FUKAO Toshiyuki

J-GLOBAL         Last updated: Jul 2, 2019 at 02:42
 
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Name
FUKAO Toshiyuki
Affiliation
Gifu University
Section
Graduate School of Medicine
Degree
(BLANK)(Gifu University)

Research Areas

 
 

Academic & Professional Experience

 
Nov 2013
 - 
Today
Professor, Department of Pediatrics, Gifu University Graduate School of Medicine
 
Apr 2007
 - 
Oct 2013
Professor, Gifu University Graduate School of Medicine
 

Education

 
 
 - 
1985
Faculty of Medicine, Mie University
 
 
 - 
1989
Graduate School, Division of Medicine, Gifu University
 

Published Papers

 
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase.
Fukao T, Kamijo K, Osumi T, Fujiki Y, Yamaguchi S, Orii T, Hashimoto T
Journal of biochemistry   106(2) 197-204   Aug 1989   [Refereed]
Fukao T, Yamaguchi S, Kano M, Orii T, Fujiki Y, Osumi T, Hashimoto T
The Journal of clinical investigation   86(6) 2086-2092   Dec 1990   [Refereed]
Fukao T, Yamaguchi S, Tomatsu S, Orii T, Frauendienst-Egger G, Schrod L, Osumi T, Hashimoto T
Biochemical and biophysical research communications   179(1) 124-129   Aug 1991   [Refereed]
Yamaguchi S, Shimizu N, Orii T, Fukao T, Suzuki Y, Maeda K, Hashimoto T, Previs SF, Rinaldo P
Pediatric research   30(5) 439-443   Nov 1991   [Refereed]
Tomatsu S, Fukuda S, Masue M, Sukegawa K, Fukao T, Yamagishi A, Hori T, Iwata H, Ogawa T, Nakashima Y
Biochemical and biophysical research communications   181(2) 677-683   Dec 1991   [Refereed]
Structure and expression of the human mitochondrial acetoacetyl-CoA thiolase-encoding gene.
Kano M, Fukao T, Yamaguchi S, Orii T, Osumi T, Hashimoto T
Gene   109(2) 285-290   Dec 1991   [Refereed]
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetyl-coenzyme-A thiolase.
Wajner M, Sanseverino MT, Giugliani R, Sweetman L, Yamaguchi S, Fukao T, Shih VE
Clin Genet   41 202-205   1992   [Refereed]
Masuno M, Kano M, Fukao T, Yamaguchi S, Osumi T, Hashimoto T, Takahashi E, Hori T, Orii T
Cytogenetics and cell genetics   60(2) 121-122   1992   [Refereed]
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
Journal of inherited metabolic disease   15(5) 815-820   1992   [Refereed]
Fukao T, Yamaguchi S, Orii T, Schutgens RB, Osumi T, Hashimoto T
The Journal of clinical investigation   89(2) 474-479   Feb 1992   [Refereed]
Yamaguchi S, Fukao T, Kano M, Wakazono A, Orii T, Sakura N, Hashimoto T
The Tohoku journal of experimental medicine   167(2) 143-153   Jun 1992   [Refereed]
Molecular basis of 3-ketothiolase deficiency: identification of an AG to AC substitution at the splice acceptor site of intron 10 causing exon 11 skipping.
Fukao T, Yamaguchi S, Orii T, Osumi T, Hashimoto T
Biochimica et biophysica acta   1139(3) 184-188   Jul 1992   [Refereed]
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
Human genetics   90(3) 208-210   Nov 1992   [Refereed]
Fukao T, Yamaguchi S, Scriver CR, Dunbar G, Wakazono A, Kano M, Orii T, Hashimoto T
Human mutation   2(3) 214-220   1993   [Refereed]
