Publications 2000

  • Adachi M, Tachibana K, Asakura Y, Muroya K, Ogata T: Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features. Hum Genet (2000) 106:306-310
  • Araki Y, Hataya H, Tanaka Y, Fukuzawa R, Ikeda M, Kawamura K, Honda M: Long-term peritoneal dialysis is a risk factor of sclerosing encapsulating peritonitis for children. Perit Dial Int (2000) 20:445-451
  • Awazu M, Matsuoka S, Kamimaki T, Watanabe H, Matsuo N: Absent circadian variation of blood pressure in patients with anorexia nervosa. J Pediatr (2000) 136:524-527
  • Bose H, Sato S, Aisenberg J, Shalev S, Matsuo N, Miller W.: Mutations in the steroidogenic acute regulatory protein (StAR) in six patients with congenital lipoid adrenal hyperplasia. J Clin Endocrinol Metab (2000) 85:3636-3639
  • Campana D, Suzuki T, Todisco E, Kitanaka A: CD38 in hematopoiesis. Chem Immunol (2000) 75:169-188
  • Caviness VS Jr, Takahashi T, Nowakowski RS: Neocortical malformation as consequence of nonadaptive regulation of neuronogenetic sequence. Ment Retard Dev Disabil Res Rev (2000) 6:22-33
  • Caviness VS Jr, Takahashi T, Nowakowski RS: Neuronogenesis and the early events of neocortical histogenesis. Results Probl Cell Differ (2000) 30:107-143
  • Fujieda M, Kinoshita A, Naruse K, Nakayama T, Moriki T, Wakiguchi H, Kurashige T: Mumps associated with immunoglobulin A nephropathy. Pediatr Infect Dis J (2000) 19:669-671
  • Fukami M, Kirsch S, Schiller S, Richter A, Benes V, Franco B, Muroya K, Rao E, Merker S, Niesler B, Ballabio A, Ansorge W, Ogata T, Rappold GA: A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation. Am J Hum Genet (2000) 67:563-573
  • Fukushima S, Yamada T, Hashiguchi A, Nakata Y, Hata J.: Augmentation of human leukemic cell invasion by the activation of small GTP-binding protein Rho . Exp Hematol (2000) 28:391-400
  • Goda N, Tanoue A, Kikuchi S, Tsujimoto G: Cloning and characterization of the promotor of murine cytohesin-1 gene. Biochim Biophys Acta (2000) 1493:195-199
  • Gohlke BC , Haug K, Fukami M, Friedl W, Noeker M, Rappold GA , Haverkamp F: Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. J Med Genet (2000) 37:600-602
  • Hanabusa H, Kuji N, Kato S, Tagami H, Kaneko S, Tanaka H, Yoshimura Y.: An evaluation of semen processing methods for eliminating HIV-1. AIDS (2000) 14:1611-1616
  • Hasegawa T, Zhao L, Caron KM, Majdic G, Suzuki T, Shizawa S, Sasano H, Parker KL: Developmental roles of the steroidogenic acute regulatory protein (StAR) as revealed by StAR knockout mice. Mol Endocrinol (2000) 14:1462-1471
  • Hasegawa Y, Fujii K, Yamada M, Igarashi Y, Tachibana K, Tanaka T, Onigata K, Nishi Y, Kato S, Hasegawa T: Identification of novel human GH-1 gene polymorphisms that are associated with growth hormone secretion and height. J Clin Endocrinol Metab (2000) 85:1290-1295
  • Hayashida S, Harrod KS , Whitsett JA.: Regulation and function of CCSP during pulmonary Pseudomonas aeruginosa infection in vivo. Am J Physiol (2000) 279: L452-459
  • He L, Terunuma H, Hanabusa H, Iwamoto A, Oka S, Tanabe F, Chiba N, Kurimoto M, Ikeda M, Okamura H, Dai J, Iwatani Y, Ishida T, Ito M.: Interleukin 18 and interleukin 1beta production is decreased in HIV type 1-seropositive hemophiliacs but not in HIV type 1-seropositive nonhemophiliacs. AIDS Res Hum Retroviruses (2000) 16:345-53
