Publications 1999

Yokoya S, Araki K, Igarashi Y, Kohno H, Nishi Y, Hasegawa Y, Fujita K, Iwatani N, Tachibana K, Ohyama Y, Seino Y, Satoh M, Fujieda K, Tanaka T.: High-dose growth hormone (GH) treatment in prepubertal GH-deficient children. Acta Paediatrica Supplement. (1999) 88:76-79
Akamatsu W, Okano H, Osumi N, Inoue T, Nakamura S, Sakakibara S, Miura M, Matsuo N, Darnell R, Okano H: Mammalian ELAV-like neuronal RNA-binding proteins HuB and HuC promote neuronal development in both the central and the peripheral nervous systems Proc Nat Acad Sci USA (1999) 96:9885-9890
Anzo M, Hasegawa Y, Satoh S, Matsuo N, Satoh K, Mitani H, Ashizawa K, Ohtsuki F, Satoh M, Tanaka T, Matsuoka H, Murata M.: An automatic bone age rating system in the study of Turner syndrome. Clin Pediatr Endocrinol 8(suppl (1999) 12):71-74
Asano T, Tatsuma N, Yoshida J, Ohashi R, Ambo K, Tsuchiya M, Murakami M, Yamanaka N, Honda M, Yamamoto M.: Association of angiotensin-converting enzyme gene polymorphism and renal pathology in Japanese children with IgA nephropathy Clin Nephrol (1999) 51:335-340
Awazu M, Ishikura K, Hida M, Hoshiya M: Mechanisms of mitogen-activated protein kinase activation in experimental diabetes. J Am Soc Nephrol (1999) 10:738-745
Campo MD, Kosaki K, Jones K: Developmental delay in fetal aminopterin/methotrexate syndrome Teratology (1999) 60:10-12
Cao G, Zhao L, Stangl H, Hasegawa T, Richardson JA, Parker KL, Hobbs HH: Developmental and hormonal regulation of murine scavenger receptor, class B, type 1. Mol Endocrinol (1999) 13:1460-1473
Caviness VS Jr, Takahashi T, Nowakowski RS: The G1 restriction point as critical regulator of neocortical neuronogenesis. Neurochem Res (1999) 24:497-506
Daly TM, Okuyama T, Vogler C, Haskins ME, Muzyczka N, Sands MS.: Neonatal intramuscular injection with recombinant adeno-associated virus results in prolonged beta-glucuronidase expression in situ and correction of liver pathology in mucopolysaccharidosis type VII mice. Hum Gene Ther (1999) 10:85-94
Del Campo M, Kosaki K, Bennett FC, Jones KL: Developmental delay in fetal aminopterin/methotrexate syndrome. Teratology (1999) 60:10-12
Del Campo M, Kosaki K, Bennett FC, Jones KL: Developmental delay in fetal aminopterin/methotrexate syndrome. Teratology (1999) 60:10-12
Delalle I, Takahashi T, Nowakowski RS, Tsai LH, Caviness VS Jr: Cyclin E-p27 opposition and regulation of the G1 phase of the cell cycle in the murine neocortical PVE: a quantitative analysis of mRNA in situ hybridization. Cereb Cortex (1999) 9:824-832
Fujino M, Li XK, Okuyama T, Funeshima N, Tamura A, Enosawa S, Kita Y, Amano T, Yamada M, Amemiya H, Suzuki S: On/off switching Fas-ligand gene expression in liver by Cre/Loxp adenovirus vector system. Transplant Proc (1999) 31:753-754
Fujino M, Okuyama T, Li XK, Funeshima N, Tamura A, Enosawa S, Amano T, Amemiya H, Suzuki S.: Controlled Fas ligand gene expression by Cre/loxP-mediated switching system: high levels of FasL expression result in lethal hepatitis. Transplant Proc (1999) 31:2695-2696