Ambrose HJ, Byrd PJ, McConvile CM, Cooper PR, Stankovic T, Riley JH, Shiloh Y, McNamara JO, Fukao T, Taylor MR
Genomics   21 612-619   1994   [Refereed]
Song X-Q, Fukao T, Yamaguchi S, Miyazawa S, Hashimoto T, Orii T
Biochem Biophys Res Commun   201 478-487   1994   [Refereed]
Uchiyama A, Suzuki Y, Song XQ, Fukao T, Imamura A, Tomatsu S, Shimozawa N, Kondo N, Orii T
Biochemical and biophysical research communications   198(2) 632-636   Jan 1994   [Refereed]
Fukao T, Yamaguchi S, Wakazono A, Orii T, Hoganson G, Hashimoto T
The Journal of clinical investigation   93(3) 1035-1041   Mar 1994   [Refereed]
A new Japanese case of succinyl-CoA:3-ketoacid CoA-transferase deficiency.
Sakazaki H, Hirayama K, Murakami S, Yonezawa S, Shintaku H, Sawada Y, Fukao T, Watanabe H, Orii T, Isshiki G
J Inherit Metab Dis   18 323-325   1995   [Refereed]
Sukegawa K, Tomatsu S, Fukao T, Iwata H, Song XQ, Yamada Y, Fukuda S, Isogai K, Orii T
Human mutation   6(2) 136-143   1995   [Refereed]
Wakazono A, Fukao T, Yamaguchi S, Hori T, Orii T, Lambert M, Mitchell GA, Lee GW, Hashimoto T
Human mutation   5(1) 34-42   1995   [Refereed]
Fukao T, Song XQ, Yamaguchi S, Orii T, Wanders RJ, Poll-The BT, Hashimoto T
Human mutation   5(1) 94-96   1995   [Refereed]
Fukao T, Yamaguchi S, Orii T, Hashimoto T
Human mutation   5(2) 113-120   1995   [Refereed]
Prenatal Diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection method.
Fukao T, Wakazono A, Song XQ, Yamaguchi S, Zacharias R, Donlan MA, Orii T
Prenatal diagnosis   15(4) 363-367   Apr 1995   [Refereed]
Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient.
Song XQ, Fukao T, Suzuki Y, Imamura A, Uchiyama A, Shimozawa N, Kondo N, Orii T
Human molecular genetics   4(6) 1093-1094   Jun 1995   [Refereed]
Identification of the D-enantiomer of 2-hydroxyglutaric acid in glutaric aciduria type II.
Watanabe H, Yamaguchi S, Saiki K, Shimizu N, Fukao T, Kondo N, Orii T
Clinica chimica acta; international journal of clinical chemistry   238(2) 115-124   Jul 1995   [Refereed]
Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytes.
Fukao T, Kodama K, Aoyanagi N, Tsukino R, Uemura S, Song X-Q,Watanabe H, Kuhara T, Orii T, Kondo N
Clin Genet   50 263-266   1996   [Refereed]
High sensitivity and specificity of proliferative response of lymphocytes to food antigens for detection of the offending food in patients with food-sensitive atopic dermatitis. Pediatric Asthma,
Kondo N, Kaneko H, Fukao T, Inoue R, Teramoto T, Tashita H, Yokoyama Y
Allergy and Immunology   10 175-180   1996   [Refereed]
Kaneko H, Inoue R, Yamada Y, Sukegawa K, Fukao T, Tashita H, Teramoto T, Kasahara K, Takami T, Kondo N
Int J Cancer (Pred Oncol)   69 480-483   1996   [Refereed]
Pecker I, Avraham KB, Gilbert DJ, Savitsky K,Rotman G, Harnik R, Fukao T, Schrock E, Hirotsune S, Tagle D, Collins FS, Wynshaw-Boris A, Ried T, Copeland NG, Jenkins NA, Shiloh Y,Ziv Y
Genomics   35 39-45   1996   [Refereed]
Assignment of the mouse ataxia-telangiectasia gene (atm) to mouse chromosome 9.
