研究業績

Publications 1996

  • Aoyama T: A cellular pertussis vaccines developed in Japan and their application for disease control J Infect Dis (1996) 174:S264-269
  • Aoyama T, Sunagawa K, Iwata S, Takeuchi Y, Fujii R: Efficacy of short-term treatment of pertussis with clarithromycin and azithromycin J Pediatr (1996) 129:761-764
  • Asayama K, Hayashibe H, Mishiku Y, Honda M, Ito H, Nakazawa S.: Increased activity of plasma cholesterol ester transfer protein in children with end-stage renal disease receiving continuous ambulatory peritoneal dialysis Nephron (1996) 72:231-236
  • Ashizawa K, Asami T, Anzo M, Matsuo N, Matsuoka H, Murata M, Ohtsuki F, Satoh M, Tanaka T, Tatara H, Tsukagoshi K.: Standard RUS skeletal maturation of Tokyo children. Ann Hum Biol (1996) 23:457-69
  • Azuma N, Nishina S, Yanagisawa H, Okuyama T, Yamada M: PAX6 missense mutation in isolated foveal hypoplasia. Nat Genet (1996) 13:141-142
  • Caviness VS Jr, Takahashi T, Miyama S, Nowakowski RS, Delalle I: Regulation of normal proliferation in the developing cerebrum potential actions of trophic factors. Exp Neurol (1996) 137:357-366
  • Coats S, Pledgers W, Awazu M, Daniel T: Detergent solubility defines an alternative itinerary for a subpopulation of PDGF b receptors. J Cell Physiol (1996) 168:412-423
  • Hagiwara T, Inaba H, Yoshida S, Nagaizumi K, Arai M, Hanabusa H, Fukutake K.: A novel mutation Gly 1672-->Arg in type 2A and a homozygous mutation in type 2B von Willebrand disease. Thromb Haemost (1996) 76:253-257
  • Hamvas A, Wise H, Yang RK, Wampler NS, Noguchi A, Maurer MM, Walentik CA, Schramm WF, Cole FS: The influence of the wider surfactant use on neonatal mortality among blacks and whites N Eng J Med (1996) 334:1635-1640
  • Hasegawa T, Hasegawa Y, Aso T, Koto S, Tanaka N, Asamura S, Nagai T, Tsuchiya Y: The transition from latent to overt hypoparathyroidism in a child with CATCH 22 who showed subnormal parathyroid hormone response to ethylenediaminetetraacetic acid infusion. Eur J Pediatr (1996) 155:255
  • Hasegawa T, Hasegawa Y, Aso T, Koto S, Tanaka N, Asamura S, Nagai T, Tsuchiya Y: Transition from latent to overt hypoparathyroidism in a child with CATCH 22. Eur J Pediatr (1996) 155:425-426
  • Hasegawa T, Hasegawa Y, Takada M, Tsuchiya Y, Iwashita M: Increased free form of insulin-like growth factor-I in circulation throughout normal human pregnancy. Endocr J 43 (1996) Suppl:S75-76
  • Hasegawa T, Ogata T, Hasegawa Y, Honda M, Nagai T, Fukushima Y, Nakahori Y, Matsuo N: Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata. Hum Genet (1996) 97:564-567
  • Hasegawa Y, Hasegawa T, Anzo M, Aso T, Tsuchiya Y: Clinical utility of insulin-like growth factor-I (IGF-I) and IGF binding protein-3 levels in the diagnosis of GH deficiency (GHD) during childhood. Endocr J 43 (1996) Suppl:S1-4
  • Hasegawa Y, Hasegawa T, Takada M, Tsuchiya Y: Plasma free insulin-like growth factor I concentrations in growth hormone deficiency in children and adolescents. Eur J Endocrinol (1996) 134:184-189
  • Honda M, Iitaka K, Kawaguchi H, Hoshii S, Akashi S, Kohsaka T, Tuzuki K, Yamaoka K, Yoshikawa N, Karashima S, Itoh Y, Hatae K.: The Japanese national registry data on pediatric CAPD patients: a ten-year experience. A report of The Study Group Of Pediatric PD Conference. Peri Dial Int (1996) 16:269-275
