Kominami E - Search Results

1

The intracellular location and function of proteins of neuronal ceroid lipofuscinoses.

Ezaki J, Kominami E. Ezaki J, et al. Among authors: kominami e. Brain Pathol. 2004 Jan;14(1):77-85. doi: 10.1111/j.1750-3639.2004.tb00501.x. Brain Pathol. 2004. PMID: 14997940 Free PMC article. Review.

2

Characterization of Cln3p, the gene product responsible for juvenile neuronal ceroid lipofuscinosis, as a lysosomal integral membrane glycoprotein.

Ezaki J, Takeda-Ezaki M, Koike M, Ohsawa Y, Taka H, Mineki R, Murayama K, Uchiyama Y, Ueno T, Kominami E. Ezaki J, et al. Among authors: kominami e. J Neurochem. 2003 Dec;87(5):1296-308. doi: 10.1046/j.1471-4159.2003.02132.x. J Neurochem. 2003. PMID: 14622109 Free article.

3

CLC-3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis.

Yoshikawa M, Uchida S, Ezaki J, Rai T, Hayama A, Kobayashi K, Kida Y, Noda M, Koike M, Uchiyama Y, Marumo F, Kominami E, Sasaki S. Yoshikawa M, et al. Among authors: kominami e. Genes Cells. 2002 Jun;7(6):597-605. doi: 10.1046/j.1365-2443.2002.00539.x. Genes Cells. 2002. PMID: 12059962 Free article.

4

Abnormal degradative pathway of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid-lipofuscinosis (Batten disease).

Ezaki J, Wolfe LS, Ishidoh K, Kominami E. Ezaki J, et al. Among authors: kominami e. Am J Med Genet. 1995 Jun 5;57(2):254-9. doi: 10.1002/ajmg.1320570229. Am J Med Genet. 1995. PMID: 7668341 Review.

5

Specific delay of degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis (Batten disease).

Ezaki J, Wolfe LS, Higuti T, Ishidoh K, Kominami E. Ezaki J, et al. Among authors: kominami e. J Neurochem. 1995 Feb;64(2):733-41. doi: 10.1046/j.1471-4159.1995.64020733.x. J Neurochem. 1995. PMID: 7830067

6

Molecular basis of lysosomal accumulation of subunit c of mitochondrial ATP synthase in neuronal ceroid-lipofuscinosis.

Ezaki J, Wolfe LS, Kominami E. Ezaki J, et al. Among authors: kominami e. J Inherit Metab Dis. 1993;16(2):296-8. doi: 10.1007/BF00710269. J Inherit Metab Dis. 1993. PMID: 8411985 Review. No abstract available.

7

[Batten disease (Neuronal ceroid lipofuscinoses)--accumulation of ATP synthase subunit c caused by the delay of lysosomal degradation].

Ezaki J, Kominami E. Ezaki J, et al. Among authors: kominami e. Nihon Rinsho. 1995 Dec;53(12):3055-61. Nihon Rinsho. 1995. PMID: 8577058 Review. Japanese.

8

New insight into lysosomal protein storage disease: delayed catabolism of ATP synthase subunit c in Batten disease.

Kominami E, Ezaki J, Wolfe LS. Kominami E, et al. Neurochem Res. 1995 Nov;20(11):1305-9. doi: 10.1007/BF00992505. Neurochem Res. 1995. PMID: 8786816 Review.

9

Defect of proteolysis of mitochondrial ATP synthase subunit C in neuronal ceroid lipofuscinosis.

Ezaki J, Wolfe LS, Kominami E. Ezaki J, et al. Among authors: kominami e. Gerontology. 1995;41 Suppl 2:259-69. doi: 10.1159/000213748. Gerontology. 1995. PMID: 8821337

10

Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit c.

Ezaki J, Wolfe LS, Kominami E. Ezaki J, et al. Among authors: kominami e. J Neurochem. 1996 Oct;67(4):1677-87. doi: 10.1046/j.1471-4159.1996.67041677.x. J Neurochem. 1996. PMID: 8858953

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