Xia V-R, Welch CL,Warden CH, Lange E, Fukao T, Lusis AJ, Gatti GA
Mammalian Genome   7 554-555   1996   [Refereed]
Comparative genome mapping of the ataxia-telangiectasia region in mouse, rat, and syrian hamster. Genomics 34:347-352, 1996
Matsuda Y, Imai T, Shiomi T, Saito T, Yamauchi M, Fukao T, Akao Y, Seki N, Ito H, Hori T
Genomics   34 347-352   1996   [Refereed]
Association between FcεRIβ and atopic disorder in Japanese population?
Fukao T, Kaneko H, Teramoto T, Tashita H, Kondo N
Lancet   348 407   1996   [Refereed]
Succinyl CoA:3-Oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.
Kassovska-Bratinoba S, Fukao T, Song X-Q,Duncan AMY, Chen HC, Robert M-F, Perez-Cerda C, Ugarte M, Chartrand P, Vobecky S, Kondo N, Mitchell GA
Am J Hum Genet   59 519-528   1996   [Refereed]
Masuno M, Fukao T, Song X-Q,Yamaguchi S,Orii T, Kondo N, Imaizumi K, Kuroki Y
Genomics   36 217-218   1996   [Refereed]
Imamura A, Suzuki S, Song X-Q, Fukao T, Shimozawa N, Orii T, Kondo N
Prenatal Diagnosis   16 259-261   1996   [Refereed]
Fukao T, Song X-Q, Watanabe H, Hirayama K, Sakazaki H, Shintaku H, Imanaka M,Orii T, Kondo N
Prenatal Diagnosis   16 471-474   1996   [Refereed]
Fukao T, Song XQ, Yamaguchi S, Hashimoto T, Orii T, Kondo N
Pediatric research   39(6) 1055-1058   Jun 1996   [Refereed]
Life-threatening cardiac involvement throughout life in a case of Costello syndrome.
Fukao T, Sakai S, Shimozawa N, Kuwahara T, Kano M, Goto E, Nakashima Y, Katagiri-Kawade M, Ichihashi H, Masuno M, Orii T, Kondo N
Clinical genetics   50(4) 244-247   Oct 1996   [Refereed]
Kaneko H, Orii KO, Matsui E, Shimozawa N, Fukao T, Matsumoto T, Shimamoto A, Furuichi Y, Hayakawa S, Kasahara K, Kondo N
Biochem Biophys Res Commun   240 348-353   1997   [Refereed]
Sukegawa K, Song XQ, Masuno M, Fukao T, Shimozawa N, Fukuda S, Isogai K, Nishio H,Matsuo M, Tomatsu S, Kondo N, Orii T
Hum Mutat   10 361-367   1997   [Refereed]
Management of malignant lymphoma in two siblings with Bloom's syndrome.
Kaneko H, Inoue R, Yamada Y, Fukao T, Kondo N
Oncology Reports   4 1281-1283   1997   [Refereed]
Reduced expression of the interferon-gamma messenger RNA in IgG2 deficiency.
Kondo N, Inoue R, Kasahara K, Fukao T, Kaneko H, Tashita H, Teramoto T
Scandinavian journal of immunology   45(2) 227-230   Feb 1997   [Refereed]
Song XQ, Fukao T, Mitchell GA, Kassovska-Bratinova S, Ugarte M, Wanders RJ, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N
Biochimica et biophysica acta   1360(2) 151-156   Apr 1997   [Refereed]
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients.
Imamura A, Suzuki Y, Song XQ, Fukao T, Uchiyama A, Shimozawa N, Kamijo K, Hashimoto T, Orii T, Kondo N
Clinical genetics   51(5) 322-325   May 1997   [Refereed]
Inhibition of interferon-gamma production from lymphocytes stimulated with food antigens by a beta 2-agonist, procaterol, in patients with food-sensitive atopic dermatitis.
Kondo N, Shinbara M, Inoue R, Fukao T, Kaneko H, Teramoto T, Tashita H
Journal of investigational allergology & clinical immunology   7(4) 225-228   Jul 1997   [Refereed]
