Fukao T - Search Results

1

Current status of non-invasive prenatal testing in Japan.

Samura O, Sekizawa A, Suzumori N, Sasaki A, Wada S, Hamanoue H, Hirahara F, Sawai H, Nakamura H, Yamada T, Miura K, Masuzaki H, Nakayama S, Okai T, Kamei Y, Namba A, Murotsuki J, Tanemoto T, Fukushima A, Haino K, Tairaku S, Matsubara K, Maeda K, Kaji T, Ogawa M, Osada H, Nishizawa H, Okamoto Y, Kanagawa T, Kakigano A, Kitagawa M, Ogawa M, Izumi S, Katagiri Y, Takeshita N, Kasai Y, Naruse K, Neki R, Masuyama H, Hyodo M, Kawano Y, Ohba T, Ichizuka K, Kido Y, Fukao T, Miharu N, Nagamatsu T, Watanabe A, Hamajima N, Hirose M, Sanui A, Shirato N, Yotsumoto J, Nishiyama M, Hirose T, Sago H. Samura O, et al. Among authors: fukao t. J Obstet Gynaecol Res. 2017 Aug;43(8):1245-1255. doi: 10.1111/jog.13373. Epub 2017 Jun 6. J Obstet Gynaecol Res. 2017. PMID: 28586143

2

Prenatal diagnosis and neonatal monitoring of a fetus with glutaric aciduria type II due to electron transfer flavoprotein (beta-subunit) deficiency.

Yamaguchi S, Shimizu N, Orii T, Fukao T, Suzuki Y, Maeda K, Hashimoto T, Previs SF, Rinaldo P. Yamaguchi S, et al. Among authors: fukao t. Pediatr Res. 1991 Nov;30(5):439-43. doi: 10.1203/00006450-199111000-00009. Pediatr Res. 1991. PMID: 1754299

3

Effect of Hunter disease (mucopolysaccharidosis type II) mutations on molecular phenotypes of iduronate-2-sulfatase: enzymatic activity, protein processing and structural analysis.

Sukegawa-Hayasaka K, Kato Z, Nakamura H, Tomatsu S, Fukao T, Kuwata K, Orii T, Kondo N. Sukegawa-Hayasaka K, et al. Among authors: fukao t. J Inherit Metab Dis. 2006 Dec;29(6):755-61. doi: 10.1007/s10545-006-0440-7. Epub 2006 Nov 7. J Inherit Metab Dis. 2006. PMID: 17091340

4

Biochemical and immunochemical study of seven families with 3-ketothiolase deficiency: diagnosis of heterozygotes using immunochemical determination of the ratio of mitochondrial acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase proteins.

Yamaguchi S, Sakai A, Fukao T, Wakazono A, Kuwahara T, Orii T, Hashimoto T. Yamaguchi S, et al. Among authors: fukao t. Pediatr Res. 1993 May;33(5):429-32. doi: 10.1203/00006450-199305000-00001. Pediatr Res. 1993. PMID: 8099727

5

Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiency.

Fukao T, Song XQ, Watanabe H, Hirayama K, Sakazaki H, Shintaku H, Imanaka M, Orii T, Kondo N. Fukao T, et al. Prenat Diagn. 1996 May;16(5):471-4. doi: 10.1002/(SICI)1097-0223(199605)16:5<471::AID-PD898>3.0.CO;2-E. Prenat Diagn. 1996. PMID: 8844009

6

Identification of three mutant alleles of the gene for mitochondrial acetoacetyl-coenzyme A thiolase. A complete analysis of two generations of a family with 3-ketothiolase deficiency.

Fukao T, Yamaguchi S, Orii T, Schutgens RB, Osumi T, Hashimoto T. Fukao T, et al. J Clin Invest. 1992 Feb;89(2):474-9. doi: 10.1172/JCI115608. J Clin Invest. 1992. PMID: 1346617 Free PMC article.

7

Chromosome mapping of the human mitochondrial acetoacetyl-coenzyme A thiolase gene to 11q22.3----q23.1 by fluorescence in situ hybridization.

Masuno M, Kano M, Fukao T, Yamaguchi S, Osumi T, Hashimoto T, Takahashi E, Hori T, Orii T. Masuno M, et al. Among authors: fukao t. Cytogenet Cell Genet. 1992;60(2):121-2. doi: 10.1159/000133319. Cytogenet Cell Genet. 1992. PMID: 1351831 No abstract available.

8

Molecular basis of 3-ketothiolase deficiency: detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolase.

Fukao T, Yamaguchi S, Wakazono A, Okamoto H, Orii T, Osumi T, Hashimoto T. Fukao T, et al. J Inherit Metab Dis. 1992;15(5):815-20. doi: 10.1007/BF01800027. J Inherit Metab Dis. 1992. PMID: 1359192 No abstract available.

9

Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiency.

Yamaguchi S, Fukao T, Kano M, Wakazono A, Orii T, Sakura N, Hashimoto T. Yamaguchi S, et al. Among authors: fukao t. Tohoku J Exp Med. 1992 Jun;167(2):143-53. doi: 10.1620/tjem.167.143. Tohoku J Exp Med. 1992. PMID: 1362011 Free article.

10

Identification of TaqI polymorphism in the mitochondrial acetoacetyl-CoA thiolase gene and familial analysis of 3-ketothiolase deficiency.

Kuwahara T, Fukao T, Kano M, Yamaguchi S, Orii T, Hashimoto T. Kuwahara T, et al. Among authors: fukao t. Hum Genet. 1992 Nov;90(3):208-10. doi: 10.1007/BF00220063. Hum Genet. 1992. PMID: 1362557

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