Imajoh-Ohmi S - Search Results

1

Two brothers with p47-phox-deficient chronic granulomatous disease associated with end-stage renal failure.

Yamazaki H, Nishi S, Chou T, Nakagawa Y, Shimada H, Nunoi H, Imajoh-Ohmi S, Yoshioka K, Arakawa M. Yamazaki H, et al. Nephrol Dial Transplant. 1995 Dec;10(12):2334-6. doi: 10.1093/ndt/10.12.2334. Nephrol Dial Transplant. 1995. PMID: 8808236 No abstract available.

2

Peptides corresponding to the region adjacent to His-94 in the small subunit of cytochrome b558 inhibit superoxide generation in a cell-free system from human neutrophils.

Park MY, Imajoh-Ohmi S, Nunoi H, Kanegasaki S. Park MY, et al. Biochem Biophys Res Commun. 1994 Oct 28;204(2):924-9. doi: 10.1006/bbrc.1994.2548. Biochem Biophys Res Commun. 1994. PMID: 7980562

3

Synthetic peptides corresponding to various hydrophilic regions of the large subunit of cytochrome b558 inhibit superoxide generation in a cell-free system from neutrophils.

Park MY, Imajoh-Ohmi S, Nunoi H, Kanegasaki S. Park MY, et al. Biochem Biophys Res Commun. 1997 May 19;234(2):531-6. doi: 10.1006/bbrc.1997.6672. Biochem Biophys Res Commun. 1997. PMID: 9177307

4

Uncompetitive inhibition of superoxide generation by a synthetic peptide corresponding to a predicted NADPH binding site in gp91-phox, a component of the phagocyte respiratory oxidase.

Tsuchiya T, Imajoh-Ohmi S, Nunoi H, Kanegasaki S. Tsuchiya T, et al. Biochem Biophys Res Commun. 1999 Apr 2;257(1):124-8. doi: 10.1006/bbrc.1999.0428. Biochem Biophys Res Commun. 1999. PMID: 10092521

5

Cell adhesion markedly increases lucigenin-enhanced chemiluminescence of the phagocyte NADPH oxidase.

Kuribayashi F, Tsuruta S, Yamazaki T, Nunoi H, Imajoh-Ohmi S, Kanegasaki S, Nakamura M. Kuribayashi F, et al. Genes Cells. 2008 Dec;13(12):1249-56. doi: 10.1111/j.1365-2443.2008.01241.x. Epub 2008 Nov 19. Genes Cells. 2008. PMID: 19032347 Free article.

6

Characterization of the superoxide-generating system in human peripheral lymphocytes and lymphoid cell lines.

Kobayashi S, Imajoh-Ohmi S, Kuribayashi F, Nunoi H, Nakamura M, Kanegasaki S. Kobayashi S, et al. J Biochem. 1995 Apr;117(4):758-65. doi: 10.1093/oxfordjournals.jbchem.a124773. J Biochem. 1995. PMID: 7592536 Free article.

7

Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients.

Yamada M, Ariga T, Kawamura N, Ohtsu M, Imajoh-Ohmi S, Ohshika E, Tatsuzawa O, Kobayashi K, Sakiyama Y. Yamada M, et al. Br J Haematol. 2000 Mar;108(3):511-7. doi: 10.1046/j.1365-2141.2000.01857.x. Br J Haematol. 2000. PMID: 10759707 Free article.

8

A newly recognized point mutation in the cytochrome b558 heavy chain gene replacing alanine57 by glutamic acid, in a patient with cytochrome b positive X-linked chronic granulomatous disease.

Ariga T, Sakiyama Y, Tomizawa K, Imajoh-Ohmi S, Kanegasaki S, Matsumoto S. Ariga T, et al. Eur J Pediatr. 1993 Jun;152(6):469-72. doi: 10.1007/BF01955051. Eur J Pediatr. 1993. PMID: 8101486

9

Genetic heterogeneity in patients with X-linked recessive chronic granulomatous disease.

Ariga T, Nakanishi M, Tomizawa K, Imajoh-Ohmi S, Kanegasaki S, Sakiyama Y, Matsumoto S. Ariga T, et al. Pediatr Res. 1992 May;31(5):516-9. doi: 10.1203/00006450-199205000-00022. Pediatr Res. 1992. PMID: 1603631

10

A 25-kb deletion in the 5' region of the cytochrome b558 heavy chain gene (CYBB) in a patient with X-linked chronic granulomatous disease.

Faizunnessa NN, Tsuchiya T, Kumatori A, Kurozumi H, Imajoh-Ohmi S, Kanegasaki S, Nakamura M. Faizunnessa NN, et al. Hum Genet. 1997 Apr;99(4):469-73. doi: 10.1007/pl00008702. Hum Genet. 1997. PMID: 9099835

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