Suzuki Y - Search Results

1

Carbamyl phosphate synthetase I deficiency with no detectable mRNA activity.

Suzuki Y, Matsushima A, Ohtake A, Mori M, Tatibana M, Orii T. Suzuki Y, et al. Eur J Pediatr. 1986 Oct;145(5):406-8. doi: 10.1007/BF00439249. Eur J Pediatr. 1986. PMID: 3792387

2

Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.

Suzuki Y, Shimozawa N, Orii T, Igarashi N, Kono N, Matsui A, Inoue Y, Yokota S, Hashimoto T. Suzuki Y, et al. J Pediatr. 1988 Nov;113(5):841-5. doi: 10.1016/s0022-3476(88)80011-8. J Pediatr. 1988. PMID: 3183838

3

Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome.

Suzuki Y, Orii T, Mori M, Tatibana M, Hashimoto T. Suzuki Y, et al. Clin Chim Acta. 1986 Apr 30;156(2):191-6. doi: 10.1016/0009-8981(86)90152-x. Clin Chim Acta. 1986. PMID: 3519003

4

Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.

Suzuki Y, Shimozawa N, Orii T, Igarashi N, Kono N, Hashimoto T. Suzuki Y, et al. Clin Chim Acta. 1988 Feb 29;172(1):65-76. doi: 10.1016/0009-8981(88)90121-0. Clin Chim Acta. 1988. PMID: 2452040

5

Biosynthesis of membrane polypeptides of rat liver peroxisomes.

Suzuki Y, Orii T, Takiguchi M, Mori M, Hijikata M, Hashimoto T. Suzuki Y, et al. J Biochem. 1987 Feb;101(2):491-6. doi: 10.1093/oxfordjournals.jbchem.a121935. J Biochem. 1987. PMID: 3584097 Free article.

6

Biosynthesis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome.

Suzuki Y, Orii T, Hashimoto T. Suzuki Y, et al. J Inherit Metab Dis. 1986;9(3):292-6. doi: 10.1007/BF01799668. J Inherit Metab Dis. 1986. PMID: 3099077 No abstract available.

7

Molecular analysis of holocarboxylase synthetase deficiency: a missense mutation and a single base deletion are predominant in Japanese patients.

Aoki Y, Suzuki Y, Sakamoto O, Li X, Takahashi K, Ohtake A, Sakuta R, Ohura T, Miyabayashi S, Narisawa K. Aoki Y, et al. Among authors: suzuki y. Biochim Biophys Acta. 1995 Dec 12;1272(3):168-74. doi: 10.1016/0925-4439(95)00082-8. Biochim Biophys Acta. 1995. PMID: 8541348 Free article.

8

Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group.

Poulos A, Christodoulou J, Chow CW, Goldblatt J, Paton BC, Orii T, Suzuki Y, Shimozawa N. Poulos A, et al. Among authors: suzuki y. J Pediatr. 1995 Oct;127(4):596-9. doi: 10.1016/s0022-3476(95)70121-4. J Pediatr. 1995. PMID: 7562283

9

Cloning and sequence analysis of a full length cDNA encoding human mitochondrial 3-oxoacyl-CoA thiolase.

Abe H, Ohtake A, Yamamoto S, Satoh Y, Takayanagi M, Amaya Y, Takiguchi M, Sakuraba H, Suzuki Y, Mori M, et al. Abe H, et al. Among authors: suzuki y. Biochim Biophys Acta. 1993 Nov 16;1216(2):304-6. doi: 10.1016/0167-4781(93)90160-f. Biochim Biophys Acta. 1993. PMID: 8241273

10

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.

Suzuki Y, Jiang LL, Souri M, Miyazawa S, Fukuda S, Zhang Z, Une M, Shimozawa N, Kondo N, Orii T, Hashimoto T. Suzuki Y, et al. Am J Hum Genet. 1997 Nov;61(5):1153-62. doi: 10.1086/301599. Am J Hum Genet. 1997. PMID: 9345094 Free PMC article.

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