Publications 2009

  • Adachi M, Muroya K, Asakura Y, Kondoh Y, Ishihara J, Hasegawa T. Ectopic calcification as discernible manifestation in neonates with pseudohypoparathyroidism type 1a. International J Endocrinol 2009; 931057 Epub, 2009 (Online journal).
  • Arai F, Yoshihara H, Hosokawa K, Nakamura Y, Gomei Y, Iwasaki H, Suda T. Niche regulation of hematopoietic stem cells in the endosteum. Ann N Y Acad Sci. 2009;1176:36-46.
  • Aso K, Izawa M, Higuchi A, Kotoh S, Hasegawa Y.　Stress Doses of Glucocorticoids Cannot Prevant Progression of All Adrenal Crises．Clin Pediatr Endocrinol 2009;18: 23-27.
  • Chiba N, Murayama SY, Morozumi M, Nakayama E, Okada T, Iwata S, Sunakawa K, Ubukata K.: Rapid detection of eight causative pathogens for the diagnosis of bacterial meningitis by real-time PCR. J Infect Chemother. 2009; 15: 92-98.
  • Dateki S, Hizukuri K, Tanaka T, Katsumata N, Yokoya S, Katavetin P, Ogata T. An immunologically anomalous but considerably bioactive growth hormone produced by a novel GH1 mutation (p.D116E). Eur J Endocrinol 2009;161: 301–306.
  • Dong J-B, Saito A, Mine Y, Sakurabe Y, Nibe K, Goto Y, Komase K, Nakayama T, Miyata H, Iwata H, Haga T. Adaptation of wild-type measles virus to cotton rat lung cells: E89K mutation in matrix protein contributes to its fitness. Virus Gene 2009;39:330-334.
  • Fujisaki H, Kakuda H, Shimasaki N, Imai C, Ma J, Lockey T, Eldridge P, Leung WH, Campana D. Expansion of highly cytotoxic human natural killer cells for cancer cell therapy. Cancer Res. 2009;69:4010-7.
  • Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T. Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients. J Clin Endocrinol Metab 2009;94: 1723-1731.　
  • Fukushi D, Watanabe N, Kasai F, Haruta M, Kikuchi A, Kikuta A, Kato K, Nakadate H, Tsunematsu Y, Kaneko Y. Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification, in neuroblastoma tumors. Cancer Genet Cytogenet. 2009;188:32-41.
  • Furukawa S, Haruta M, Arai Y, Honda S, Ohshima J, Sugawara W, Kageyama Y, Higashi Y, Nishida K, Tsunematsu Y, Nakadate H, Ishii M, Kaneko Y. Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes. Cancer Sci. 2009 ;100:698-708.
  • Hamano-Hasegawa K, Morozumi M, Nakayama E, Chiba N, Murayama SY, Takayanagi R, Iwata S, Sunakawa K, Ubukata K.; Acute Respiratory Diseases Study Group.: Comprehensive detection of causative pathogens using real-time PCR to diagnose pediatric community-acquired pneumonia. J Infect Chemother. 2009; 14: 424-432.
  • Hamasaki Y, Yoshikawa N, Hattori S, Sasaki S, Iijima K, Nakanishi K, Matsuyama T, Ishikura K, Yata N, Kaneko T, Honda M. Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome. Pediatr Nephrol. 2009;24:2177-2185.
  • Hattori M, Torii C, Yagihashi T, Izumi K, Suda N, Ohyama K, Takahashi T, Moriyama K, Kosaki K. Diagnosis of Russell-Silver Syndrome by the combined bisulfite restriction analysis – Denaturing high-performance liquid chromatography assay. Genet Test Mol Biomarkers 2009;13:623-30.
  • Hayakawa K, Katsumata N, Abe K, Hirano M, Yoshikawa K, Ogata T, Horikawa R, Nagamine T. Wide range of biotin (vitamin H) content in the foodstuffs and powdered milks assessed by the high-performance affinity chromatography. Clin Pediatr Endocrinol 2009 18: 41–49.
  • Hilton E, Johnston J, Whalen S, Okamoto N, Hatsukawa Y, Nishio J, Kohara H, Hirano Y, Mizuno S, Torii C, Kosaki K, Manouvrier S, Boute O, Perveen R, Law C, Moore A, Fitzpatrick D, Lemke J, Fellmann F, Debray FG, Dastot-Le-Moal F, Gerard M, Martin J, Bitoun P, Goossens M, Verloes A, Schinzel A, Bartholdi D, Bardakjian T, Hay B, Jenny K, Johnston K, Lyons M, Belmont JW, Biesecker LG, Giurgea I, Black G. BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects. Eur J Hum Genet 2009;17:1325-35.