Hagiwara K, Miura R, Kosaki R, Berglund E, Ranscht B, Yamaguchi Y: Immunohistochemical evidence for the brevican-tenascin-R interaction: colocalization in perineuronal nets suggests an physiological role for the interaction in the adult rat brain J Compar Neurol 26 (1999) 410:256-264
Hagiwara K, Miura R, Kosaki R, Berglund E, Ranscht B, Yamaguchi Y: Immunohistochemical evidence for the brevican-tenascin-R interaction: colocalization in perineuronal nets suggests an physiological role for the interaction in the adult rat brain J Compar Neurol (1999) 26:256-264
Hanabusa H, Tagami H, Hataya H.: Renal atrophy associated with long-term treatment with indinavir. N Engl J Med (1999) 340:392-393
Hasegawa T, Harada N, Ikeda K, Ishii T, Hokuto I, Kasai K, Tanaka M, Fukuzawa R, Niikawa N, Matsuo N: Digynic triploid infant surviving for 46 days. Am J Med Genet (1999) 87:306-310
Hasegawa T, Kozlowski K, Nishimura G, Hara H, Hasegawa Y, Aso T, Koto S, Nagai T, Tsuchiya Y.: Spondylo-metaphyseal dysplasia with regressive platyspondyly. Locomotor System (1999) 6:53-59
Hasui M, Kuratsuji T and the Study Group of Phagocyte Disorders of Japan : Chronic Granulomatous Disease in Japan : Incidence and Natural History. Pediatr Int (1999) 41:589-593
Hataya H, Ikeda M, Ide Y, Kobayashi Y, Kuramochi S, Awazu M: Distal tubular dysfunction in lupus nephritis of childhood and adolescence. Pediatr Nephrol (1999) 13:846-849
Honda M: The 1997 report of the Japanese national registry data on pediatric peritoneal dialysis patients Peri Dial Int (1999) 19:473-478
Ikegawa S, Masuno M, Kumano Y, Okawa A, Somura M, Koyama K, Okui K, Makita Y, Sasaki M, Kohdera U, Okuda M, Koyama H, Ohashi H, Tajeri H, Imaizumi K, Nakamura Y: Cloning of translocation breakpoints associated with Shwachman sndrome and jdentification of a candidate gene Clini Genet (1999) 55:466-472
Ishii E, Yoshida N, Kimura N, Fujimoto J, Mizutani S, Sako M, Hibi S, Nagano M, Yoshida T, Mori T, Kiyokawa N, Mohri S, Tanaka T, Miyazaki S, Hara T.: Clonal dissemination of T-lymphocytes in scid mice from familial hemophagocytic lymphohistiocytosis. Med Pediatr Oncol (1999) 32:201-208
Ishii T, Sato S, Anzo M, Sasaki G, Hasegawa T, Tamai S, Matsuo N: Treatment with a gonadotropin-releasing-hormone analog and attainment of full height potential in a male monozygotic twin with gonadotropin-releasing hormone-dependent precocious puberty. Eur J Pediatr (1999) 158:933-935
Ishikawa M, Yokoya S, Tachibana K, Hasegawa Y, Yasuda T, Tokuhiro E, Hashimoto Y, Tanaka T: Serum levels of 20-kilodalton human growth hormone (GH) are parallel those of 22-kilodalton human GH in normal and short children. J Clin Endocrin Metab (1999) 84:98-104
Ishizuka B, Kudo Y, Amemiya A, Yamada H, Matsuda T, Ogata, T: Anti-nuclear antibodies in patients with premature ovarian failure. Human Reproduction (1999) 14:70-75
Ito B, Kumagai M, Manabe A, Coustan-Smith E, Raimondi SC, Behm FG, Murti KG, Rubnitz JE, Pui CH, Campana D: Hyperdiploid acute lymphoblastic leukemia with 51 to 65 chromosomes : a distinct biological entity with a marked propensity to undergo apoptosis Blood (1999) 93:315-320
