Nakahara Y, Miyata T, Hamuro T, Funatsu A, Miyagi M, Tsunasawa S, Kato H. Nakahara Y, et al. Among authors: miyagi m. Biochemistry. 1996 May 21;35(20):6450-9. doi: 10.1021/bi9524880. Biochemistry. 1996. PMID: 8639592

9

A cysteine protease inhibitor stored in the large granules of horseshoe crab hemocytes: purification, characterization, cDNA cloning and tissue localization.

Agarwala KL, Kawabata S, Hirata M, Miyagi M, Tsunasawa S, Iwanaga S. Agarwala KL, et al. Among authors: miyagi m. J Biochem. 1996 Jan;119(1):85-94. doi: 10.1093/oxfordjournals.jbchem.a021220. J Biochem. 1996. PMID: 8907180 Free article.

10

Paracatalytic inactivation of L-2-haloacid dehalogenase from Pseudomonas sp. YL by hydroxylamine. Evidence for the formation of an ester intermediate.

Liu JQ, Kurihara T, Miyagi M, Tsunasawa S, Nishihara M, Esaki N, Soda K. Liu JQ, et al. Among authors: miyagi m. J Biol Chem. 1997 Feb 7;272(6):3363-8. doi: 10.1074/jbc.272.6.3363. J Biol Chem. 1997. PMID: 9013577 Free article.

YL was proposed to act as a nucleophile to attack the alpha-carbon of L-2-haloalkanoic acids to form an ester intermediate, which is hydrolyzed by nucleophilic attack of a water molecule on the carbonyl carbon (Liu, J.-Q, Kurihara, T., Miyagi, M., Esaki, N., and Sod …

YL was proposed to act as a nucleophile to attack the alpha-carbon of L-2-haloalkanoic acids to form an ester intermediate, which is hydroly …

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