Publications 2005

  • Akamatsu W, Fujihara H, Mitsuhashi T, Yano M, Hayakawa Y, Okano HJ, Sakakibara S, Takano H, Takano T, Takahashi T, Noda T, Okano H. 2005. RNA-binding protein HuD regulates neuronal cell identity and maturation. Proc Natl Acad Sci U S A, 102:4625-30.
  • Aramaki M, Hokuto I, Matsumoto T, Ishimoto H, Inoue M, Kimura T, Oikawa Y, Ikeda K, Yoshimura Y, Takahashi T, Kosaki K. Iridic and Retinal Coloboma Associated With Prenatal Methimazole Exposure. Am J Med Genet (in press).
  • Chiba N, Kobayashi R, Hasegawa K, Morozumi M, Nakayama E, Tajima T, Iwata S, Ubukata K, Group ARDS. Antibiotic susceptibility according to genotype of penicillin-binding protein and macrolide resistance genes, and serotype of Streptococcus pneumoniae isolates from community-acquired pneumonia in children. J Antimicrob Chemother 2005;56:756-760.
  • Choe M-s, Sato A, Watanabe H, Hasegawa T. The correlation between insulin-like growth factor-I and obesity index during inpatient treatment in anorexia nervosa in childhood and adolescence. Clin Pediatr Endocrinol 2005;14:21-23.
  • Fujino M, Yoshida N, Yamaguchi S, Hosaka N, Ota Y, Notomi T, Nakayama T. A simple method for the detection of measles virus genome by loop-mediated isothermal amplification (LAMP). J Med Virol 2005;76:406-413.
  • Fukami M, Hasegawa T, Horikawa R, Ohashi T, Nishimura G, Homma K, Ogata T. Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency. Pediatr Res 2005;59:276-280.
  • Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. 2005. Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients. J Clin Endocrinol Metab, 90:414-426.
  • Fukami M, Okuyama T, Yamamori S, Nishimura G, Ogata T. 2005. Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: implication for the SHOX enhancer. Am J Med Genet A;137:72-76.
  • Futatsugi A, Nakamura T, Yamada MK, Ebisui E, Nakamura K, Uchida K, Kitaguchi T, Takahashi-Iwanaga H, Noda T, Aruga J, Mikoshiba K. 2005. IP3 Receptor Types 2 and 3 Mediate Exocrine Secretion Underlying Energy Metabolism. Science, 309:2232-2234.
  • Hayakawa K, Nagamine T, Li X-K, Katsumata N, Ogata T, Tanaka T. Affinity chromatographic determination of D-aspartic acid in the liver cell lines. Trends in Chromatography 2005;1:105-110.
  • Hirokane K, Tokumura M, Nanri S, Kimura K, Saito I. Influences of mothersﾒ dieting behaviors on their junior high school daughters. Eat Weight Disord 2005;10:162-167.
  • Hori N, Inokuchi M, Yoshida R, Sato A, Choe M-S, Watanabe H, Hasegawa T. 2005. Resumption of mensturation and nutritional status in female patients with early onset anorexia nervosa. Clin Pediatr Endocrinol, 14:73-76.
  • Igarashi S, Manabe A, Ohara A, Kumagai M, Saito T, Okimoto Y, Kamijo T, Isoyama K, Kajiwara M, Sotomatsu M, Sugita K, Sugita K, Maeda M, Yabe H, Kinoshita A, Kaneko T, Hayashi Y, Ikuta K, Hanada R, Tsuchida M. No advantage of dexamethasone over prednisolone for the outcome of standard- and intermediate-risk childhood acute lymphoblastic leukemia in the Tokyo Children’s Cancer Study Group L95-14 protocol. J Clin Oncol 2005;23:6489-6498.
  • Ishikura K, Fujita H, Hida M, Awazu M. 2005. Trapidil inhibits platelet-derived growth factor-induced migration via protein kinase A and RhoA/Rho-associated kinase in rat vascular smooth muscle cells. Eur J Pharmacol, 515:28-33.
  • Jin L, Rima B, Brown D, Orvell C, Tecle T, Afzal M, Uchida K, Nakayama T, Song J-W, Kang C, Rota P, Xu W, Featherstone D. Proposal for genetic characterisation of wild-type mumps strains: preliminary standardisation of the nomenclature. Arch Virol 2005;150:1903-1909.
  • Kagami M, Nishimura G, Okuyama T, Hayashidani M, Takeuchi T, Tanaka S, Ishino F, Kurosawa K, Ogata T. 2005. Segmental and full paternal isodisomy for chromosome 14 in three patients: Narrowing the critical region and implication for the clinical features. Am J Med Genet, A138:127-32.
  • Kanda T, Hayashi K, Wakino S, Homma K, Yoshioka K, Hasegawa K, Sugano N, Tatematsu S, Takamatsu I, Mitsuhashi T, Saruta T. 2005. Role of Rho-kinase and p27 in Angiotensin II-Induced Vascular Injury. Hypertension, 45:724-729.
  • Kinai E, Hanabusa H. Renal tubular toxicity associated with tenofovir assessed using urine-beta 2 microglobulin, percentage of tubular reabsorption of phosphate and alkaline phosphatase levels. AIDS 2005;19:2031-2033.
