Yamazaki H - 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

Mesangial cell-matrix interactions: modulation of matrix expression in mesangial cells by extracellular matrices.

Sakatsume M, Saito A, Takeda T, Yamazaki H, Narita I, Nishi S, Nakagawa Y, Arakawa M. Sakatsume M, et al. Among authors: yamazaki h. Exp Nephrol. 1995 Nov-Dec;3(6):362-8. Exp Nephrol. 1995. PMID: 8528681

3

Molecular genetics of renal diseases.

Saito A, Yamazaki H, Nakagawa Y, Arakawa M. Saito A, et al. Among authors: yamazaki h. Intern Med. 1997 Feb;36(2):81-6. doi: 10.2169/internalmedicine.36.81. Intern Med. 1997. PMID: 9099587 Free article. Review.

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: yamazaki 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

[Molecular genetics of Alport syndrome].

Yamazaki H, Saito A, Nakagawa Y, Arakawa M. Yamazaki H, et al. Nihon Rinsho. 1992 Dec;50(12):3021-6. Nihon Rinsho. 1992. PMID: 1491454 Free article. Review. Japanese.

6

Membranous nephropathy associated with IgG4-related systemic disease and without autoimmune pancreatitis.

Saeki T, Imai N, Ito T, Yamazaki H, Nishi S. Saeki T, et al. Among authors: yamazaki h. Clin Nephrol. 2009 Feb;71(2):173-8. doi: 10.5414/cnp71173. Clin Nephrol. 2009. PMID: 19203510

7

Alternative splicing in the alpha 5(IV) collagen gene in human kidney and skin tissues.

Saito A, Sakatsume M, Yamazaki H, Arakawa M. Saito A, et al. Among authors: yamazaki h. Nihon Jinzo Gakkai Shi. 1994 Jan;36(1):19-24. Nihon Jinzo Gakkai Shi. 1994. PMID: 7509007

8

Down-regulation of interferon-gamma signaling by gene transfer of Stat1 mutant in mesangial cells.

Sakatsume M, Narita I, Yamazaki H, Saito A, Nakagawa Y, Kuriyama H, Kuwano R, Gejyo F, Arakawa M. Sakatsume M, et al. Among authors: yamazaki h. Kidney Int. 2000 Feb;57(2):455-63. doi: 10.1046/j.1523-1755.2000.00865.x. Kidney Int. 2000. PMID: 10652022 Free article.

9

A deletion mutation in the 3' end of the alpha 5(IV) collagen gene in juvenile-onset Alport syndrome.

Saito A, Sakatsume M, Yamazaki H, Ogata F, Hirasawa Y, Arakawa M. Saito A, et al. Among authors: yamazaki h. J Am Soc Nephrol. 1994 Mar;4(9):1649-53. doi: 10.1681/ASN.V491649. J Am Soc Nephrol. 1994. PMID: 8011973

10

MRI-based quantitative assessment of the hippocampal region in very mild to moderate Alzheimer's disease.

Ikeda M, Tanabe H, Nakagawa Y, Kazui H, Oi H, Yamazaki H, Harada K, Nishimura T. Ikeda M, et al. Among authors: yamazaki h. Neuroradiology. 1994;36(1):7-10. doi: 10.1007/BF00599184. Neuroradiology. 1994. PMID: 8108005

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