Fukao T, Song XQ, Mitchell GA, Yamaguchi S, Sukegawa K, Orii T, Kondo N
Pediatric research   42(4) 498-502   Oct 1997   [Refereed]
Kaneko H, Inoue R, Fukao T, Kasahara K, Tashita H, Teramoto T, Kondo N
Leukemia & lymphoma   27(5-6) 539-542   1996   [Refereed]
Kaneko H, Ariyasu T, Inoue R, Fukao T, Kasahara K, Teramoto T, Matsui E, Hayakawa S, Kondo N
Clin Exp Immunol   111 339-344   1998   [Refereed]
Watanabe H, Yamaguchi S, Kimura M, Wakazono A, Song XQ, Fukao T, Orii T, Hashimoto T
Tohoku J Exp Med   184 29-38   1998   [Refereed]
Molecular basis of selective IgG2 deficiency: The mutated membrane-bound form of gamma2 heavy chain caused complete IgG2 deficiency in two Japanese siblings.
Tashita H, Fukao T, Kaneko H, Teramoto T, Inoue R, Kasahara K, Kondo N
J Clin Invest   101 677-681   1998   [Refereed]
Sewell AC, Herwig J, Wiegratz I, Lehnert W, Niederhoff H, Song XQ, Kondo N, Fukao T
J Inherit Metab Dis   21 441-442   1998   [Refereed]
Perinatal mumps associated with bronchiolitis and respiratory distress.
Fukao T, Hirano A, Nakamura K, Yamazaki Y, Yamada A, Tashita H, Inoue R, Kondo N
Eur J Pediatr   157 952-953   1998   [Refereed]
Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation.
Sukegawa K, Matsuzaki T, Fukuda S, Masuno M, Fukao T, Kokuryu M, Iwata S, Tomatsu S, Orii T, Kondo N
Clin Genet   53 96-101   1998   [Refereed]
Song XQ, Fukao T, Watanabe H, Shintaku H, Hirayama K, Kassovska-Bratinova S,Kondo N, Mitchell GA
Hum Mutat   12 83-88   1998   [Refereed]
Fukao T, Nakamura H, Song XQ, Nakamura K, Orii KE, Kohno Y, Kano M, Yamaguchi S, Hashimoto T, Orii T, Kondo N
Hum Mutat   12 245-254   1998   [Refereed]
Fukao T, Song XQ, Yoshida T, Tashita H, Kaneko H, Teramoto T, Inoue R, Katamura K, Mayumi M, Hiratani M, Taniguchi N, Arai J, Wakiguchi H, Bar-Shira A, Shiloh Y, Kondo N
Hum Mutat   12 338-343   1998   [Refereed]
Kondo N, Kobayashi Y, Shinoda S, Takenaka R, Teramoto T, Kaneko H, Fukao T, Matsui E, Kasahara K, Yokoyama Y
Clin Exp Allergy   28 1340-1344   1998   [Refereed]
Novel exonic mutation (5319 G to A) resulting in two aberrantly spliced transcripts of the ATM gene in a Japanese patient with ataxia-telangiectasia.
Fukao T, Tashita H, Teramoto T, Inoue R, Kaneko H, Komiyama K, Bar-Shira A, Gilad S, Shiloh Y, Nishimura M, Kondo N
Human mutation   Suppl 1 S223-225   1998   [Refereed]
[Mitochondrial acetoacetyl-CoA thiolase deficiency].
Fukao T
Ryoikibetsu shokogun shirizu   (18 Pt 1) 310-313   1998   [Refereed]
[Succinyl-CoA: 3-ketoacid CoA transferase deficiency].
Fukao T
Ryoikibetsu shokogun shirizu   (18 Pt 1) 355-358   1998   [Refereed]
[Cytosolic acetoacetyl-CoA thiolase deficiency].
Song XQ, Fukao T
Ryoikibetsu shokogun shirizu   (18 Pt 1) 359-361   1998   [Refereed]
Teramoto T, Fukao T, Tashita H, Inoue R, Kaneko H, Takemura M, Kondo N
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology   28(1) 74-82   Jan 1998   [Refereed]
Isogai K, Sukegawa K, Tomatsu S, Fukao T, Song XQ, Yamada Y, Fukuda S, Orii T, Kondo N
