Matsuda I - Search Results

1

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: matsuda i. Biochem Biophys Res Commun. 1994 Mar 30;199(3):1372-7. doi: 10.1006/bbrc.1994.1382. Biochem Biophys Res Commun. 1994. PMID: 8147881

2

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: matsuda i. Hum Genet. 2000 May;106(5):473-81. doi: 10.1007/s004390000288. Hum Genet. 2000. PMID: 10914676

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. Among authors: matsuda i. Blood. 1995 Jul 1;86(1):329-33. Blood. 1995. PMID: 7795241 Free article.

4

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

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

5

Drug-selected complete restoration of superoxide generation in Epstein-Barr virus-transformed B cells from p47phox-deficient chronic granulomatous disease patients by using a bicistronic retrovirus vector encoding a human multi-drug resistance gene (MDR1) and the p47phox gene.

Iwata M, Nunoi H, Matsuda I, Kanegasaki S, Tsuruo T, Sugimoto Y. Iwata M, et al. Among authors: matsuda i. Hum Genet. 1998 Oct;103(4):419-23. doi: 10.1007/s004390050844. Hum Genet. 1998. PMID: 9856484

6

Combination of arachidonic acid and guanosine 5'-O-(3-thiotriphosphate) induce translocation of rac p21s to membrane and activation of NADPH oxidase in a cell-free system.

Sawai T, Asada M, Nunoi H, Matsuda I, Ando S, Sasaki T, Kaibuchi K, Takai Y, Katayama K. Sawai T, et al. Among authors: matsuda i. Biochem Biophys Res Commun. 1993 Aug 31;195(1):264-9. doi: 10.1006/bbrc.1993.2039. Biochem Biophys Res Commun. 1993. PMID: 8395827

7

Leukocyte adhesion deficiency: identification of novel mutations in two Japanese patients with a severe form.

Matsuura S, Kishi F, Tsukahara M, Nunoi H, Matsuda I, Kobayashi K, Kajii T. Matsuura S, et al. Among authors: matsuda i. Biochem Biophys Res Commun. 1992 May 15;184(3):1460-7. doi: 10.1016/s0006-291x(05)80047-6. Biochem Biophys Res Commun. 1992. PMID: 1590804

8

A heterozygous mutation of beta-actin associated with neutrophil dysfunction and recurrent infection.

Nunoi H, Yamazaki T, Tsuchiya H, Kato S, Malech HL, Matsuda I, Kanegasaki S. Nunoi H, et al. Among authors: matsuda i. Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8693-8. doi: 10.1073/pnas.96.15.8693. Proc Natl Acad Sci U S A. 1999. PMID: 10411937 Free PMC article.

9

[Neutropenia in patient with X-linked hyper-IgM syndrome].

Iwata M, Nunoi H, Nonoyama S, Shimadzu M, Higuchi S, Yanabe Y, Migita M, Adachi N, Matsuda I. Iwata M, et al. Among authors: matsuda i. Rinsho Ketsueki. 1995 Oct;36(10):1223-9. Rinsho Ketsueki. 1995. PMID: 8531335 Japanese.

10

[NADPH oxidase and cell membrane].

Nunoi H, Matsuda I. Nunoi H, et al. Among authors: matsuda i. Rinsho Byori. 1991 Sep;Suppl 91:140-9. Rinsho Byori. 1991. PMID: 1661787 Japanese. No abstract available.

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