-
Kato Z, Watanabe M, Kondo N：IgG 2, IgG 4 and IgA deficiency possibly associated with carbamazepine treatment. Eur J Pediatr 162, 209-211 (2003)
- Tomatsu S, Orii KO, Vogler C, Grubb JH, Snella EM, Gutierrez M, Dieter T,
Holden CC, Sukegawa K, Orii T, Kondo N, Sly WS：Production of MPS VII mouse (Gus (tm (hE 540A. mE 536A) Sly)) doubly tolerant to human and mouse beta-
glucuronidase. Hum Mol Genet 12, 961-973 (2003)
- Shimozawa N, Nagase T, Takemoto Y, Ohura T, Suzuki Y, Kondo N：Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients：Evidence for a founder haplotype for the most common PEX 10 gene mutation. Am J Med Genet 120A, 40-43 (2003)
- Aoki M, Matsui E, Kaneko H, Inoue R, Fukao T, Watanabe M, Teramoto T,
Kato Z, Suzuki K, Suzuki Y, Kasahara K, Kondo N：A novel single-nucleotide
substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases. Int J Mol Med 12, 185-191 (2003)
- Ito R, Ozaki YA. Yoshikawa T, Hasegawa H, Sato Y, Suzuki Y, Inoue R, Morishima T, Kondo N, Sata T, Kurata T, Tamura S：Roles of anti-hemagglutinin IgA and IgG antibodies in different sites of the respiratory tract of vaccinated mice in preventing lethal influenza pneumonia. Vaccine 21, 2362-2371 (2003)
- Montano AM, Kaitila I, Sukegawa K, Tomatsu S, Kato Z, Nakamura H, Fukuda S, Orii T, Kondo N : Mucopolysaccharidosis IVA : characterization of a common mutationfound in Finnish patients with attenuated phenotype. Hum Genet 113, 162-169 (2003)
- Higa S, Hirano T, Mayumi M, Hiraoka M, Ohshima Y, Nambu M, Yamaguchi E, Hizawa N, Kondo N, Matsui E, Katada Y, Miyatake A, Kawase I, Tanaka T：
Association between interleukin-18 gene polymorphism 105A／C and asthma. Clin Exp Allergy 33, 1097-1102 (2003)
- Ohnishi H, Kato Z, Watanabe M, Fukutomi O, Ito R, Teramoto T, Kondo N：Interleukin-18 is associated with the severity of atopic dermatitis. Allergol Int 52, 123-130 (2003)
- Kasahara Y, Kaneko H, Fukao T, Terada T, Asano T, Kasahara K, Kondo N：Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminase. J Allergy Clin Immunol 112, 755-760 (2003)
- Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y：Mutations in novel peroxin gene PEX 26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J Hum Genet 73, 233-246 (2003)
- Kato Z, Kozawa R, Hashimoto K, Kondo N：Transient lesion in the splenium of the corpus callosum in acute cerebellitis. J Child Neurol 18, 291-292 (2003)
- Kato Z, Jee J, Shikano H, Mishima M, Ohki I, Ohnishi H, Li A, Hashimoto K, Matsukuma E, Omoya K, Yamamoto Y, Yoneda T, Hara T, Kondo N, Shirakawa M：Structure of interleukin-18 and the binding mode. Nature Struct Biol 10, 966-971
(2003)
- Gueven N, Keating K, Fukao T, Loeffler H, Kondo N, Rodemann HP, Lavin MF：Site-directed mutagenesis of the ATM promoter：consequences for response to
proliferation and ionizing radiation. Genes Chromosomes Cancer 38, 157-167 (2003)
- Teramoto T, Kaneko H, Funato M, Sawa H, Nagashima K, Hirose Y, Kondo N：Progressive multifocal leukoencephalopathy in a patient with X-linked agamma-globulinemia. Scand J Infect Dis 35, 909-910 (2003)
- Terada T, Kaneko H, Fukao T, Teramoto T, Asano T, Li AL, Kasahara K, Kondo N :Semiquantitative evaluation of mRNAs for the membranous form of immunoglobulin heavy chain is useful for investigating the etiology in CVID. Scand J Immunol 58, 649-654 (2003)