  • Homma K, Hida M, Ikeda K, Yamaga N, Murata M, Hasegawa T. The measurement of serum 17a-hydroxyprogesterone in newborn infants by stable isotope dilution – gas chromatography / mass spectrometry. Clin Pediatr Endocrinol 2009;18: 77-80.
  • Horiuchi Y, Onodera M, Miyagawa Y, Sato B, Onda K, Katagiri U, Okita H, Okada M, Otsu M, Kume A, Okuyama T, Fujimoto J, Kuratsuji T, Kiyokawa N. Kinetics and Effect of Integrin Expression on Human CD34(+) Cells during Murine Leukemia Virus-Derived Retroviral Transduction with Recombinant Fibronectin for Stem Cell Gene Therapy. Hum Gene Ther. 2009; 20: 777-783.
  • Horiuchi Y, Onodera M, Miyagawa Y, Sato B, Onda K, Katagiri YU, Okita H, Okada M, Otsu M, Kume A, Okuyama T, Fujimoto J, Kuratsuji T, Kiyokawa N. Kinetics and Effect of Integrin Expression on Human CD34(+) Cells during Murine Leukemia Virus-Derived Retroviral Transduction with Recombinant Fibronectin for Stem Cell Gene Therapy. Hum Gene Ther 2009;20:777-83.
  • Hosoki K, Kagami M, Tanaka T, Kubota M, Kurosawa K, Kato M, Uetake K, Tohyama J, Ogata T, Saitoh S. Maternal uniparental disomy 14 syndrome demonstrates Prader-Willi syndrome-like phenotype. J Pediatr 2009;155: 900-903.
  • Imashuku S, Kinugawa N, Matsuzaki A, Kitoh T, Ohki K, Shioda Y, Tsunematsu Y, Imamura T, Morimoto A; Japan LCH Study Group. Langerhans cell histiocytosis with multifocal bone lesions: comparative clinical features between single and multi-systems. Int J Hematol 2009;90:506-12.
  • Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Official Japanese reports significantly underestimate prevalence of overweight in school children : Inappropriate definition of standard weight and calculation of excess weight. Ann Hum Biol 2009;36: 139-145.
  • Jongmans MC, van Ravenswaaij-Arts CM, Pitteloud N, Ogata T, Sato N, Claahsen-van der Grinten HL, van der Donk K, Seminara S, Bergman JE, Brunner HG, Crowley WF Jr, Hoefsloot LH. CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome. Clin Genet 2009;75: 65–71.
  • Kasahara M, Horikawa R, Sakamoto S, Shigeta T, Tanaka H, Fukuda A, Abe K, Yoshii K, Naiki Y, Kosaki R, Nakagawa A. Living donor liver transplantation for glycogen storage disease type Ib. Liver Transpl. 2009;15:1867-71.
  • Kashima K, Takakuwa K, Suzuki M, Makino M, Kaneko S, Kato S, Hanabusa H, Tanaka K. Studies of assisted reproduction techniques (ART) for HIV-1-discordant couples using washed sperm and the nested PCR method: a comparison of the pregnancy rates in hiv-1-discordant couples and control couples. Jpn J Infect Dis. 2009;62:173-6.
  • Kinai E, Hanabusa H. Progressive renal tubular dysfunction associated with long-term use of Tenofovir DF. AIDS Res Hum Retroviruses 2009 ;25: 387-394
  • Kobayashi H, Yamada K, Morita S, Hiura H, Fukuda A, Kagami M, Ogata T, Hata K, Sotomaru Y, Kono T. Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. Genomics 2009;93:461–472.
  • Kodo K, Nishizawa T, Furutani M, Arai S, Yamamura E, Joo K, Takahashi T, Matsuoka R, Yamagishi H. GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling. Proc Natl Acad Sci U S A. 2009;106:13933-13938.
  • Kumamoto S, Katafuchi T, Nakamura K, Endo F, Oda E, Okuyama T, Kroos MA, Reuser AJ, Okumiya T.High frequency of acid alpha-glucosidase pseudodeficiency complicates newborn screening for glycogen storage disease type II in the Japanese population. Mol Genet Metab 2009; 97:190-195.
  • Matsubara K, Morozumi M, Okada T, Matsushima T, Komiyama O, Shoji M, Ebihara T, Ubukata K, Sato Y, Akita H, Sunakawa K, Iwata S. A comparative clinical study of macrolide-sensitive and macrolide-resistant Mycoplasma pneumoniae infections in pediatric patients. J Infect Chemother 2009;15:380-383.
  • Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet 2009;46(4):242-8.
  • Mitsuhashi T, Takahashi T. Cell cycle. In Encyclopedia of Neuroscience. Binder MD, Hirokawa N, Windhorst U, Hirsch MC (eds), Murakami F (section ed). Springer-Verlag, Berlin, 2009.
