研究業績

Publications 2007

  • Aramaki M, Kimura T, Udaka T, Kosaki R, Mitsuhashi T, Okada Y, Takahashi T, Kosaki K. Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome. Birth Defects Res A Clin Mol Teratol, 2007; 79:50-57.
  • Aramaki M, Udaka T, Torii C, Samejima H, Kosaki R, Takahashi T, Kosaki K. Comprehensive screening of CHD7 mutations among patients with CHARGE Syndrome using denaturing high-performance liquid chromatography, Genet Test, 2006; 10:244-251.
  • Awazu M. Epidemiology of hypertension. Pediatric Nephrology 6th edition. Avner, Harmon, Niaudet, Yoshikawa, eds. Lippincott Williamas & Wilkins (in press).
  • Barada K, Hanaki H, Ikeda S, Yamaguch Y, Akama H, Nakae T, Inamatsu T and Sunakawa K: Trends in the gentamicin and arbekacin susceptibility of methicillin-resistant Staphylococcus aureus and the genes encoding aminoglycoside-modifying enzymes . J Infect. Chemother 2007; 13;74-78.
  • Batista CM, Kippin TE, Willaime-Morawek S, Shimabukuro KM, Akamatsu W, van der Kooy D. A Progressive and Cell Non-Autonomous Increase in Striatal Neural Stem Cells in the Huntington's Disease R6/2 Mouse. J.Neurosci 2006;26:10452-60.
  • Fujino M, Yoshida N, Kimura K, Zhou J, Motegi Y, Komase K, Nakayama T. Development of a new neutralization test for measles virus. J Virol Meth 2007; 142: 15-20.
  • Fujita H, Samejima H, Kitagawa N, Mitsuhashi T, Washio T, Yonemoto J, Tomita M, Takahashi T, Kosaki K. Genome-wide screening of dioxin-responsive genes in fetal brain: bioinformatic and experimental approaches. Congenit Anomal, 2006; 46:135-143.
  • Fukami M, Wada Y, Miyabayashi K, Nishino I, Hasegawa T, Camerino G, Kretz C, Buj-Bello A, Laporte J, Yamada G, Morohashi K, Ogata T. CXorf6 is a novel causative gene for hypospadias. Nat Genet 2006;38:1369-1371.
  • Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J.Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis. J Hum Genet 2007;52:397-405.
  • Honda S, Hayashi S, Kato M, Niida Y, Hayasaka K, Okuyama T, Imoto I, Mizutani S, Inazawa J. Clinical and molecular cytogenetic characterization of two patients with non-mutational aberrations of the FMR2 gene. Am J Med Genet 2007, 143:687-93.
  • Hosoi H, Teramukai S, Matsumoto Y, Tsuchiya K, Iehara T, Hara J, Mitsui T, Kaneko M, Hatae Y, Hayashi Y, Mabuchi O, Adachi N, Morikawa Y, Nishimura S, Kumagai M, Takamatsu H, Sawada T, Sugimoto T. A review of 331 rhabdomyosarcoma cases in patients treated between 1991 and 2002 in Japan. Int J Clin Oncol. 2007;12:137-45.
  • Hanaki H, Hososaka Y, Yanagisawa C, Otsuka Y, Nagasawa Z, Nakae T and Sunakawa K: Occurrence of vancomycin-intermediate-resistant Staphylococcus aureus in Japan. J Infect. Chemother 2007; 13: 118-121
  • Hasegawa K, Kobayashi R, Nakayama E, Takada E, Ono A, Chiba N, Morozumi M, Iwata S, Sunakawa K, Ubukata K;High prevalence of type b b-lactamase-nonproducing ampicillin-resistant Haemophilus influenzae in meningitis: the situation in Japan where Hib vaccine has not been introduced J Antimicrob Chemother 2006; 57:1077-1082.
  • Hososaka Y, Hanaki H, Endo H, Suzuki Y, Nagasawa Z, Otsuka Y, Nakae T and Sunakawa K; Characterization of oxacillin-susceptible mecA -positive Staphylococcus aureus : a new type of MRSA. J Infect. Chemother. 2007; 13; 79-86.
  • Hachiya R, Ohashi Y, Kamei Y, Suganami T, Mochizuki H, Mitsui N, Sakuragi M, Nishimura G, Ohashi H, Hasegawa T, Ogawa Y. Intact kinase homology domain of natriuretic peptide receptor-B is essential for skeletal development. J Clin Endocrinol Metab (in press).
  • Hayakawa K, Guo L, Terentyeva EA, Li XK, Kimura H, Hirano M, Yoshikawa K, Nagamine T, Katsumata N, Ogata T, Tanaka T. Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota). J Chromatogr B Analyt Technol Biomed Life Sci 2006;844:240-250.