Ito S, Ikeda M, Takata A, Kikuchi H, Hata J, Honda M: Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years. Pediatr Nephrol (1999) 13:790-791
Kakinuma Y, Hama H, Kasuya Y, Fukamizu A.: A new aspect of renin-angiotensin system in central nervous system. Recent Research Development in Neurochemistry (1999) 2:Part II, 473-493
Kakinuma Y, Miyauchi T, Kobayashi T, Yuki K, Maeda S, Sakai S, Yamaguchi I, Goto K.: Myocardial expression of endothelin-2 is altered reciprocally to that of endothelin-1 during ischemia of cardiomyocytes in vitro and during heart failure in vivo. Life Science (1999) 65:1671-1683
Kakinuma Y, Miyauchi T, Yuki K, Murakoshi N, Goto K, Yamaguchi I.: Hypoxia-inducible factor (HIF)-1α, which activates glycolytic system adaptively in the impaired energy metabolism, maladaptively increases emdothelin-1 mRNA expression in the failing heart. Circulation (1999) 100:I-2206
Kakinuma Y, Sugiyama F, Taniguchi K, Horiguchi H, Ogata T, Murakami K, Yagami K, Fukamizu A.: Developmental stage-specific involvement of angiotensin in murine nephrogenesis. Pediatric Nephrology (1999) 13:792-799
Kashiwagi Y, Takami T, Mori T, Nakayama T: Sequence analysis of F, SH, and HN genes among mumps virus strains in Japan . Arch Virol (1999) 144:593-599
Katagiri YU, Mori T, Nakajima H, Katagiri C, Taguchi T, Takeda T, Kiyokawa N, Fujimoto J.: Activation of Src family kinase Yes induced by Shiga toxin binding to globotriaosyl ceramide (Gb3/CD77) in low density, detergent-insoluble microdomains. J Biol Chem (1999) 274:35278-35282
Kikuchi S, Tanoue A, Goda N, Matsuo N, Tsujimoto G: Structure and sequence of the Mouse V1a and V1b vasoperssin receptor genes. Jpn J Pharmacol (1999) 81:388-392
Kitamura T, Kitamura F, Mitsuhashi T, Ito A, Okazaki Y, Okuda N, Katoh H. Image of psychiatric patients’ competency to give informed consent to treatment in Japan. I. A factor analytic study. Intetnatinal Journal of Law and Psychiatry (1999) 22:45-
Kitamura T, Kitamura F, Ito A, Okazaki Y, Okuda N, Mitsuhashi T, Katoh H. Image of psychiatric patients’ competency to give informed consent to treatment in Japan. II. A case vignette study of competency judgments. International Journal of Law and Psychiatry (1999) 22:133-42.
Kitanaka A, Suzuki T, Ito C, Nishigaki H, Coustan-smith E, Tanaka T, Kubota Y, Campana D: CD38-mediated signaling events in murine pro-B cells expressing human CD38 with or without its cytoplasmic domain J Immun (1999) 162:1952-1958
Kohda E, Saeki M, Nakano N, Masaki H, Ogawa
K, Nirasawa M, Hiramatsu H: Congenital absence of the portal vein in a boy. Pediatric Radiology (1999) 29: 235-237
Kosaki K, Bassi MT, Kosaki R, Lewin M, Belmont J, Schauer G, Casey B: Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development. Am J Hum Genet (1999) 64:712-721
Kosaki R, Gebbia M, Kosaki K, Lewin M, Bowers P, Towbin JA, Casey B: Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB. Am J Med Genet (1999) 82:70-76
Kosaki R, Watanabe K, Yamaguchi Y: Overproduction of hyaluronan by expression of the hyaluronan synthase Has2 enhances anchorage-independent growth and tumorigenicity Cancer Res (1999) 59:1141-1145