- Inoue R, Teramoto T, Nakade S, Okamoto H, Yukawa E, Higuchi S, Kondo N, Mikawa H：Population pharmacokinetics of pranlukast hydrate dry syrip in children with bronchial asthma. Allergol Int 52, 213-218 (2003)
- Takahashi Y, Mori H, Mishina M, Watanabe M, Fujiwara T, Shimomura J, Aiba H, Miyajima T, Saito Y, Nezu A, Nishida H, Imai K, Sakaguchi N, Kondo N：
Autoantibodies to NMDA receptor in patients with chronic forms of epilepsia
partialis continua. Neurology 61, 891-896 (2003)
- Li A, Kato Z, Ohnishi H, Hashimoto K, Matsukuma E, Omoya K, Yamamoto Y, Kondo N：Optimized gene synthesis and high expression of human interleukin-18. Protein Exp Purif 32, 110-118 (2003)
- Kurotaki N, Harada N, Shimokawa O, Miyake N, Kawame H, Uetake K, Makita Y, Kondoh T, Ogata T, Hasegawa T, Nagai T, Ozaki T, Touyama M, Shenhav R, Ohashi H, Medne L, Shiihara T, Ohtsu S, Kato Z, Okamoto N, Nishimoto J, Lev D, Miyoshi Y, Ishikiriyama S, Sonoda T, Sakazume S, Fukushima Y, Kurosawa K, Cheng JF, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N：Fifty microdeletions among 112 cases of Sotos syndrome：low copy repeats possibly mediate the common deletion. Hum Mutat 22：378-387 (2003)
- Tomoda A, Nomura K, Shiraishi S, Hamada A, Ohmura T, Hosoya M, Miike T, Sawaishi Y, Kimura H, Takashima H, Tohda Y, Mori K, Kato Z, Fukushima A,
Nishio H, Nezu A, Nihei K：Trial of intraventricular ribavirin therapy for subacute sclerosing panencephalitis in Japan. Brain Dev 25：514-517 (2003)
- Kato Z, Kozawa R, Teramoto T, Hashimoto K, Shinoda S, Kondo N：Acute
cerebellitis in primary human herpesvirus-6 infection. Eur J Pediatr 162：801-803
(2003)
- Takemoto Y, Suzuki Y, Horibe R, Shimozawa N, Wanders RJA, Kondo N：Gas Chromatography ／ Mass Spectrometry Analysis of Very Long Chain Fatty Acids, Docosahexaenoic acid, Phytanic Acid and Plasmalogen for the Screening of
Peroxisomal Disorders. Brain Dev 27, 481-487 (2003)
- Jia Y, Qi C, Zhang Z, Hashimoto T, Rao MS, Huyghe S, Suzuki Y, Van Veldhoven PP, Baes M, and Reddy JK：Overexpression of PPARα (regulated genes in liver in the absence of peroxisome proliferation in mice deficient in both L- and D- forms of enoyl-CoA hydratase／dehydrogenase enzymes of peroxisomal β-oxidation system. J Biol Chem 278, 47232-47239 (2003)
- Une M, Iguchi Y, Sakamoto T, Tomita T, Suzuki Y, Morita M, Imanaka T：ATP-Dependent Transport of Bile Acid Intermediates across Rat Liver Peroxisomal Membranes. J Biochem 134, 225-230 (2003)
- Gootjes J, Elpeleg O, Eyskens F, Mandel H, Mitanchez D, Shimozawa N, Suzuki Y, Waterham HR, Wanders RJ：Novel Mutations in the PEX 2 Gene of Four Unrelated Patients with a Peroxisome Biogenesis Disorder. Pediatr Res 55, 1-6 (2003)
- Fukao T, Matsuo N, Zhang GX, Urasawa R, Kubo T, Kohno Y, Kondo N：Single base substitutions at the initiator codon in the mitochondrial acetoacetyl-CoA thiolase (ACAT 1／T 2) gene result in production of varying amounts of wild-type T 2 polypeptide. Hum Mutat 21, 587-592 (2003)
- Fukao T, Zhang G-X, Sakura N, Kubo T, Yamaga H, Hazama H, Kohno Y, Matsuo N, Kondo M, Yamaguchi S, Shigematsu Y, Kondo N：The mitochondrial acetoacetyl-CoA thiolase deficiency in Japanese patients：urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T 2-deficient patients with some residual T 2 activity. J Inherit Metab Dis 26, 423-431 (2003)
- Shiroma N, Kanazawa N, Kato Z, Shimozawa N, Imamura A, Ito M, Ohtani K, Oka A, Wakabayashi K, Iai M, Sugai K, Sasaki M, Kaga M, Ohta T, Tsujino S：Molecular genetic study in Japanese patients with Alexander disease：a novel muta-tion, R 79L. Brain Dev 25, 116-121 (2003)