Journal of inherited metabolic disease   21(1) 60-70   Feb 1998   [Refereed]
DNase I hypersensitive sites in human I epsilon region of immunoglobulin heavy chain genes abnormally induced by interleukin-4 in B-lymphocytes of atopic patients with high levels of serum IgE.
Kondo N, Fukao T, Kaneko H, Teramoto T, Tashita H, Inoue R
Journal of investigational allergology & clinical immunology   8(4) 234-238   Jul 1998   [Refereed]
Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocol.
Yamada Y, Inoue R, Fukao T, Kaneko H, Isogai K, Fukuda S, Shimozawa N, Suzuki Y, Kondo N, Azuma E, Sakurai M
Pediatric hematology and oncology   15(5) 425-429   Sep 1998   [Refereed]
ATM is upregulated during the mitogenic response in peripheral blood mononuclear cells.
Fukao T, Kaneko H, Birrell G, Gatei M, Tashita H, Yoshida T, Cross S, Kedar P, Watters D, Khana KK, Misko I, Kondo N, Lavin MF
Blood   94 1998-2006   1999   [Refereed]
Kaneko H, Matsui E, Fukao T, Kasahara K, Morimoto W, Kondo N
Clin Exp Immunol   118 285-289   1999   [Refereed]
Matsui E, Kaneko H, Fukao T, Teramoto T, Inoue R, Watanabe M, Kasahara K, Kondo N
Biochem Biophys Res Commun   266 551-555   1999   [Refereed]
Time-course study of the levels of urinary leukotriene E4, serum thromboxane B2 and serum eosinophil cationic protein in spontaneous asthma attacks in five children.
Inoue R, Fukao T, Kato Y, Teramoto T, Utsumi M, Kondo N
Journal of investigational allergology & clinical immunology   9(6) 361-366   Nov 1999   [Refereed]
Ueki H, Washino K, Fukao T, Inoue M, Ogawa N, Takai A
Psychiatry and clinical neurosciences   53(6) 621-627   Dec 1999   [Refereed]
[Genetics of neurologic disorders in children].
Kondo N, Suzuki Y, Shimozawa N, Takahashi Y, Fukao T
Nihon rinsho. Japanese journal of clinical medicine   57 Suppl 700-706   Dec 1999   [Refereed]
Characterization of the nuclear localization signal in the DNA helicase responsible for Bloom syndrome.
Hayakawa S, Kaneko H, Fukao T, Kasahara K, Matsumoto T, Furuichi Y, Kondo N
Int J Mol Med   5 477-484   2000   [Refereed]
Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes.
Sukegawa K, Nakamura H, Kato Z, Tomatsu S, Montano AM, Fukao T, Toietta G, Tortora P, Orii T, Kondo N
Hum Mol Genet   9 1283-1290   2000   [Refereed]
Fukao T, Mitchell GA, Song XQ, Nakamura H, Kassovska-Bratinova S, Orii KE, Wraith JE, Besley G, Wanders RJ, Niezen-Koning KE, Berry GT, Palmieri M, Kondo N
Genomics   68 144-151   2000   [Refereed]
Matsui E, Kaneko H, Teramoto T, Fukao T, Inoue R, Kasahara K, Takemura M, Seishima M, Kondo N
Clin Exp Allergy   30 1250-1256   2000   [Refereed]
Kaneko H, Fukao T, Inoue R, Kasahara K, Matsui E, Kondo N
Experimental and clinical immunogenetics   17(4) 173-178   2000   [Refereed]
Immunoblot analysis for laboratory diagnosis of ataxia-telangiectasia: use of Epstein-Barr virus-transformed or phytohemagglutinin-stimulated lymphoblasts for detection of ATM protein.
Fukao T, Yoshida T, Kaneko H, Song XQ, Tashita H, Teramoto T, Inoue R, Watters D, Lavin M, Kondo N
