Fujioka M - Search Results

1

Rat gro/melanoma growth-stimulating activity. Assessment of the structure responsible for chemotactic activity by use of its fragments prepared by proteolysis and chemical synthesis.

Watanabe K, Fujioka M, Yokokawa H, Konishi K, Tsurufuji S, Nakagawa H. Watanabe K, et al. Among authors: fujioka m. Cytokine. 1992 Jan;4(1):12-7. doi: 10.1016/1043-4666(92)90030-u. Cytokine. 1992. PMID: 1617155

2

The neutrophil chemoattractant produced by the rat kidney epithelioid cell line NRK-52E is a protein related to the KC/gro protein.

Watanabe K, Konishi K, Fujioka M, Kinoshita S, Nakagawa H. Watanabe K, et al. Among authors: fujioka m. J Biol Chem. 1989 Nov 25;264(33):19559-63. J Biol Chem. 1989. PMID: 2684956 Free article.

3

Identification of cytokine-induced neutrophil chemoattractants (CINC), rat GRO/CINC-2 alpha and CINC-2 beta, produced by granulation tissue in culture: purification, complete amino acid sequences and characterization.

Nakagawa H, Komorita N, Shibata F, Ikesue A, Konishi K, Fujioka M, Kato H. Nakagawa H, et al. Among authors: fujioka m. Biochem J. 1994 Jul 15;301 ( Pt 2)(Pt 2):545-50. doi: 10.1042/bj3010545. Biochem J. 1994. PMID: 8043001 Free PMC article.

4

Recombinant expression of rat and human Gro proteins in Escherichia coli.

Konishi K, Takata Y, Watanabe K, Date T, Yamamoto M, Murase A, Yoshida H, Suzuki T, Tsurufuji S, Fujioka M. Konishi K, et al. Among authors: fujioka m. Cytokine. 1993 Sep;5(5):506-11. doi: 10.1016/1043-4666(93)90042-4. Cytokine. 1993. PMID: 8142607

5

Structure of the gene encoding rat neutrophil chemo-attractant Gro.

Konishi K, Takata Y, Yamamoto M, Yomogida K, Watanabe K, Tsurufuji S, Fujioka M. Konishi K, et al. Among authors: fujioka m. Gene. 1993 Apr 30;126(2):285-6. doi: 10.1016/0378-1119(93)90382-d. Gene. 1993. PMID: 8482545

6

The peptide sequences near the bound pyridoxal phosphate are conserved in serine dehydratase from rat liver, and threonine dehydratases from yeast and Escherichia coli.

Ogawa H, Konishi K, Fujioka M. Ogawa H, et al. Among authors: fujioka m. Biochim Biophys Acta. 1989 Jun 13;996(1-2):139-41. doi: 10.1016/0167-4838(89)90106-4. Biochim Biophys Acta. 1989. PMID: 2660911

7

Recombinant rat liver guanidinoacetate methyltransferase: reactivity and function of sulfhydryl groups.

Fujioka M, Konishi K, Takata Y. Fujioka M, et al. Biochemistry. 1988 Oct 4;27(20):7658-64. doi: 10.1021/bi00420a013. Biochemistry. 1988. PMID: 3207695

8

Rat liver glycine methyltransferase. Cooperative binding of S-adenosylmethionine and loss of cooperativity by removal of a short NH2-terminal segment.

Konishi K, Fujioka M. Konishi K, et al. Among authors: fujioka m. J Biol Chem. 1988 Sep 15;263(26):13381-5. J Biol Chem. 1988. PMID: 3417662 Free article.

Rat liver glycine methyltransferase, a homotetramer, exhibits sigmoidal rate behavior with respect to S-adenosylmethionine (Ogawa, H., and Fujioka, M. (1982) J. Biol. Chem. 257, 3447-3452). The binding experiment shows that the sigmoidicity observed in initial veloc …

Rat liver glycine methyltransferase, a homotetramer, exhibits sigmoidal rate behavior with respect to S-adenosylmethionine (Ogawa, H., and …

9

Chemical modification of a functional arginine residue of rat liver glycine methyltransferase.

Konishi K, Fujioka M. Konishi K, et al. Among authors: fujioka m. Biochemistry. 1987 Dec 15;26(25):8496-502. doi: 10.1021/bi00399a069. Biochemistry. 1987. PMID: 3442671

10

Function and reactivity of sulfhydryl groups of rat liver glycine methyltransferase.

Fujioka M, Takata Y, Konishi K, Ogawa H. Fujioka M, et al. Biochemistry. 1987 Sep 8;26(18):5696-702. doi: 10.1021/bi00392a018. Biochemistry. 1987. PMID: 3676278

Besides this residue, Cys-185, Cys-246, and Cys-262 are modified upon prolonged incubation with iodoacetate. 5'-[p-(Fluorosulfonyl)benzoyl]adenosine (FSBA) inactivates glycine methyltransferase by forming 1 disulfide/subunit [Fujioka, M., & Ishiguro, Y. (1986) J …

Besides this residue, Cys-185, Cys-246, and Cys-262 are modified upon prolonged incubation with iodoacetate. 5'-[p-(Fluorosulfonyl)benzoyl]a …

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