- Kikuchi M, Hatano N, Yokota S, Shimozawa N, Imanaka T, Taniguchi H：Proteomic analysis of rat liver peroxisome：Presence of peroxisome-specific isozyme of lon protease. J Biol Chem 279, 421-428 (2004)
- Kondo N, Matsui E, Kaneko H, Aoki M, Kato Z, Fukao T, Kasahara K, Morimoto N：RNA editing of interleukin-12 receptor β2, 2451 C-to-U (Ala 604 Val) conversion, associated with atopy. Clin Exp Allergy 34, 363-368 (2004)
- Shimozawa N, Tsukamoto T, Nagase T, Takemoto Y, Koyama N, Suzuki Y,
Komori M, Ohsumi T, Gootjes J, Ronald JAW, Kondo N：Identification of a New Complermentation Group of the Peroxisome Biogenesis Disorders and PEX 14 as the Mutated Gene. Hum Mutat 23, 552-558 (2004)
- Nagase T, Shimozawa N, Takemoto Y, Suzuki Y, Komori M, Kondo N：
Peroxisomal localization in the developing mouse cerebellum：Implications for
neuronal abnormalities related to deficiencies in peroxisomes. Biochim Biophys Acia 17, 26-33 (2004)
- Tomatsu S, Okamura K, Taketani T, Orii KO, Nishioka T, Gutierrez MA,
Velez-Castrillon S, Fachel AA, Grubb JH, Cooper A, Thornley M, Wraith ED,
Barrera LA, Giugliani R, Schwartz IV, Frenking GS, Beck M, Kircher SG,
Paschke E, Yamaguchi S, Ullrich K, Isogai K, Suzuki Y, Orii T, Kondo N,
Creer M, Noguchi A：Development and testing of new screening method for keratin sulfate in mucopolysaccharidosis IVA. Pediatr Res 55, 592-597 (2004)
- Fukao T, Chen P, Ren J, Kaneko H, Yamamoto K-I, Takeda S, Kondo N, Lavin M： Disruption of the BLM gene in ATM-null DT 40 cells does not exacerbate either
phenotype. Oncogene 23, 1498-1506 (2004)
- Asano T, Kaneko H, Terada T, Kasahara Y, Fukao T, Kasahara K, Kondo N：Molecular analysis of B cell differentiation in selective or partial IgA deficiency. Clin Exp Immunol 136, 284-290 (2004)
- Fukao T, Lopaschuk GD, Mitchell GA：Pathways and control of ketone body metabolism：on the fringe of lipid biochemistry. Prostaglandins, Leukotrienes and Essential Fatty Acids 70：243-251 (2004)
- Fukao T, Matsuo N, Zhang GX, Sakaguchi N, Kohno Y, Kondo N：Mitochondrial Acetoacetyl-CoA Thiolase (T 2, methylaceto-acetyl-CoA thiolase) deficiency：a defect in amino acid and ketone body metabolism. "Symposia Proceedings" of the Pediatric Metabolic Symposium 2002
- Kato Z, Okuda M, Okumura Y, Nishimura M, Kaneko H, Kondo N：Oral administration of the thyrotropin-releasing hormone analogue, taltireline hydrate, in spinal muscular atrophy. J Child Neurol (in press)
- Suzuki Y, Niwa M, Chirasak K, Takahashi Y：A Trial of an International Internet PBL on HIV／AIDS. J Medical Education (in press)
- Suzuki Y, Niwa M, Fujisaki K, Nakamura H, Washino K, Kato T, Ito K, Okano Y, Takahashi Y：Effects of PBL-Tutorial in Gifu University School of Medicine：
Evaluation of Students in Clinical Years. J Medical Education (in press)
- Kondo N, Matsui E, Kaneko H, Kato Z, Teramoto T, Shikano H, Aoki M, Onishi H, Tatebayashi K, Omoya K, Kondo M, Matsukuma E, Kasahara K, Morimoto N：
Genetic defects in downregulation of IgE production and a new genetic classification of atopy. Allergol Int (in press)
- Yoshikawa K, Matsui E, Inoue R, Kaneko H, Teramoto T, Aoki M, Kasahara K, Shinoda S, Fukutomi O, Kondo N：Urinary leukotriene E 4 and 11-dehydro-thromboxane B 2 excretion in children with bronchial asthma. Allergol Int (in press)
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