Journal of investigational allergology & clinical immunology   10(1) 36-40   Jan 2000   [Refereed]
Neonatal hypoglycemia in severe succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.
Berry GT, Fukao T, Mitchell GA, Mazur A, Ciafre M, Gibson J, Kondo N, Palmieri MJ
J Inherit Metab Dis   24 587-595   2001   [Refereed]
Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boy.
Doi T, Abo W, Tateno M, Hayashi K, Hori T, Nakada T, Fukao T, Takahashi Y, Terada N
Eur J Pediatr   159 908-911   2001   [Refereed]
Lysinuric Protein Intolerance in Siblings: complication of SLE in the elder sister.
Aoki M, Fukao T, Fujita Y, Watanabe M, Teramoto T, Kato Y, Suzuki Y, Kondo N
Eur J Pediatr   160 522-523   2001   [Refereed]
Myopathic form of very-long chain acyl-CoA dehydrogenase deficiency: evidence for temperature-sensitive mild mutations in both mutant alleles in a Japanese girl.
Fukao T, Watanabe H, Orii K, Takahashi Y, Hirano A, Kondo T, Yamaguchi S, Aoyama T, Kondo N
Pediatr Res   49 227-231   2001   [Refereed]
Nakamura K, Fukao T, Perez-Cerda C, Luque C, Song XQ, Naiki Y, Kohno Y, Ugarte M, Kondo N
Mol Genet Metab   72 115-121   2001   [Refereed]
Yamaguchi S, Iga M, Kimura M, Suzuki Y, Shimozawa N, Fukao T, Kondo N, Tazawa Y, Orii T
J Chromatogr B Biomed Sci Appl   758 81-86   2001   [Refereed]
Gueven N, Keating KE, Chen P, Fukao T, Khanna KK, Watters D, Rodemann PH, Lavin MF
J Biol Chem   276 8884-8891   2001   [Refereed]
Kondo N, Matsui E, Kaneko H, Fukao T, Teramoto T, Inoue R, Watanabe M, Kasahara K, Morimoto N
International archives of allergy and immunology   124(1-3) 117-120   Jan 2001   [Refereed]
Terada T, Kaneko H, Fukao T, Tashita H, Li AL, Takemura M, Kondo N
International immunology   13(2) 249-256   Feb 2001   [Refereed]
Kondo N, Matsui E, Kaneko H, Fukao T, Teramoto T, Inoue R, Watanabe M, Aoki M, Kasahara K, Morimoto N
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology   31(8) 1189-1193   Aug 2001   [Refereed]
Kaneko H, Morimoto W, Fukao T, Kasahara K, Kondo N
Leukemia & lymphoma   42(4) 757-760   Aug 2001   [Refereed]
Purevjav E, Kimura M, Takusa Y, Ohura T, Hara N, Fukao T, Yamaguchi S
Eur J Clin Invest   32 707-712   2002   [Refereed]
Beamish H, Kedar P, Kaneko H, Chen P, Fukao T, Peng C, Beresten S, Gueven N, Purdie D, Lees-Miller S, Ellis N, Kondo N, Lavin MF
J Biol Chem   277 30515-30523   2002   [Refereed]
Takusa Y, Fukao T, Kimura M, Uchiyama A, Doi T, Abo W, Tsuboi Y, Hirose S, Fujioka H, Kishimoto T, Kondo N, Yamaguchi S
Mol Genet Metab   75 227-234   2002   [Refereed]
Fukao T, Nakamura H, Nakamura K, Perez-Cerda C, Baldellou A, Barrionuevo CR, Castello FG, Kohno Y, Ugarte M, Kondo M
Mol Genet Metab   75 235-243   2002   [Refereed]
[3-ketoacyl-CoA thiolase deficiency].
Fukao T, Yamaguchi S
Nihon rinsho. Japanese journal of clinical medicine   60 Suppl 4 738-742   Apr 2002   [Refereed]
Itoh S, Kariya M, Nagano K, Yokoyama S, Fukao T, Yamazaki Y, Mori H
Biological & pharmaceutical bulletin   25(8) 986-990   Aug 2002   [Refereed]