  • Kosaki K, Takahashi D, Udaka T, Kosaki R, Matsumoto M, Ibe S, Isobe T, Tanaka Y, Takahashi T. Molecular Pathology of Shprintzen-Goldberg Syndrome. Am J Med Genet (in press).
  • Kosaki K, Udaka T, Okuyama T. DHPLC in clinical molecular diagnostic services. Mol Genet Metab 2005;86:117-123.
  • Kosaki K, Yamaghishi C, Sato R, Semejima H, Fuijita H, Tamura K, Maeyama K, Yamagishi H, Sugaya A, Dodo H, Tanigawara Y, Takahashi T. Polymorphism in VKORC1 modulates the required warfarin dose. Pediatr Cardiol (in press).
  • Kosaki R, Higuchi M, Mitsui N, Matsushima K, Ohashi H, Kosaki K. 2004. Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p? Congenit Anom, 45:35-8.
  • Kosaki R, Kosaki K, Kawashima N, Ueoka K, Fukuhara Y, Kosuga M, Honna T, Okuyama T. OEIS compelx With del(q12.2q13.2). 2005. Am J Med Genet, 135:224-226.
  • Kosaki R, Kosaki K, Matsushima K, Mitsui N, Matsumoto N, Ohashi H. 2005. Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplication. Congenit Anom, 45:62-4.
  • Kuroda T, Honna T, Morikawa N, Kitano Y, Fuchimoto Y, Terawaki K, Kumagai M, Tsunematsu Y, Masaki H, Matsuoka K, Saeki M. Tumor cell dynamics and metastasis in advanced neuroblastoma. Pediatr Surg Int 2005;21:859-863.
  • Liu S, Ogata T, Maruyama T, Yoshimura Y, Ishizuka B. Association of common LH variant with hyperfunctional promoter in a Japanese infertile woman. Endocrine J 2005;52:781-784.
  • Matsubara K, Yabe H, Ogata T, Yoshida R, Fukuya T. 2005. Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation. Am J Hematol, 79:171-172.
  • Miura M, Garcia FL, Crawford SE, Rowley AH. Detection of Kawasaki disease-associated antigen in inflamed gastrointestinal tract in acute Kawasaki disease. Pediatr Infect Dis J 2005;24:927-929.
  • Miura M, Ohki H, Yoshiba S, Ueda H, Sugaya A, Satoh M, Yamagishi H. 2005. Adverse effects of methylprednisolone pulse therapy in refractory Kawasaki disease. Arch Dis Child, 90:1096-1097.
  • Morii T, Ohno Y, Hirose H, Kawabe H, Ogata T, Hirano K, Eguchi T, Maruyama T, Kanno Y, Hayashi M, Saito I, Saruta T. 2005. Cellular insulin resistance in Ebstein-Barr virus-transformed lymphoblasts from young insulin-resistant Japanese men. Metabolism, 54:370-375.
  • Morleo M, Pramparo T, Perone L, Gregato G, C LC, Mueller R, Ogata T, Raas-Rothshild A, M CdB, Wilson L, Zaidman G, Zuffardi O, Ballabio A, Franco B. 2005. Microphthalmia with linear skin lesions (MLS) syndrome: clinical, cytogenetic and molecular characterization of 11 cases and mutation analysis of candidate genes in karyotypically normal cases. Am J Med Genet, 137A:190-198.
  • Motoyama O, Hasegawa A, Honda M. 2005. A prospective trial of steroid withdrawal after renal transplantation treated with cyclosporine and mizoribine in children. Results obtained between 1990 and 2003. Pediatr Transplant, 9:232-238.
  • Munkanta M, Terunuma H, Takahashi M, Hanabusa H, Miura T, Ikeda S, Sakai M, Fujii T, Takahashi Y, Oka S, Matsuda J, Ishikawa M, Taki M, Takashima Y, Mimaya J, Ito M, Kimura A, Yasunami M. HLA-B polymorphism in Japanese HIV-1-infected long-term surviving hemophiliacs. Viral Immunol 2005;18:500-505.
  • Murakami N, Sakuta R, Takahashi E, Katada Y, Nagai T, Owada M, Nishino I, Nonaka I. Early onset distal muscular dystrophy with normal dysferlin expression. Am J Med Genet 2005;136:45-48.
  • Nagao K, Ota T, Tanikawa A, Takae Y, Mori T, Udagawa S, Nishikawa T. 2005. Genetic identification and detection of human pathogenic Rhizopus species, a major mucormycosis agent, by multiplex PCR based on internal transcribed spacer region of rRNA gene. J Dermatol Sci, 39:23-31.
  • Naito YY, Hida M, Maruyama Y, Hori N, Awazu M. 2005. Poststreptococcal acute glomerulonephritis superimposed on bilateral renal hypoplasia. Clin Nephrol, 63:477-480.
  • Nakashima E, Kitoh H, Maeda K, Haga N, Kosaki R, Mabuchi A, Nishimura G, Ohashi H, Ikegawa S. 2005. Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia. Am J Med Genet, 132:A:181-4.