  • Mitsuhashi T, Takahashi T. Genetic regulation of proliferation/differentiation characteristics of neural progenitor cells in the developing neocortex. Brain Dev 2009;31(7):553-7.
  • Mitsui T, Mori T, Fujita N, Inada H, Horibe K, Tsurusawa M; Lymphoma Committee, Japanese Pediatric Leukemia/Lymphoma Study Group. Retrospective analysis of relapsed or primary refractory childhood lymphoblastic lymphoma in Japan. Pediatr Blood Cancer. 2009;52:591-5.
  • Miwa M, Kusuda S, Ikeda K. Late-onset Circulatory Collapse in Very Low-birthweight Infants: A Japanese Perspective. NeoReviews 2009;10;e381-e386
  • Miyazaki O, Nishimura G, Okamoto R, Masaki H, Kumagai M, Shioda Y, Nozawa K, Kitoh H. Induction of systemic bone changes by preconditioning total body irradiation for bone marrow transplantation. Pediatr Radiol. 2009;3923-9.
  • Miyoshi Y, Oue T, Oowari M, Soh H, Tachibana M, Kimura S, Kiyohara Y, Yamada H, Bessyo K, Mushiake S, Homma K, Hasegawa T, Sasano H, Ozono K. A case of pediatric virilizing adrenocortical tumor resulting in hypothalamic-pituitary activation and central precocious puberty following surgical removal. Endocr 2009;J 56: 975-982.
  • Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA. A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly. Am J Hum Genet 2009;85:897-902.
  • Mochida GH. Genetics and biology of microcephaly and lissencephaly. Semin Pediatr Neurol 2009 ;16:120-6.
  • Murayama SY, Seki C, Sakata H, Sunaoshi K, Nakayama E, Iwata S, Sunakawa K, Ubukata K; the Invasive Streptococcal Disease Working Group.: Capsular type and antibiotic resistance in Streptococcus agalactiae isolates from patients with invasive infections, ranging from newborns to the elderly. Antimicrob Agents Chemother. 2009; 53: 2650-2653.
  • Nagai M, Ji YX, Yoshida N, Miyata A, Fujino M, Ihara T, Yoshikawa T,  Asano Y, Nakayama T. Modified adult measles in outbreaks in Japan, 2007-08. J Med Virol. 2009; 81: 1094-1101.
  • Naito Y, Kimura T, Aramaki M, Izumi K, Okada Y, Suzuki H, Takahashi T, Kosaki K. Caudal regression and tracheoesophageal malformation induced by adriamycin: A novel chick model of VATER association.  Pediatr Res, 2009; 65:607-12.
  • Nakanishi K, Iijima K, Ishikura K, Hataya H, Awazu M, Sako M, Honda M, Yoshikawa N, for the Japanese Pediatric IgA Nephropathy Treatment Study Group. Efficacy and safety of lisinopril for mild childhood IgA nephropathy: a prospective single-arm trial. Pediatr Nephrol. 24:845-849, 2009
  • Narumi S, Muroya K, Abe Y, Yasui M, Asakura Y, Adachi M, Hasegawa T. TSHR mutations as a cause of congenital hypothyroidism in Japan: a population-based genetic study. J Clin Endocrinol Metab 2009;94: 1317-1323.
  • Ogata T, Laporte J, Fukami M. MAMLD1 (CXorf6): a new gene involved in hypospadias. Hor Res 2009;71: 245–252.
  • Richard SA, Sugaya N, Simonsen L, Miller MA, Viboud C.A comparative study of the 1918-1920 influenza pandemic in Japan, USA and UK: mortality impact and implications for pandemic planning. Epidemiol Infect. 2009;137: 1062-1072.
  • Rotenberg A, Bae EH, Takeoka M, Tormos JM, Schachter SC, Pascual-Leone A. Repetitive transcranial magnetic stimulation in the treatment of epilepsia partialis continua. Epilepsy Behav 2009;14(1):253-7.
  • Sakata M, Komase K, Nakayama T. Histidine at position 1042 of the p150 region of a KRT live attenuated rubella vaccine strain is responsible for the temperature sensitivity. Vaccine 2009; 27: 234-242.
  • Sato T, Onai N, Yoshihara H, Arai F, Suda T, Ohteki T. IRF-2 protects quiescent HSCs from type-I interferon-dependent exhaustion. Nature Medicine 2009;15:696-700.
  • Shima H, Inokuchi M, Shimada H. A case of multisystem Langerhans cell histiocytosis with primary hypothyroidism followed by type 1 diabetes mellitus. Pediatr Blood Cancer. 2009;53:232-4.