Misc

 
Molecular basis of 3-ketothiolase deficiency.
Fukao T, Yamaguchi S, Kano M, Orii T, Osumi T, Hashimoto T
Prog Clin Biol Res   375 573-581   1992
Molecular basis of 3-ketothiolase deficiency: detection of gene mutation and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolase.
Fukao T, Yamaguchi S, Wakazono A, Okamoto H, Orii T, Osumi T, Hashimoto T
J Inherit Metab Dis   15 815-820   1992
3-ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNA.
Yamaguchi S, Fukao T, Nagasawa H, Orii T, Sakura N, Schutgens R B H, Sweetman L, Fujiki Y, Kamijo K, Osumi T, Hashimoto T
Prog Clin Biol Res   321 673-679   1990
Molecular cloning of cDNA for human mitochondrial acetoacetyl-CoA thiolase and molecular analysis of 3-ketothiolase deficiency.
Fukao T, Yamaguchi S, Nagasawa N, Kano M, Orii T, Fujiki Y, Osumi T, Hashimoto T
J Inherit Metab Dis   13 757-760   1990

Books etc

 
Molecular basis of 3-Ketothiolase deficiency(共著)
New developments in fatty acid oxidation Wiley-Liss, New York   1992   
3-Ketothiolase deficiency : mdecular heterogeneity of the enzyme defect and cloning of the cDNA 共著
Fatty Acid Oxidation : Clinical, Biochemical, and molecular Aspects. Alan. R. Liss inc. New York   1990   
Mitchell GA, Fukao T. Chapter 102 inborn errors of ketone body catabolism.In Molecular and Metabolic Bases of Inherited Disease (8th edition)(Scriver CR,Beaudet AL, Sly WS, Valle Deds)
New York McGraw-Hill, Inc   2001   
Fukao T. Acetoacetyl-CoA thiolase (cytosolic)in Wiley Encyclopedia of Molecular Medicine.
John Wiley & Sons, Inc   2002   
Fukao T. Acetoacetyl-CoA thiolase (Mitochondrial)in Wiley Encyclopedia of Molecular Medicine.
John Wiley & Sons, Inc   2002   

Conference Activities & Talks

 
A common mutation R208X identified in Vietnamese patients with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.
Fukao T, Nguyen TH, Nguyen NT, Can TBN, Vu CD, Pham TVA, Nguyen NK, Kobayashi H, Hasegawa Y, Bui PT, Nguyen TL, Yamaguchi S, Kondo N.
The 1st Asian Congress fro Inherited Metabolic Diseases   2010   
An exonic splicing mutation identified in a beta-ketothiolase-deficient patient.
Fukao T, Naiki Y, Tanaka, Kondo N.
11th International Congress of Inborn Errors of Metabolism   2009   
Clinical and Molecular Aspects of VLCAD Deficiency and Glutaric acidemia Type II in Japanese
Yamaguchi S(pediatrics),Hasegawa Y(pediatrics),Kobayashi H(pediatrics),Yotsumoto Y(pediatrics),Kimura M(pediatrics),Fukao T(pediatrics),Shigematsu Y(pediatrics)
Sep 2005   
Clinical and molecular aspects of VLCAD deficiencyin Japan
Fukao T(pediatrics),Hasegawa Y(pediatrics),Ohashi Y(pediatrics),Nishino I(pediatrics),Shigematsu Y(pediatrics),Kondo N(pediatrics),Yamaguchi S(pediatrics)
Jun 2005   
Clinical and molecular investigations of 5 Japanese patients with mitochondrial trifunctional protein deficiency.
Purevsuren J, Fukao T, Hasegawa Y, Kobayashi H, Fukuda S, Yamaguchi S.
2009   

Research Grants & Projects

 
Clinical and molecular analyses of allergy
Project Year: 1996   
Study on primary immunodeficiency syndromes.
Grant-in-Aid for Scientific Research
Project Year: 1994   
Molecular study of disorders in mitochondrial β-oxidation
Grant-in-Aid for Scientific Research
Project Year: 1994   
Study on the molecular basis of β-Ketothiolase deficiency and succinyl-CoA : 3-ketoacid CoA transferase deficiency.
Grant-in-Aid for Scientific Research
Project Year: 1986