  • Hida M, Shimamura Y, Ueno E, Watanabe J: Childhood idiopathic thrombocytopenic purpura associated with human parvovirus B19 infection. Pediatr Int (2000) 42:708-710
  • Hirai K, Seki T: Cerebrospinal fluid somatostatin levels in febrile seizures and epilepsy in children. Neuropeptides (2000) 34:18-24
  • Ho C, Zhou J, Medina M, Goto T, Jacobson M, Bhide PG, Kosik, KS.: Beta-catenin is a nervous system specific adherens junction protein which undergoes dynamic relocalization during development. J Comp Neurol (2000) 420:261-276
  • Horikoshi Y, Mimaya J, Amano K, Kawano Y, Watanabe A, Watanabe T, Sekine I, Nishikawa K, Tsunematsu Y, Endo M, Eguchi H, Koyama T, Kawakami K, Oka T, Matsushita T, Koizumi S, Fujimoto T, Takaue Y: Feasibility study of autologous peripheral blood stem cell transplantation for the treatment of childhood acute myelogenous leukemia. Jpn J Clin Oncol (2000) 30:137-145
  • Hoshii S, Honda M, Itami N, Oh S, Matsumura C, Moriya S, Mori M, Hatae K, Ito Y, Karashima S.: Sclerosing encapsulating peritonitis in pediatric peritoneal dialysis patients Pediatr Nephrol (2000) 14:275-279
  • Igarashi T, Goto K, Tahara H, Uchimoto S, Omichi K, Kanno H, Hayasaka K, Murase T.: Hetrogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan . Hum Genet (2000) 106:108-115
  • Ikeda K, Hokuto I, Mori K, Hayashida S, Tokieda K, Tanigaki S, Tanaka M, Yuasa Y: Intrauterine MRI with single-shot fast-spin echo imaging showed different signal intensities in hypoplastic lungs. J Perinat Med (2000) 28:151-154
  • Ikeda M, Hamasaki Y, Hataya H, Honda M, Sugai K.: Multiorgan failure induced by intravenous immunoglobulin. Acta Paediatrica (2000) 89: 1393
  • Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y: Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata. Am J Med Genet (2000) 94:300-305
  • Imashuku S, Hibi S, Sako M, Lim Y, Ikuta K, Nakata Y, Mori T, Lizuka S, Horibe K, Tsunematsu Y.: Hemophagocytosis by leukemic blasts in 7 Acute Myeloid Leukemia cases with t(16;21)(p11;q22). Cancer (2000) 88: 1970-1975
  • Ishii T, Ogata T, Sasaki G, Sato S, Kinoshita E, Matsuo N: Novel mutations of the ACTH receptor gene in a female adult patient with adrenal unresponsiveness to ACTH. Clin Endocrinol (Oxf) (2000) 53:389-392
  • Ishii T, Suzuki Y, Ando N, Matsuo N, Ogata T: Novel mutations of the autoimmune regulator gene in two siblings with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. J Clin Endocrinol Metab (2000) 85:2922-2926
  • Ito S, Ikeda M, Asanuma H, Shishido S, Nakai H, Honda M.: A giant urinoma in a neonate without obstructive uropathy Pediatr Nephrol (2000) 14: 831-832
  • Kakinuma Y, Miyauchi T, Yuki K, Murakoshi N, Yamaguchi I, Goto K.: Mitochondrial dysfunction of cardiomyocytes causing an impairment of cellular energy metabolism induces apoptosis, which is accompanied by an increase in cardiac ET-1 expression J Cardiovasc Pharmacol (2000) 36:S201-204
  • Kaneko A, Miyazawa H, Kirikae F, Hashimoto M, Toyooka K, Kuratsuji T et al: Epidemiological analysis of a methicillin-resistant staphylococcus aureus outbreak in a neonatal intensive care unit after cleaning of envirinmental surfaces in the unit by genomic DNA finger printing using pulsed-field gel electrophoresis. Jpn J Infect Dis (2000) 53:130-131