  • Shima H, Takubo K, Iwasaki H, Yoshihara H, Gomei Y, Hosokawa K, Arai F, Takahashi T, Suda T. Reconstitution activity of hypoxic cultured human cord blood CD34-positive cells in NOG mice. Biochem Biophys Res Commun 2009; 378:467-72.
  • Shinjoh M, Takahashi T. Varicella zoster exposure on paediatric wards between 2000 and 2007: safe and effective post-exposure prophylaxis with oral aciclovir. J Hosp Infect. 2009; 72: 163-168.
  • Sim SC, W Miller WL, Zhong X-B, Arlt W, Ogata T, Ding X, Wolf R, Fluck CE, Pandey AV, Henderson CJ, Porter TD, Daly AK, Nebert DW, Ingelman-Sundberg M. Nomenclature for alleles of the cytochrome P450 oxidoreductase (POR) gene. Phamacogenet Genomics 2009;19 : 565–566.
  • Suda K, Kudo Y, Higaki T, Nomura Y, Miura M, Matsumura M, Ayusawa M, Ogawa S, Matsuishi T. Multicenter and retrospective case study of warfarin and aspirin combination therapy in patients with giant coronary aneurysms caused by Kawasaki disease. Circulation Journal 2009 73:1319-1323
  • Sugawa F, Wada Y, Okada M, Maruyama T, Uchida H, Arase T, Hamada N, Ishizuka B, Ogata T. Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns. Fertil Steril 2009;91:649–652.
  • Tamura D, Mitamura K, Yamazaki M, Fujino M, Nirasawa M, Kimura K, Kiso M, Shimizu H, Kawakami C, Hiroi S, Takahashi K, Hata M, Minagawa H, Kimura Y, Kaneda S, Sugita S, Horimoto T, Sugaya N, Kawaoka Y. Oseltamivir-resistant influenza a viruses circulating in Japan. J Clin Microbiol. 2009; 47: 1424-1427.
  • Thibert RL, Burns JD, Bhadelia R, Takeoka M. Reversible uncal herniation in a neonate with a large MCA infarct. Brain Dev 2009;31:763-5.
  • Treviño LR, Shimasaki N, Yang W, Panetta JC, Cheng C, Pei D, Chan D, Sparreboom A, Giacomini KM, Pui CH, Evans WE, Relling MV. Germline genetic variation in an organic anion transporter polypeptide associated with methotrexate pharmacokinetics and clinical effects. J Clin Oncol 2009;27:5972-8.
  • Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T. Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia or acampomelic campomelic dysplasia. Am J Med Genet 2009;149A: 2882-2885.
  • Watanabe H. Akachan ni Kanpai ! Celebrating the Baby: Baby, Family, Culture. Journal of Infant Mental Health 2009 (in press)
  • Yagihashi T, Asada H, Furuya M, Kosaki K, Takahashi T, Yoshimura Y. Association between patient age at the time of surgical treatment for endometriosis and aryl hydrocarbon receptor repressor polymorphism. Fertil Steril 2009;92:1240-1242.
  • Yagihashi T, Mizuno M,  Chino B,  Sato Y,  Sakuma K,  Takebayashi T, Takahashi T, Kosaki K. Effects of the CYP2D6*10 alleles and co-medication with CYP2D6-dependent drugs on risperidone metabolism in patients with schizophrenia.  Hum Psychopharmacol. 2009; 24:301-8.
  • Yamagishi H and Fukuda K. Truncus arteriosus. Encyclopedia of Molecular Mechanisms of Disease 2009 (in press)
  • Yamagishi H, Maeda J, Uchida K, Tsuchihashi T, Nakazawa M, Aramaki M, Kodo K, Yamagishi C. Molecular embryology for an understanding of congenital heart diseases. Anatomical Science International 2009 84: 88-94
  • Yamaguchi K, Hisano M, Irie S, Arata N, Watanabe N, Kubo T, Kato T, Murashima A.　 Relationship of Th1/Th2 Cell Balance With the Immune Response to Influenza Vaccine During Pregnancy. J Med Virol 2009;81:1923-1928.
  • Yamaguchi Y, Hanaki H, Yanagisawa C, Ikeda-Dantsuji Y, Hashimoto T, Yazaki H, Sugahara K, Yanagisawa T, Kawajiri H, Sato S, Is２hizaki A, Tachihara-Sato R, Takahashi Y, Ono T, Kageyama Y, Kawaguchi T, Tamura A, Hagane K, Sunakawa K. Characterization of beta-lactam antibiotic-induced vancomycin-resistant MRSA (BIVR) in a patient with septicemia during long-term vancomycin administration. J Infect Chemother2009;15:274-278.
  • Yap V, Engel M, Takenouchi T, Perlman JM. Seizures are common in term infants undergoing head cooling. Pediatr Neurol 2009;41:327-31.