Nanba E - Search Results

1

Molecular cloning of mouse acid beta-galactosidase cDNA: sequence, expression of catalytic activity and comparison with the human enzyme.

Nanba E, Suzuki K. Nanba E, et al. Biochem Biophys Res Commun. 1990 Nov 30;173(1):141-8. doi: 10.1016/s0006-291x(05)81033-2. Biochem Biophys Res Commun. 1990. PMID: 2124109

2

Expression of the beta-hexosaminidase alpha subunit gene with the four-base insertion of infantile Jewish Tay-Sachs disease.

Nishimoto J, Tanaka A, Nanba E, Suzuki K. Nishimoto J, et al. Among authors: nanba e. J Biol Chem. 1991 Aug 5;266(22):14306-9. J Biol Chem. 1991. PMID: 1830584 Free article.

3

Organization of the mouse acid beta-galactosidase gene.

Nanba E, Suzuki K. Nanba E, et al. Biochem Biophys Res Commun. 1991 Jul 15;178(1):158-64. doi: 10.1016/0006-291x(91)91793-c. Biochem Biophys Res Commun. 1991. PMID: 1906271

4

GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients.

Nishimoto J, Nanba E, Inui K, Okada S, Suzuki K. Nishimoto J, et al. Among authors: nanba e. Am J Hum Genet. 1991 Sep;49(3):566-74. Am J Hum Genet. 1991. PMID: 1909089 Free PMC article.

5

A new point mutation within exon 5 of beta-hexosaminidase alpha gene in a Japanese infant with Tay-Sachs disease.

Nakano T, Nanba E, Tanaka A, Ohno K, Suzuki Y, Suzuki K. Nakano T, et al. Among authors: nanba e. Ann Neurol. 1990 May;27(5):465-73. doi: 10.1002/ana.410270503. Ann Neurol. 1990. PMID: 2141777

6

An autopsy case of G_M1 gangliosidosis type II in a patient who survived a long duration with artificial respiratory support.

Uchino A, Nagai M, Kanazawa N, Ichinoe M, Yanagisawa N, Adachi K, Nanba E, Ishiura H, Mitsui J, Tsuji S, Suzuki K, Murayama S, Nishiyama K. Uchino A, et al. Among authors: nanba e. Neuropathology. 2020 Aug;40(4):379-388. doi: 10.1111/neup.12651. Epub 2020 Mar 27. Neuropathology. 2020. PMID: 32219895

7

Niemann-Pick type C disease: accelerated neurofibrillary tangle formation and amyloid beta deposition associated with apolipoprotein E epsilon 4 homozygosity.

Saito Y, Suzuki K, Nanba E, Yamamoto T, Ohno K, Murayama S. Saito Y, et al. Among authors: nanba e. Ann Neurol. 2002 Sep;52(3):351-5. doi: 10.1002/ana.10266. Ann Neurol. 2002. PMID: 12205649

8

Early-onset, rapidly progressive familial tauopathy with R406W mutation.

Saito Y, Geyer A, Sasaki R, Kuzuhara S, Nanba E, Miyasaka T, Suzuki K, Murayama S. Saito Y, et al. Among authors: nanba e. Neurology. 2002 Mar 12;58(5):811-3. doi: 10.1212/wnl.58.5.811. Neurology. 2002. PMID: 11889249

9

GM1-gangliosidosis: abnormalities in biosynthesis and early processing of beta-galactosidase in fibroblasts.

Nanba E, Tsuji A, Omura K, Suzuki Y. Nanba E, et al. Biochem Biophys Res Commun. 1988 Apr 29;152(2):794-800. doi: 10.1016/s0006-291x(88)80108-6. Biochem Biophys Res Commun. 1988. PMID: 3130055

10

Galactosialidosis: a direct evidence that a 46-kilodalton protein restores deficient enzyme activities in fibroblasts.

Nanba E, Tsuji A, Omura K, Suzuki Y. Nanba E, et al. Biochem Biophys Res Commun. 1987 Apr 14;144(1):138-42. doi: 10.1016/s0006-291x(87)80486-2. Biochem Biophys Res Commun. 1987. PMID: 3107551

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