Kosho T, Muroya K, Nagai T, Fujimoto M, Yokoya S, Sakamoto H, Hirano T, Terasaki H, Ohashi H, Nishimura G, Sato S, Matsuo N, Ogata T: Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome. J Clin Endocrinol Metab (1999) 84:4613-4621
Kure H, Suzuki Y, Hasegawa Y, Hara Y, Inoue T, Kida Y, Matsubara Y, Narisawa K: Molecular analysis of glycogenstorage disease type Ib : Structual and mutational analysis of the gene encoding microsomal glucose-6-phosphate transporter Amer J Med Gen (1999) 86:253-257
Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T: Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature. Am J Med Genet (1999) 86:44-50
Matsuoka S, Awazu M.: Reply to the letter from M. Bald. Pediatr Nephrol (1999) 13:997
Miyauchi J, Asada M, Tsunematsu Y, Kaneko Y, Kojima S, Mizutani S.: Abnormalities of the p53 gene in juvenile myelomonocytic leukaemia. Br J Haemat (1999) 106:980-986
Mori Y, Jing P, Kayama M, Fujieda K, Hasegawa T, Nogimori T, Hirooka Y, Mitsuma T.: Gene amplification as a common cause of inherited thyroxine-binding globulin excess: analysis of one familial and two sporadic cases. Endocr J (1999) 46:613-619
Morikawa N, Namba S, Fujii Y, Satoh Y, Fukuba K.: Intrauterine volvulus without malrotation associated with segmental absence of small intestinal musculature. J Pediatr Surg (1999) 34:1549-51
Muroya K, Ishii T, Nakahori Y, Asakura Y, Tachibana K, Masuno M, Imaizumi K, Tanaka Y, Kawada Y, Yukizane S, Ogata T: Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: molecular analysis in four patients. Genes Chromosomes Cancer (1999) 25:40-45
Muroya K, Kinoshita E, Kamimaki T, Matsuo N, Yorifugi T, Ogata T: Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11. J Med Genet (1999) 36:187-191
Muroya K, Kosho T, Ogata T, Matsuo M: Female carriers of Xp22.3 deletion including MRX locus. Am J Med Genet (1999) 84:384-385
Nakadate H, Tsuchiya T, Maseki N, Hatae Y, Tsunematsu Y, Horikoshi Y, Ishida Y, Kikuta A, Eguchi H, Endo M, Miyake M, Sakurai M, Kaneko Y.: Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor. Genes (1999) 25:26-32
Nakata Y, Mori T, Yamazaki T, Suzuki T, Okazaki T, Kurosawa Y, Kinoshita A, Ohyashiki K, Nakazawa S: Acute myeloid leukemia with hypergranular cytoplasm accompanied by t(X;11)(q24;q23) and rearrangement of the MLL gene. Leuk Res (1999) 23:85-88
Nakayama T, Aizawa X, Kuno-Sakai H: A clinical analysis of gelatin allergy and determination of its causal relationship to the previous administration of gelatin-containing acellular pertussis vaccine combined with diphtheria and tetanus toxoids. J Allergy & Clin Immunol (1999) 103:321-325
Nanao K, Anzo M, Hasegawa Y.: Morning hypoglycemia leading to death in a child with congenital hypopituitarism. Acta Paediatr (1999) 88:1173
Nanao K, Miyamoto J, Anzo M, Tsukuda T, Hasegawa Y: A case of congenital hypopituitarism: difficulty in the diagnosis of ACTH deficiency due to high serum cortisol levels from a hypothyroid state. Endocr J (1999) 46:183-186.
