Nunoi H - Search Results

1

A new mutation in exon 12 of the gp91-phox gene leading to cytochrome b-positive X-linked chronic granulomatous disease.

Azuma H, Oomi H, Sasaki K, Kawabata I, Sakaino T, Koyano S, Suzutani T, Nunoi H, Okuno A. Azuma H, et al. Among authors: nunoi h. Blood. 1995 Jun 1;85(11):3274-7. Blood. 1995. PMID: 7756659 Free article.

2

[Molecular bases of chronic granulomatous disease--analysis of the involvement of cytosol factors for NADPH oxidase].

Nunoi H, Matsuda I. Nunoi H, et al. Rinsho Byori. 1992 Apr;40(4):380-4. Rinsho Byori. 1992. PMID: 1317471 Review. Japanese.

We analyzed cytosol components with column method, and clarified that 3 neutrophil cytosol factors (NCF-1/-2/-3) was necessary for reconstitute the cytosol activity which was missing in an autosomal recessive type of Chronic Granulomatous Disease (CGD) patients (Nunoi H …

We analyzed cytosol components with column method, and clarified that 3 neutrophil cytosol factors (NCF-1/-2/-3) was necessary for reconstit …

3

AG dinucleotide insertion in a patient with chronic granulomatous disease lacking cytosolic 67-kD protein.

Nunoi H, Iwata M, Tatsuzawa S, Onoe Y, Shimizu S, Kanegasaki S, Matsuda I. Nunoi H, et al. Blood. 1995 Jul 1;86(1):329-33. Blood. 1995. PMID: 7795241 Free article.

4

Homologous dinucleotide (GT or TG) deletion in Japanese patients with chronic granulomatous disease with p47-phox deficiency.

Iwata M, Nunoi H, Yamazaki H, Nakano T, Niwa H, Tsuruta S, Ohga S, Ohmi S, Kanegasaki S, Matsuda I. Iwata M, et al. Among authors: nunoi h. Biochem Biophys Res Commun. 1994 Mar 30;199(3):1372-7. doi: 10.1006/bbrc.1994.1382. Biochem Biophys Res Commun. 1994. PMID: 8147881

5

Two-exon skipping due to a point mutation in p67-phox--deficient chronic granulomatous disease.

Aoshima M, Nunoi H, Shimazu M, Shimizu S, Tatsuzawa O, Kenney RT, Kanegasaki S. Aoshima M, et al. Among authors: nunoi h. Blood. 1996 Sep 1;88(5):1841-5. Blood. 1996. PMID: 8781442 Free article.

6

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. Among authors: nunoi h. 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.

7

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. Among authors: nunoi h. Biochem Biophys Res Commun. 1999 Apr 2;257(1):124-8. doi: 10.1006/bbrc.1999.0428. Biochem Biophys Res Commun. 1999. PMID: 10092521

8

[Statistical evaluation of chronic granulomatous disease in Japan and basic studies for gene therapy for CGD patients].

Nunoi H, Ishibashi F. Nunoi H, et al. Rinsho Byori. 1999 Jul;47(7):658-64. Rinsho Byori. 1999. PMID: 10442045 Japanese.

9

[Gene therapy for inherited diseases using heamatopoietic stem cells--gene therapy for patients with chronic granulomatous disease].

Nunoi H, Ishibashi F. Nunoi H, et al. Hum Cell. 1999 Sep;12(3):103-8. Hum Cell. 1999. PMID: 10695016 Review. Japanese.

10

Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiency.

Ishibashi F, Nunoi H, Endo F, Matsuda I, Kanegasaki S. Ishibashi F, et al. Among authors: nunoi h. Hum Genet. 2000 May;106(5):473-81. doi: 10.1007/s004390000288. Hum Genet. 2000. PMID: 10914676

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