Imamura A - Search Results

1

[Newly identified peroxisomal disorders].

Suzuki Y, Shimozawa N, Imamura A, Zhang Z, Kondo N. Suzuki Y, et al. Among authors: imamura a. No To Shinkei. 1999 Apr;51(4):295-302. No To Shinkei. 1999. PMID: 10363263 Review. Japanese. No abstract available.

2

Immunohistochemistry for a bifunctional protein in patients with peroxisomal disorders.

Imamura A, Kamei A, Suzuki Y, Kondo N, Orii T, Takashima S. Imamura A, et al. Pediatr Neurol. 1995 May;12(4):341-5. doi: 10.1016/0887-8994(95)00053-i. Pediatr Neurol. 1995. PMID: 7546007

3

Peroxisomal disorders: clinical aspects.

Suzuki Y, Shimozawa N, Takahashi Y, Imamura A, Kondo N, Orii T. Suzuki Y, et al. Among authors: imamura a. Ann N Y Acad Sci. 1996 Dec 27;804:442-9. doi: 10.1111/j.1749-6632.1996.tb18635.x. Ann N Y Acad Sci. 1996. PMID: 8993563

4

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. Hum Mol Genet. 1998 Dec;7(13):2089-94. doi: 10.1093/hmg/7.13.2089. Hum Mol Genet. 1998. PMID: 9817926

5

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: imamura a. 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

6

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: imamura a. 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.

7

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.

Imamura A, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Fujiki Y, Orii T, Osumi T, Kondo N. Imamura A, et al. Brain Dev. 2000 Jan;22(1):8-12. doi: 10.1016/s0387-7604(99)00072-8. Brain Dev. 2000. PMID: 10761827

8

Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.

Imamura A, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Fujiki Y, Orii T, Osumi T, Wanders RJ, Kondo N. Imamura A, et al. Pediatr Res. 2000 Oct;48(4):541-5. doi: 10.1203/00006450-200010000-00020. Pediatr Res. 2000. PMID: 11004248

9

[Peroxisomal disorders].

Suzuki Y, Shimozawa N, Imamura A, Kondo N. Suzuki Y, et al. Among authors: imamura a. Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):452-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11031991 Review. Japanese. No abstract available.

10

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: imamura a. Biochem Biophys Res Commun. 1998 Feb 13;243(2):368-71. doi: 10.1006/bbrc.1997.8067. Biochem Biophys Res Commun. 1998. PMID: 9480815

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

578 results

Search Page

Filters