  • Kaneko M, Watanabe J, Nakano N, Ueno E: Campylobacter jejuni bacteremia in an immunocompetent Japanese child. Pediatr Int (2000) 42:579-581
  • Kikuchi S, Tanoue A, Endo F, Wakasugi S, Matsuo N, Tsujimoto G: A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiency. J Hum Genet (2000) 45:102-104
  • Kirsch S, Wei B, De Ross M, Ogata T, Lombardi G, Rappold GA. : FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY. J Med Genet (2000) 37:593-599
  • Kobayashi Y, Honda M, Yoshikawa N, Ito H: Acute tubulointerstitial nephritis in 21 Japanese children. Clin Nephrol (2000) 54:191-197
  • Kosaki K, Kosaki R, Craigen WJ, Matsuo N: Isoform-specific imprinting of the human PEG1/MEST gene. Am J Hum Genet (2000) 66:309-312
  • Kosaki K, Kosaki R, Robinson WP, Craigen WJ, Shaffer LG, Sato S, Matsuo N: Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assay. J Med Genet (2000) 37:E19
  • Kosho T, Nakamura T, Kaneko T, Tamura M.: A Case of neonatal-onset carbamoyl-phosphate synthase I deficiency treated by continuous hemodiafiltration. E J Pediatr (2000) 159: 629-630
  • Kosuga M, Enosawa S, Li XK, Suzuki S, Matsuo N, Yamada M, Roy Chowdhury J, Koiwai O, Okuyama T: Strong, long-term transgene expression in rat liver using chicken beta-actin promoter associated with cytomegalovirus immediate-early enhancer (CAG promoter). Cell Transplant (2000) 9:675-680
  • Kosuga M, Takahashi S, Sasaki K, Enosawa S, Li XK, Okuyama S, Fujino M, Suzuki S, Yamada M, Matsuo N, Sakuragawa N, Okuyama T: Phenotype correction in murine mucopolysaccharidosis type VII by transplantation of human amniotic epithelial cells after adenovirus-mediated gene transfer. Cell Transplant (2000) 9:687-692
  • Kosuga M, Takahashi S, Sasaki K, Li XK, Fujino M, Hamada H, Suzuki S, Yamada M, Matsuo N, Okuyama T: Adenovirus-mediated gene therapy for mucopolysaccharidosis VII: involvement of cross-correction in wide-spread distribution of the gene products and long-term effects of CTLA-4Ig coexpression. Mol Ther (2000) 1:406-413
  • Kumagai T, Nakayama T, Kamada M, Igarashi C, Yuri K, Furukawa H, Wagatuma K, Tsutsumi H, Chiba S, Kojima H: The lymphoproliferative response to enzymatically digested gelatin in subjects with gelatin hypersensitivity. Clin Exp Allergy (2000) 30: 1430-1435
  • Kwada A, Kashima A, Shiraishi H, Gomi H, Matsuo I, Yasuda K, Sasaki G, Sato S, Orimo H.: Pyridoxine-induced photosensitivity and hypophosphatasia. Dermatol (2000) 201:356-360
  • Li XK, Fujino M, Guo L, Okuyama T, Funeshima N, Hashimoto M, Okabe K, Yaginuma H, Mikoshiba K, Enosawa S, Amemiya H, Suzuki S.: Inhibition of Fas-mediated fulminant hepatitis in CrmA gene-transfected mice. Biochem Biophys Res Commun (2000) 273:101-109
  • Lichtner P, Konig R, Hasegawa T, Esch HV, Meitinger T, Schuffenhauer S.: An HDR(hypoparathyroidism, deafness, renal defect) syndrome locus maps distal to the DiGeorge syndrome regions on 10p13/14. J Med Genet (2000) 37:33-37
  • Maeda J, Yamagishi H, Matsuoka R, Ishihara J, Tokumura M, Fukushima H, Ueda H, Takahashi E, Yoshiba S, Kojima Y: Frequent association of 22q11.2 deletion with tetralogy of Fallot. Am J Med Genet (2000) 92:269-272
  • Matsuo M, Muroya K, Adachi M, Tachibana K, Asakura Y, Nakagomi Y, Hanaki K, Yokoya S, Yoshizawa A, Igarashi Y, Hanew K, Matsuo N, Ogata T: Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development. Hum Genet (2000) 107:433-439
  • Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T: Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns. Am J Med Genet (2000) 91:267-272
  • Matsuo N: Recently identified growth gene, SHOX Intern Med News (2000) 382:4-5
  • Matsuo N, Anzo M, Sato S, Ogata T, Kamimaki T.: Testicular volume in Japanese boys up to the age of 15 years. Eur J Pediatr (2000) 159: 843-845
  • Miura H, Morikawa Y, Ueda H.: Hyperpolarization is not responsible for the acetylcholine induced negative chronotropic action in the presence of isoproterenol, Bas Res Cardiol (2000) 95:442-448
  • Miura T, Kimura K: Theophylline-Induced Convulsions in Children with Epilepsy. Pediatrics (2000) 105:920
  • Miyama S, Arimoto K, Kimiya S, Tomi H.: Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation. Neuropediatrics (2000) 31: 214-217
  • Miyamoto J, Koto S, Hasegawa Y: Final height of Japanese patients with X-linked hypophosphatemic rickets: effect of vitamin D and phosphate therapy. Endocr J (2000) 47:163-167
  • Mori T, Kiyokawa N, Katagiri UY, Taguchi T, Suzuki T, Sekino T, Sato N, Ohmi K, Nakajima H, Takeda T, Fujimoto J.: Globotriaosyl ceramide (CD77/Gb3) in the glycolipid-enriched membrane domain participates in the B cell receptor-mediated apoptosis by regulating Lyn kinase activity in human B cells. Exp Hemat (2000) 28:1260-1268
  • Morikawa Y, Ohashi Y, Harada K, Asai T, Okawa S, Nagashima M, Katoh T, Baba K, Furusho K, Okuni M, Osano M.: Coronary Risks after high-dose Gamma Globulin in Children with Kawasaki Disease. Pediatr Int (2000) 42:464-469
  • Murakoshi N, Kakinuma Y, Miyauchi T, Yuki K, Yamaguchi I.: Impairment of cardiac energy metabolism in vivo causes hemodynamic abnormality and upregulation of myocardial preproendothelin-1 mRNA. J Cardiovasc Pharmacol (2000) 36:S128-131
  • Murakoshi N, Miyauchi T, Kakinuma Y, Yuki K, Goto K, Yanagisawa M, Yamaguchi I. : Vascular remodeling after vascular injury of the carotid artery is enhanced in endothelin-B receptor-deficient mice. Circulation (2000) 102:I-825
  • Muroya K, Okuyama T, Goishi K, Ogiso Y, Fukuda S, Kameyama J, Sato H, Suzuki Y, Terasaki H, Gomyo H, Wakui K, Fukushima Y, Ogata T: Sex-determining gene(s) on distal 9p: clinical and molecular studies in six cases. J Clin Endocrinol Metab (2000) 85:3094-3100
  • Nagai T, Matsuo N, Kayanuma Y, Tonoki H, Fukushima Y, Ohashi H, Murai T, Hasegawa T, Kuroki Y, Niikawa N: Standard growth curves for Japanese patients with Prader-Willi syndrome. Am J Med Genet (2000) 95:130-134
  • Nakajima-Nakano K, Makioka A, Yamashita N, Matsuo N, Asai T: Evaluation of serodiagnosis of toxoplasmosis by using the recombinant nucleoside triphosphate hydrolase isoforms expressed in Escherichia coli. Parasitol Int (2000) 48:215-222
  • Nakao A, Imai S, Takano T: Transposon-mediated insertional mutagenesis of the D-alanyl-lipoteichoic acid (dlt) operon raises methicillin resistance in Staphylococcus aureus. Res Microbiol (2000) 151:823-829
  • Nakayama T, Aizawa C: Change in gelatin content of vaccines associated with reduction in reports of allergic reactions. J Allergy Clin Immunol (2000) 106:591-592
  • Nanao K, Hasegawa Y.: Polymorphisms at the 5′ end of the human gonadotropin-releasing hormone receptor gene are not associated with timing of menarche in Japanese girls. Eur J Endocrinol (2000) 143:555-556
  • Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N: Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature. J Clin Endocrinol Metab (2000) 85:2927-2930
  • Ogata T, Matsuo N, Hiraoka N, Hata J.: X-linked lissencephaly with ambiguous genitalia: delineation of further case. Am J Med Genet (2000) 94:174-176
  • Ogata T, Muroya K, Sasagawa I, Kosho T, Wakui K, Sakazume S, Ito K, Matsuo N, Ohashi H, Nagai T.: Genetic evidence for a novel gene(s) involved in urogenital development on 10q26. Kidney Int (2000) 58: 2281-2290
  • Ogata T, Wakui K, Kosho T, Muroya K, Yamanouchi Y, Takano T, Fukushima Y, Rappold G, Suzuki Y: Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation. Am J Med Genet (2000) 92:256-259
  • Okubo M, Horinishim A, Takeuchim M, Suzuki Y, Sakura N, Hasegawa Y, Igarashi T, Goto K, Tahara H, Uchimoto S, Omichi K, Kanno H, Hayasaka K, Murase T.: Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan . Hum Genet (2000) 106:108-115
  • Okubo M, Horinishim A, Takeuchim M, Suzuki Y, Sakura N, Hasegawa Y, Igarashi T, Goto K, Tahara H, Uchimoto S, Omichi K, Kanno H, Hayasaka K, Murase T.: Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan . Hum Genet (2000) 106:108-115
  • Omori S, Hida M, Ishikura K, Kuramochi S, Awazu M: Expression of mitogen-activated protein kinase family in rat renal development. Kidney Int (2000) 58:27-37
  • Sakuragawa N, Enosawa S, Ishii T, Thangavel R, Tashiro T, Okuyama T, Suzuki S: Human amniotic epithelial cells are promising transgene carriers for aoogeneic cell transplantation into liver. J Hum Genet (2000) 45:171-176
  • Sasagawa I, Suzuki Y, Tateno T, Nakada T, Muroya K, Ogata T: CAG repeat length of the androgen receptor gene in Japanese males with cryptorchidism. Mol Hum Reprod (2000) 6:973-975
  • Sato N, Kiyokawa N, Taguchi T, Suzuki T, Sekino T, Ohmi K, Itagaki M, Sato T, Lepage A, Lanza F, Fujimoto J: Functional conservation of platelet glycoprotein V promoter between mouse and human megakaryocytes. Exp Hematol (2000) 28:802-814
  • Sato N, Kiyokawa N, Takada K, Itagaki M, Saito M, Sekino M, Suzuki T, Taguchi T, Mimori K, Lanza F, Fujimoto J: Characterization of monoclonal antibodies against mouse and rat platelet glycoprotein V (CD42d). Hybridoma (2000) 19:455-461
  • Schiller S, Spranger S, Schechinger B, Fukami M, Merker S, Drop SLS, Troeger J, Knoblauch H, Kunze J Seidel J, Rappold GA.: Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome. Eur J Hum Genet (2000) 8:54-62
  • Serizawa I, Amano K, Ishii H, Ichikawa T, Kusaka M, Taguchi T, Kiyokawa N, Fujimoto J: Long-term overexpression of human granulocyte colony-stimulating factor in transgenic mice: persistent neutrophilia with no increase mortality for more than one year. Cytokine (2000) 12:630-635
  • Shen L, Miyauchi J, Kato J, Honna T, Tsunematsu Y, Tsuchida R, Kato J, Mizutani S: Differentiation-associated expression and intracellular localization of cydin-dependent kinase inhibitor p27KIP1 and c-Jun co-activator JAB1 in neuroblastoma. Int J Oncol (2000) 17:749-754
  • Shimada H, Arai Y, Sekiguchi S, Ishii T, Tanitsu S, Sasaki M.: Generation of the NUP98-HOXD13 fusion transcript by a rare translocation, t(2;11)(q31;p15), in a case of infant leukaemia. Br J Haematol (2000) 110:210-213
