Tsukamoto T - Search Results

1

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.

Imamura A, Tsukamoto T, Shimozawa N, Suzuki Y, Zhang Z, Imanaka T, Fujiki Y, Orii T, Kondo N, Osumi T. Imamura A, et al. Among authors: tsukamoto t. Am J Hum Genet. 1998 Jun;62(6):1539-43. doi: 10.1086/301881. Am J Hum Genet. 1998. PMID: 9585609 Free PMC article. No abstract available.

2

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.

Imamura A, Tamura S, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Orii T, Kondo N, Osumi T, Fujiki Y. Imamura A, et al. Among authors: tsukamoto t. Hum Mol Genet. 1998 Dec;7(13):2089-94. doi: 10.1093/hmg/7.13.2089. Hum Mol Genet. 1998. PMID: 9817926

3

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Kondo N, Kinoshita N, Fujiki Y, Tsukamoto T, Osumi T, Imanaka T, Orii T, Beemer F, Mooijer P, Dekker C, Wanders RJ. Shimozawa N, et al. Among authors: tsukamoto t. Am J Hum Genet. 1998 Dec;63(6):1898-903. doi: 10.1086/302142. Am J Hum Genet. 1998. PMID: 9837841 Free PMC article. No abstract available.

4

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Toyama R, Mukai S, Fujiki Y, Tsukamoto T, Osumi T, Orii T, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: tsukamoto t. Hum Mol Genet. 1999 Jun;8(6):1077-83. doi: 10.1093/hmg/8.6.1077. Hum Mol Genet. 1999. PMID: 10332040

5

Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant.

Tsukamoto T, Miura S, Nakai T, Yokota S, Shimozawa N, Suzuki Y, Orii T, Fujiki Y, Sakai F, Bogaki A, Yasumo H, Osumi T. Tsukamoto T, et al. Nat Genet. 1995 Dec;11(4):395-401. doi: 10.1038/ng1295-395. Nat Genet. 1995. PMID: 7493019

6

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

Fukuda S, Shimozawa N, Suzuki Y, Zhang Z, Tomatsu S, Tsukamoto T, Hashiguchi N, Osumi T, Masuno M, Imaizumi K, Kuroki Y, Fujiki Y, Orii T, Kondo N. Fukuda S, et al. Among authors: tsukamoto t. Am J Hum Genet. 1996 Dec;59(6):1210-20. Am J Hum Genet. 1996. PMID: 8940266 Free PMC article.

7

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.

Tateishi K, Okumoto K, Shimozawa N, Tsukamoto T, Osumi T, Suzuki Y, Kondo N, Okano I, Fujiki Y. Tateishi K, et al. Among authors: tsukamoto t. Eur J Cell Biol. 1997 Aug;73(4):352-9. Eur J Cell Biol. 1997. PMID: 9270878

8

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Tsukamoto T, Osumi T, Tateishi K, Okumoto K, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: tsukamoto t. Biochem Biophys Res Commun. 1998 Feb 13;243(2):368-71. doi: 10.1006/bbrc.1997.8067. Biochem Biophys Res Commun. 1998. PMID: 9480815

9

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.

Zhang Z, Suzuki Y, Shimozawa N, Fukuda S, Imamura A, Tsukamoto T, Osumi T, Fujiki Y, Orii T, Wanders RJ, Barth PG, Moser HW, Paton BC, Besley GT, Kondo N. Zhang Z, et al. Among authors: tsukamoto t. Hum Mutat. 1999;13(6):487-96. doi: 10.1002/(SICI)1098-1004(1999)13:6<487::AID-HUMU9>3.0.CO;2-T. Hum Mutat. 1999. PMID: 10408779

10

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.

Shimozawa N, Imamura A, Zhang Z, Suzuki Y, Orii T, Tsukamoto T, Osumi T, Fujiki Y, Wanders RJ, Besley G, Kondo N. Shimozawa N, et al. Among authors: tsukamoto t. J Med Genet. 1999 Oct;36(10):779-81. doi: 10.1136/jmg.36.10.779. J Med Genet. 1999. PMID: 10528859 Free PMC article.

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