Nishimoto G, Zelenina M, Li D, Yasui M, Aperia A, Nielsen S, Nairn AC: Arginine vasopressin stimulates phosphorylation of aquaporin-2 in rat renal tissue Amer J Physiol (1999) 276:254-259
Nishimura K, Hara M.: Pathogenetic role of monoamine metabolism in complex febrile seizures. Pediatr Neurol (1999) 21:553-556
Nishiyama M, Arai Y, Tsunematsu Y, Kobayashi H, Asami K, Yabe M, Kato S, Oda M, Eguchi H, Ohki M, Kaneko Y: 11p15 Translocations involving the NUP98 gene in childhood therapy-related acute myeloid leukemia/ myelodysplastic syndrome. Genes, Chromosomes & Cancer (1999) 26:215-220
Ogata T: SHOX: pseudoautosomal homeobox containing gene for short stature and dyschondrosteosis. Growth Horm IGF Res 9 Suppl (1999) B:53-57
Oishi T, Sugiura W, Matsuda M, Abumi H, Okano A, Yamada K, Koike M, Taki M, Miura T, Fukutake K, Gouchi K, Ajisawa A, Iwamoto A, Hanabusa H, Miyama J, Takamatsu J, Takata N, Kakishita E, Higasa S, Yoshioka A, Kashiwagi S, Shirahata A and Nagai Y: Status of Anti-HIV-1 Chemotherapy in Japan. Jpn J Infect Dis (1999) 52:51-52
Okita H, Umezawa A, Fukuma M, Ando T, Urano F, Sano M, Nakata Y, Mori T, Hata J.: Acute myeloid leukemia possessing jumping translocation is related to highly elevated levels of EAT/mcl-1, a Bcl-2 related gene with anti-apoptotic functions. Leukemia Res (1999) 24:73-77
Seino Y, Moriwake T, Tanaka H, Inoue M, Kanzaki S, Tanaka T, Matsuo N, Niimi H.: Molecular defects in achondroplasia and the effects of growth hormone treatment. Acta Paediatrica Supplement (1999) 88:118-120
Sonoda S, Gotoh Y, Bann F, Nakayama T: Acute lower respiratory infections in hospitalized children over a 6 year period in Tokyo. Pediatr Int (1999) 41:519-24
Srivastava D, Yamagishi H: Reply: role of the dHAND-UFD1L pathway Trends Genet (1999) 15:253-254
Sugano K, Taniguchi T, Saeki M, Tsunematsu Y, Tomaru U, Shimoda T.: Germline p53 mutation in a case of Li-Fraumeni syndrome presenting gastric cancer. Jpn J Clin Oncol (1999) 29:513-516
Sugaya N, Miura M: Amnatadine therapy for influenza type A-associated encephalopathy Ped Infect Dis J (1999) 18:734
Sugiura W, Matsuda M, Abumi H, Yamada K, Taki M, Ishikawa M, Miura T, Fukutake K, Gouchi K, Ajisawa A, Iwamoto A, Hanabusa H, Miyama J, Takamatsu J, Takata N, Kakishita E, Yoshioka A, Kashiwagi S, Shirahata A and NagaI Y: Prevalence of Drug Resistance-Related Mutations among HIV-1s in Japan. Jpn J Infect Diseas (1999) 52:21-22
Sugiura W, Oishi T, Okano A, Matsuda M, Abumi H, Yamada K, Koike M, Taki M, Ishikawa M, Miura T, Fukutake K, Gouchi K, Ajisawa A, Iwamoto A, Hanabusa H, Miyama J, Takamatsu J, Takata N, Kakishita E, Higasa S, Kashiwagi S, Shirahata A, Nagai Y: Two Possible Pathways for Acquisition of Mutations Related to Nelfinavir Resistance. Jpn J Infect Diseas (1999) 52:175-176
Suzuki H, Delano FA, Jamshidi N, Katz D, Mori M, Kosaki K, Gottlieb RA, Ishii H, Schmid Schonbein GW: Enhanced DNA fragmentation in the thymus of spontaneously hypertensive rats. Am J Physiol (1999) 276:H2135-2140
Tachibana A, Kato T, Ejima Y, Yamada T, Shimizu T, Yang L, Tsunematsu Y, Sasaki S.: The FANCA gene in Japanese Fanconi anemia: Reports of eight novel mutations and analysis of sequence variability. Human Mutation (1999) 13:237-244
Takahashi M, Saito H, Okuyama T, Miyashita T, Kosuga M, Sumisa F, Yamada M, Ebinuma H, Ishii H: Overexpression of Bcl-2 protects human hepatoma cells from Fas-antibody-mediated apoptosis. J Hepatol (1999) 31:315-322