  • Shimada H, Ichikawa H, Nakamura S, Katsu R, Iwasa M, Kitabayashi I, Ohki M.: Analysis of genes under the downstream control of the t(8;21) fusion protein AML1-MTG8: overexpression of the TIS11b(ERF-1, cMG1) gene induces myeloid cell proliferation in response to G-CSF. Blood (2000) 96:655-663
  • Shimizu S, Chen KR, Tagami H, Hanabusa H.: Mucocutaneous manifestations in Japanese HIV-positive hemophiliacs. Dermatology (2000) 201:321-325
  • Shinjoh M, Bamba M, Jozaki K, Takahashi E, Koinuma G, Sugaya N: Influenza A-associated encephalopathy with bilateral thalamic necrosis in Japan. Clin Infect Dis (2000) 31:611-613
  • Shinjoh M, Omoe K, Saito N, Matsuo N, Nerome K: In vitro growth profiles of respiratory syncytial virus in the presence of influenza virus. Acta Virol (2000) 44:91-97
  • Sugaya N: Influenza vaccine, anti-influenza drugs, and rapid diagnosis in Japan . J Infect Chemother (2000) 6:77-80
  • Sugaya N: Influenza-associated encephalopathy in Japan : pathogenesis and treatment. Pediatr Int (2000) 42:215-218
  • Sugaya N, Mitamura K, Nirasawa M, Takahashi K: The impact of winter epidemics of influenza and respiratory syncytial virus on paediatric admissions to an urban general hospital. J Med Virol (2000) 60:102-106
  • Taguchi T, Kiyokawa N, Sato N, Saito M, Fujimoto J: The characteristic expression of Hck in human B cell precursors. Exp Hematol (2000) 28:55-64
  • Takahashi M, Nakayama T, Kashiwagi Y, Takami T, Sonoda S, Yamanaka T, Ochiai H, Ihara T, Tajima T: Single genotype of measles virus is dominant whereas several genotypes of mumps virus are co-circulating. J Med Virol (2000) 62:278-85
  • Takami T, Sonoda S, Houjyo H, Kawashima H, Takei Y, Miyajima T, Takekuma K, Hoshika A, Mori T, Nakayama T: Diagnosis of horizontal enterovirus infections in neonates by nested PCR and direct sequence analysis. J Hospital Infect (2000) 45:283-287
  • Takata A, Kikuchi H, Fukuzawa R, Ito S, Honda M, Hata J.: Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy. J Med Genet (2000) 37:697-701
  • Tamada K, Kohga M, Takeuchi Y, Masuda E, Hattori K, Kim N.: Seroloical silent hepatitis B virus infection in infant. Pediatr Internat (2000) 42:375-379
  • Tateno T, Sasagawa I, Ashida J, Nakada T, Ogata T: Absence of Y chromosome microdeletions involving the DAZ (deleted in azoospermia) and RBM (ribonucleic acid-binding motif) genes in patients with chordee without hypospadias. Arch Androl (2000) 45:9-12
  • Tateno T, Sasagawa I, Ashida J, Nakada T, Ogata T: Absence of Y-chromosome microdeletions in patients with isolated hypospadias. Fertil Steril (2000) 74:399-400
  • Tharavichitkul P, Kirikae F, Kaneko A, Hashimoto M, Toyooka K, Kuratsuji T et al: Comparison of genomic DNA finger printing using pulsed-field gel electrophoresis and antibiotic susceptibility of clinical isolates of methicillin-resistant staphylococcus aureus between Chiang Mai and Tokyo . Jnp J Infect Dis (2000) 53:86-87
  • Todisco E, Suzuki T, Srivannaboon K, Coustan-Smith E, Raimondi SC , Behm FG, Kitanaka A, Campana D.: CD38 ligation inhibits normal and leukemic myelopoiesis. Blood (2000) 95:535-542
  • Todoroki T, Matsumoto K, Watanabe K, Tashiro Y, Shimizu M, Okuyama T, Imai K.: Accumulated lipids, aberrant fatty acid composition and defective cholesterol ester hydrolase activity in cholesterol ester storage. Ann Clin Biochem (2000) 37:187-193