  • Narumi S, Hasegawa T, Shimada H, Shimasaki N, Takahashi T, Mori T. Growth-chart-based qualitative evaluation for height growth after hematopoietic stem cell transplantation. Pediatric Transplantation 2005;10:26-31.
  • Nozu K, Iijima K, Sakaeda T, Okumura K, Nakanishi K, Yoshikawa N, Honda M, Ikeda M, Matsuo M. 2005. Cyclosporin A absorption profiles in children with nephrotic syndrome. Pediatr Nephrol, 20:910-913.
  • Ogata T, Fukami M. Clinical lessons from SHOX mutation research. Int Growth Monitor (in press).
  • Ogata T, Yoshida R. 2005. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes. Pediatr Endocrinol Rev, 2:669-674.
  • Rowley AH, Shulman ST, Garcia FL, Guzman-Cottrill JA, Miura M, Lee HL, Baker SC. Cloning the arterial IgA antibody response during acute Kawasaki disease. J Immunol 2005;175:8386-8391.
  • Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N. 2005. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephritic syndrome. Kidney Int, 67:1248-1255.
  • Sato N, Hasegawa T, Hori N, Fukami M, Yoshimura Y, Ogata T. 2005. Gonadotropin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families. Hum Reprod, 20:2173-2178.
  • Shen J, Eyaid W, Mochida GH, Al-Moayyad F, Bodell A, Woods CG, Walsh CA. ASPM mutations identified in patients with primary microcephaly and seizures. J Med Genet 2005;42:725-729.
  • Shimada H, Shima H, Shimasaki N, Yoshihara H, Mori T, Takahashi T. 2005. Little response to zoledronic acid in a child of juvenile myelomonocytic leukemia (JMML) harboring the PTPN11 mutation. Ann Oncol, 16:1400.
  • Shimasaki N, Shimada H, Ando Y, Mori T. 2005. Anterior chamber involvement in MLL-AF9 fusion gene leukemia. BloodMed.com;(Web Journal).
  • Shinjoh M, Miyairi I, Sakurai M, Takahashi M, Ariyasu D, Nakayama T, Tokumura M, Yamashita R, Sunakawa K, Takahashi T. 2005. Cryptococcal meningitis in an immunocompetent child. Eur J Pediatr, 164:596-7.
  • Soneda S, Fukami M, Matsuo N, Hasegawa T, Fujimoto M, Koitabashi Y, Ogata T. 2005. Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling. Endocr J, 52:83-88.
  • Sugaya N, Takeuchi Y. Mass vaccination of schoolchildren against influenza and its impact on the influenza-associated mortality rate among children in Japan . Clin Infect Dis 2005;41:939-947.
  • Tanigaki S, Miyakoshi K, Tanaka M, Hattori Y, Matsumoto T, Ueno K, Uehara K, Nishimura O, Minegishi K, Ishimoto H, Shinmoto H, Ikeda K, Yoshimura Y. 2005. Pulmonary hypoplasia: prediction with use of ratio of MR imaging-measured fetal lung volume to US-estimated fetal body weight. Radiology, 232:767-72.
  • Tarui T, Takahashi T, Nowakowski RS, Hayes NL, Bhide PG, Caviness VS. 2005. Overexpression of p27 Kip 1, probability of cell cycle exit, and laminar destination of neocortical neurons. Cereb Cortex, 15:1343-55.
  • Tsuji A, Araki K, Maeyama K, Hashimoto K. Effectiveness of Oral Magnesium in a Ptient With Ventricular Tachycardia Due to Hypomagnesemia. J Cardiovasc Pharmacol Therapeut 2005;10:205-208.
  • Udaka T, Samejima H, Kosaki R, Kurosawa K, Okamoto N, Mizuno S, Makita Y, Numabe H, Toral J, Takahashi T, Kosaki K. Comprehensive screening of CREBBP mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography. Congenit Anom 2005;45:125-131.
  • Udaka T, Torii C, Takahashi D, Mori T, Aramaki M, Kosaki R, Tanigawara Y, Takahashi T, Kosaki K. 2005. Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography. Genet Test, 9:85-92.
  • Ushio M, Yui I, Yoshida N, Fujino M, Yonekawa T, Ota Y, Notomi T, Nakayama T. Detection of respiratory syncytial virus genome by subgroups-A, B specific reverse transcription loop-mediated isothermal amplification (RT-LAMP). J Med Virol 2005;77:121-127.
  • Wada Y, Okada M, Fukami M, Hasegawa T, Sasagawa I, Ogata T. Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1. Fertil Steril (in press).
  • Wada Y, Okada M, Hasegawa T, Ogata T. 2005. Association of severe micropenis with Gly146Ala polymorphism in the gene for steroidogenic factor-1. Endocr J;52:445-448.
  • Yoshida R, Fukami M, Sasagawa I, Hasegawa T, Kamatani N, Ogata T. 2005. Association of cryptorchidism with a specific haplotype of the estrogen receptor a gene: implication for the susceptibility to estrogenic environmental endocrine disruptors. J Clin Endocrinol Metab, 90:4716-4721.