Takahashi T, Bhide PG, Goto T, Miyama S, Caviness VS Jr: Proliferative behavior of the murine cerebral wall in tissue culture: cell cycle kinetics and checkpoints. Exp Neurol (1999) 156:407-417
Takahashi T, Goto T, Miyama S, Nowakowski RS, Caviness VS Jr: Sequence of neuron origin and neocortical laminar fate: relation to cell cycle of origin in the developing murine cerebral wall. J Neurosci (1999) 19:10357-10371
Takahashi T, Nowakowski RS, Caviness VS Jr.: Cell cycle as operational unit of neocortical neuronogenesis. Neuroscientist (1999) 5:155-163
Takayama S, Miura T, Matsuo S, Taki M, Sugii S: Prevalence and persistence of a novel DNA TT virus (TTV) infection in Japanese haemophiliacs. Br J Haematol (1999) 104:626-629
Takayama S, Miura T, Tominaga T, Taki M, Matsuo S, Sugii S, Shimotohno K: Partial nucleotide sequencing of the NS3/helicase region of hepatitis G virus to prove vertical transmission. FEMS Microbiology Letters (1999) 175:273-279
Takiyama N, Dunigan JT, Vallor MJ, Kase R, Sakuraba H, Barranger JA.: Retrovirus-mediated transfer of human α-galactosidase A gene to human CD34+ hematopoietic progenitor cells. Hum Gene Ther (1999) 10:2881-2889
Tokieda K, Ikegami M, Wert S, Baatz J, Zou Y, Whitsett J: Surfactant protein B corrects oxygen-induced pulmonary dysfunction in heterozygous surfactant protein B-deficient mice Ped Res (1999) 46:708-714
Tokieda K, Iwamoto HS, Bachurski C, Wert SE, Hull WM, Ikeda K, Whitsett JA: Surfactant protein-B-deficient mice are susceptible to hyperoxic lung injury. Am J Respir Cell Mol Biol (1999) 21:463-472
Tokieda K, Morikawa Y, Maeyama K, Mori K, Ikeda K: Clinical manifestations of Bacillus cereus meningitis in newborn infants. J Paediatr Child Health (1999) 35:582-584
Uchida H, Kiyokawa N, Taguchi T, Horie H, Fujimoto J, Takeda T: Shiga toxins induce apoptosis in pulmonary epithelium derived cells. J Infec Dis (1999) 180:1902-1911
Watanabe H: Infant Mental Health in Japan Asian Ｍed (1999) :J
Watanabe H: Trouble precoce de l’attachement et retablissement des liens mere-bebe: cas d’un bebe d’une mere abandonnee dans sa petite enfance. Cahier Psychiatriques (1999) 26:117-127
Yamada M, Hasegawa T, Hasegawa Y: Absence of proteolysis of insulin-like growth factor binding protein-3 in serum from patients with growth hormone deficiency. Endocr J (1999) 46:717-722
Yamada S, Tomura H, Nishigori H, Sho K, Mabe H, Iwatani N, Takumi T, Kito Y, Moriya N, Muroya K, Ogata T, Onigata K, Morikawa A, Inoue I, Takeda J: Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins. Diabetes (1999) 48:645-648
Yamagishi H, Garg V, Matsuoka R, Thomas T, Srivastava D: A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. Science (1999) 283:1158-1161
Yamaguchi Y, Awazu M, Matsuoka S, Maeda J, Tokumura M, Kojima Y, Matsuo N: White coat hypertension in two adolescents. Pediatr Nephrol (1999) 13:60-62
Yasui M, Hazama A, Kwon TH, Nielsen S, Guggino WB, Agre P: Rapid gating and anion permeability of an intracellular aquaporin Nature (1999) 402:184-187
Yasui M, Kwon TH, Knepper MA, Nielsen S, Agre P: Aquaporin-6: An intracellular vesicle water channel protein in renal epithelia Proc Natl Acad Sci USA (1999) 96:5808-5813
Yoshikawa N, Ito H, Sakai T, Takekoshi Y, Honda M, Awazu M, Ito K, Iitaka K, Koitabashi Y, Yamaoka K, Nakagawa K, Nakamura H, Matsuyama S, Seino Y, Takeda N, Hattori S, Ninomiya M.: A controlled trial of combined therapy for newly diagnosed severe childhood IgA nephropathy. The Japanese Pediatric IgA Nephropathy Treatment Study Group. J Am Soc Nephrol (1999) 10:101-109