  • Ikeda K, Shaw White JR, Wert SE, Whitsett JA: Hepatocyte nuclear factor 3 activates transcription of thyroid transcription factor 1 in respiratory epithelial cells. Mol Cell Biol (1996) 16:3626-3636
  • Imasaki K, Hasegawa T, Ishizaka H, Okabe T, Hasegawa Y, Takayanagi R, Nawata H.: Sporadic Reifenstein syndrome due to a de novo mutation (746Val→Met) of the androgen receptor. Clin Pediatr Endocrinol (1996) 5:1-9
  • Iseki M, Sasaki T, Kenri T, Okazaki N, Yamashita R, Shintani M, Sasaki Y, Yayoshi M: Epidemiological study of Mycoplasma pneumoniae infections in Japanese on PCR-restriction fragment length polymorphism of the P1 cytadhesin gene J Clin Microbiol (1996) 34:447-449
  • Iseki M, Takahashi T, Kimura K, Yamashita R, Sasaki T: Number of specific antibody-secreting cells in the peripheral blood among children with Mycoplasma pneumonia Infect Immun (1996) 64:2799-2803
  • Kawai H, Aoyama T, Murase Y, Tamura C, Imaizumi A: A causal relationship between Bordetella pertussis and Bordetella parapertussis infections. Scand J Infect Dis (1996) 28:377-381
  • Kawasaki H, Mori T, Takekuma K, Hoshika A, Hata M, Nakayama T: Polymerase chain reaction detection of the hemaglutinin gene from an attenuated measles vaccine strain in the peripheral mononuclear cells of children with autoimmune hepatitis Arch Virolo (1996) 141:877-884
  • Kawashima H, Miyajima T, Mori T, Yuan L, Ogihara M, Kinoue K, Takekuma K, Hoshika A: A case of intractable epilepsy positive for the detection of measles virus genome in the cerebrospinal fluid and peripheral mononuclear cells using reverse transcriptase-polymerase chain reaction. Brain & Development (1996) 18:220-223
  • Kelley RL, Roessler E, Hennekam RC, Feldman GL, Kosaki K, Jones MC, Palumbos JC, Muenke M: Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog? Am J Med Genet (1996) 66:478-484
  • Kojika S, Sugita K, Inukai T, Saito M, Iijima K, Tezuka T, Goi K, Shiraishi K, Mori T, Okazaki T, Kagami K, Ohyama K, Nakazawa S: Mechanisms of glucocorticoid resistance in human leukemic cells : implication of abnormal 90 and 70kDa heat shock proteins Leukemia (1996) 10:994-999
  • Kondoh S, Ito M: Seasonal variation in the circadian rhythm of pulmonary function in stable asthmatic children who have nearly outgrown their asthma Chronobiol Int (1996) 13:295-303
  • Kosaki K, Jones MC, Stayboldt C: Zimmer phocomelia: delineation by principal coordinate analysis. Am J Med Genet (1996) 66:55-59
  • Kosaki K, Mendoza A, Jones KL: Cervical flexion: its contribution to normal and abnormal cardiac morphogenesis. Teratology (1996) 54:135-144
  • Lee MM, Donahoe PK, Hasegawa T, Silverman B, Crist GB, Best S, Hasegawa Y, Noto RA, Schoenfeld D, MacLaughlin DT: Mullerian inhibiting substance in humans: normal levels from infancy to adulthood. J Clin Endocrinol Metab (1996) 81:571-576
  • Matsuo N: Fetal testis formation: a critical event for sex determination and differentiation. Acta Paediatr Jpn (1996) 38:377-379
  • Miyamoto H, Jozaki K, Kikuchi H: Congenital, self-healing reticulohistiocytosis : report of a case with multiple, localized lesions Eur J Dermatol (1996) 6:389-391
  • Muroya K, Ogata T, Matsuo N, Nagai T, Franco B, Ballabio A, Rappold G, Sakura N, Fukushima Y: Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus. Am J Med Genet (1996) 64:583-587
  • Nishimura G, Hasegawa T, Nagai T: A propositus with Weaver syndrome and his mildly affected mother: Implication of nontraditional inheritance? Am J Med Genet (1996) 65:249-251
