Tsukamoto T - Search Results

1

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

2

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Fujiki Y. Shimozawa N, et al. Among authors: tsukamoto t. J Clin Invest. 1992 Nov;90(5):1864-70. doi: 10.1172/JCI116063. J Clin Invest. 1992. PMID: 1430210 Free PMC article.

We previously isolated two Chinese hamster ovary (CHO) cell mutants (Z24 and Z65) that resemble the fibroblasts from patients with such diseases, in their defective peroxisome assembly (Tsukamoto, T., S. Yokota, and Y. Fujiki. 1990. J. Cell Biol. 110:651-660). Here …

We previously isolated two Chinese hamster ovary (CHO) cell mutants (Z24 and Z65) that resemble the fibroblasts from patients with such dise …

3

A human gene responsible for Zellweger syndrome that affects peroxisome assembly.

Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Shirayoshi Y, Mori T, Fujiki Y. Shimozawa N, et al. Among authors: tsukamoto t. Science. 1992 Feb 28;255(5048):1132-4. doi: 10.1126/science.1546315. Science. 1992. PMID: 1546315

4

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

5

Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.

Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T. Shimozawa N, et al. Among authors: tsukamoto t. Pediatr Res. 1996 May;39(5):812-5. doi: 10.1203/00006450-199605000-00011. Pediatr Res. 1996. PMID: 8726233

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

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

8

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.

9

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

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,344 results

Search Page

Filters