  • Toyoda Y, Manabe A, Tsuchida M, Hanada R, Ikuta K, Okimoto Y, Ohara A, Ohkawa Y, Mori T, Ishimoto K, Sto T, Kaneko T, Maeda M, Koike K, Shitara T, Hoshi Y, Hosoya R, Tsunematsu Y, Bessho F, Nakazawa S, Saito T.: Six months of maintenance chemotherapy after intensified treatment for acute lymphoblastic leukemia of childhood. J Clin Oncol (2000) 18:1508-1516
  • Tsuchida M, Ikuta K, Hanada, R, Saito T, Isoyama K, Sugita K, Toyoda Y, Manabe A, Koike K, Kinoshita A, Maeda M, Ishimoto K, Sato T, Okimoto Y, Kanekko T, Kajiwara M, M, Sotomatsu Hayashi Y, Yabe H, Hosoya R, Hoshi Y, Ohira M, Bessho F, Tsunemastu Y, Tsukimoto I, Nakazawa S, for the Tokyo Children’s Cancer Study Group.: Long-term follow-up of childfood acute lymphoblastic leukemia in Tokyo Children’s Cancer Study Group 1981-1995. Leukemia (2000) 14:2295-2306
  • Verney C, Takahashi T, Bhide PG, Nowakowski RS, Caviness VS Jr: Independent controls for neocortical neuron production and histogenetic cell death. Dev Neurosci (2000) 22:125-138
  • Verrina E, Honda M, Warady BA, Piraino B.: Prevention of peritonitis in children on peritoneal dialysis Periton Dialysis Int (2000) 20:625-30
  • Warady BA, Schaefer F, Holloway M, Alexander S, Kandert M, Piraino B, Salusky Tranaeus A, Divino J, Honda M, Mujais S, Verrina E.: Consensus guidelines for the treatment of peritonitis in pediatric patients receiving peritoneal dialysis. Perit Dial Int (2000) 20:610-624
  • Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LCP, Eussen BHJ, Van Hemel JO, Lozzio C, Schwartz S, Dow hanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D.: Molecular cytogenetic analysis of eight inversion duplication of human chromosome 13q that each contain a neocentromere. Am J Human Genet (2000) 66:1794-1806
  • Watanabe H: Mental health from infancy onward. Asian Med J (2000) 43:398-404
  • Yamagishi H, Maeda J, Tokumura M, Yoshiba S, Takahashi E, Fukushima H, Yamagishi C, Matsuo N, Kojima Y: Ventricular septal defect associated with microdeletions of chromosome 22q11.2. Clin Genet (2000) 58:493-496
  • Yamagishi H, Olson EN, Srivastava D: The basic helix-loop-helix transcription factor, dHAND, is required for vascular development. J Clin Invest (2000) 105:261-270
  • Yamanaka H, Yamanaka J, Okazaki K, Hayakawa E, Miyazawa H, Kuratsuji T et al: Cytomegalovirus infection of newborns infected with HIV-1 from mother: Case Report. Jpn J Infect Dis (2000) 53:215-216
  • Yanai K, Saito T, Kakinuma Y, Kon T, Hirota K, Taniguchi-Yanai K, Nishijo N, Shigematsu Y, Horiguchi H, Kasuya Y, Sugiyama F, Yagami K, Murakami K, Fukamizu A.: Renin-dependent cardiovascular functions and renin-independent blood-brain barrier functions revealed by renin-deficinet mice. J Biol Chem (2000) 275:5-8
  • Yoshihashi H, Maeyama K, Kosaki R, Ogata T, Tsukahara M, Goto Y, Hata J, Matsuo N, Smith RJ, Kosaki K: Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome. Am J Hum Genet (2000) 67:476-482
  • Yuki K, Miyauchi T, Kakinuma Y, Murakoshi N, Hayashi J, Goto K, Yamaguchi I. : Mitochondrial dysfunction increases expression of endothelin-1 and followed by induction of apoptosis through caspase-3 activation in rat cardiomyocytes in vitro. J Cardiovasc Pharmacol (2000) 36:S205-208