  • Nishimura G, Sato S, Ogata T, Tamai S, Hasegawa T, Matsuo N: A case of skeletal dysplasia with advanced carpal ossification and "monkey wrench" appearance of the femora: mild Desbuquois dysplasia? Eur J Pediatr (1996) 155:1040-1042
  • Ogata T, Matsuo N: Sex determining gene on the X chromosome short arm: dosage sensitive sex reversal. Acta Paediatr Jpn (1996) 38:390-398
  • Okuyama T, Huber RM, Bowling W, Pearline R, Kennedy SC, Flye MW, Ponder KP.: Liver-directed gene therapy: a retroviral vector with a complete LTR and the apoE enhancer-a1-antitrypsin promoter dramatically increases expression of human a1- antitrypsin in vivo. Hum Gene Ther (1996) 7:637-645
  • Sakaguchi M, Nakayama T, Inouye S: Food allergy to gelatin in children with systemic immediate-type reactions, including anaphylaxis, to vaccines. J Allergy Clin Immunol (1996) 98:1058-1061
  • Sato S, Anzo M, Hasegawa T, Kamimaki T, Matsuo N.: Short term growth hormone treatment for a girl with osteodysplastic primordial dwarfism type?. Clin Pediatr Endocrinol 5(Suppl (1996) 8):139-141
  • Stams T, Nair SK, Okuyama T, Waheed A, Sly WS, Christianson DW: Crystal structure of the secretory form of membrane-associated human carbonic anhydrase IV at 2.8-A resolution. Proc Natl Acad Sci USA (1996) 93:13589-13594
  • Sugaya N, Kusumoto N, Suzuki Y, Nerome R, Nerome K: Large sequential outbreaks caused by influenza A (H3N2) and B viruses in an institution for the mentally handicapped. J Med Virol (1996) 50:120-125
  • Takahashi T, Nowakowski RS, Caviness VS Jr: Interkinetic and migratory behavior of a cohort of neocortical neurons arising in the early embryonic murine cerebral wall. J Neurosci (1996) 16:5762-5776
  • Takahashi T, Nowakowski RS, Caviness VS Jr: The leaving or Q fraction of the murine cerebral proliferative epithelium: a general model of neocortical neuronogenesis. J Neurosci (1996) 16:6183-6196
  • Takuma Y, Seki T: Combination therapy of infantile spasms with high-dose pyridoxal phosphate and low-dose corticotropin. J Child Neurol (1996) 11:35-40
  • Tamai S, Cody LB, Sly WS: Molecular cloning of the mouse gene coding for carbonic anhydrase IV. Biochem Genet (1996) 34:31-43
  • Tamai S, Waheed A, Cody LB, Sly WS: Gly-63-->Gln substitution adjacent to His-64 in rodent carbonic anhydrase IVs largely explains their reduced activity. Proc Natl Acad Sci USA (1996) 93:13647-13652
  • Tsunawaki S, Kagara S, Yoshikawa K, Yoshida L, Kuratsuji T: nvolvement of p40phox in activation of phagocyte NADPH oxidase through association of its carboxyl-terminal, but not its amino-terminal, with p67phox. J Exp Med (1996) 184:893-902
  • Waheed A, Okuyama T, Heyduk T, Sly WS: Carbonic anhydrase IV: purification of a secretory form of the recombinant human enzyme and identification of the positions and importance of its disulfide bonds. Arch Biochem Biophys (1996) 333:432-438
  • Yamagishi H, Kato S, Hiraishi Y, Ishihara T, Hata J, Matsuo N, Takano T: Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene. J Med Genet (1996) 33:1027-1031
  • Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A, Nakamura M, Sano A, Komure O, Kondo I, Jin DK, Sorensen SA, Potter NT, Young SR, Nakamura K, Nukitna N, Nagao Y, Tadokoro K, Okuyama T, Miyashita T, Inoue T, Kanazawa I, Yamada M: A uniqe origin andYanagisawa multistep process for the generation of expanded DRPLA triplet repeats Hum Mol Genet (1996) 5:373-380