  • Hatakeyama S, Sugaya N, Ito M, Yamazaki M, Ichikawa M, Kimura K, Kiso, M. Shimizu, H. Kawakami, C. Koike, K. Mitamura, K. Kawaoka, Y. Emergence of influenza B viruses with reduced sensitivity to neuraminidase inhibitors. JAMA. 2007;29:1435-42.
  • Hirose Y, Nakashima E, Ohashi H, Mochizuki H, Bando Y, Ogata T, Adachi M, Toba E, Nishimura G, Ikegawa S. Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia. J Hum Genet 2006;51:706-710.
  • Homma K, Sato A, Watanabe H, Hasegawa T. The circadian variation of cortisol secretion in patients with anorexia nervosa in childhood and adolescence after recovery of body weight by treatment using GC/MS (gas chromatography / mass spectrometry) in SIM (selected ion monitoring). Cin Pediatr Endocrinol 2007;16:17-22.
  • Inokuchi M, Hasegawa T, Anzo M, Matsuo N. Standardized Centile Curves of Body Mass Index for Japanese Children and Adolescents Based on the 1978-1981 National Survey Data. Ann Hum Biol 2006;33:444-453.
  • Inokuchi M, Matsuo N, Anzo M, Takayama JI, Hasegawa T. Age dependent percentile for waist circumference for Japanese children based on the 1992-1994 cross-sectional national survey data. Eur J Pediatr 2007;166:655-651.
  • Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Prevalence and trends of underweight and BMI distribution changes in Japanese teenagers based on the 2001 National Survey data. Ann Hum Biol 2007;34:354-361.
  • Inokuchi M, Matsuo N, Anzo M, Hasegawa T. Body mass index reference values (mean and SD) for Japanese children. Acta Paediatr (in press).
  • Izumi K, Aramaki M, Kimura T, Naito Y, Udaka T, Uchikawa M, Kondoh H, Suzuki H, Cho G, Okada Y, Takahashi T, Golden JA, Kosaki K Identification of a prosencephalic-specific enhancer of SALL1: Comparative genomic approach using the chick embryo. Pediatr Res, 61:660-665.
  • Izumi K, Jones KL, Kosaki K, Benirschke K. Umbilical cord length in urinary tract abnormalities associated with oligohydramnios: Evidence regarding developmental pathogenesis. Fetal Pediatr Pathol, 2006; 25:233-240.
  • Izumi K, Kohta T, Kimura Y, Takahashi T, Ishiko A, Kosaki K. Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal, Clin Genet (in press).
  • Izumi K, Kuratsuji G, Ikeda K, Takahashi T, Kosaki K. Partial deletion of LIS1: A pitfall in molecular diagnosis of Miller-Dieker syndrome. Pediatr Neurol, 2007; 36:258-260.
  • Izumi K, Nakano M, Kosaki K, Kosaki R, Hosokai N, Matsumoto H, Hasegawa T, Takahashi T, Kosaki K. Two distinctive mechanisms leading to disruption of the SHOX transcription unit in a single family. Am J Med Genet (in press).
  • Kanemoto K, Ishikura K, Ariyasu D, Hamasaki Y, Hataya H, Hasegawa Y, Ikeda M.
  • WT1 intron 9 splice acceptor site mutation in a 46, XY male with focal segmental glomerulosclerosis. Pediatr Nephrol, 2007;22:454-458.
  • Kagami M, Nagai T, Fukami M, Yamazawa K, Ogata T. Silver-Russell syndrome in a girl bornafter in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST. J Assist Reprod Genet 2007;24:131-136.
  • Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC,
  • Ishino F, Ogata T. Deletions and epimutations affecting the human chromosome 14q32.2 imprinted region: implications for the development of paternal and maternal upd(14)-like phenotypes. Nat Genet (in press).
  • Kanno J, Kure S, Narisawa A, Kamada F, Takayanagi M, Yamamoto K, Hoshino H, Goto T, Takahashi T, Haginoya K, Tsuchiya S, Baumaister FAM, Aoki Y, Matsubara Y. Allelic and non-allelic heterogeneities in pyridoxine-dependent seizures by mutational analysis of ALDH7A1 gene. Mol Genet Metab 2007;91:384-389.
  • Kawana A, Teruya K, Kirikae T, Sekiguchi J, Kato T, Kuratsuji T et al. "Syndromic surveillance within a hospital" for early detection of a nosocomial outbreak of acute respiratory infection. Jpn J Infect Dis 2006; 59: 377-379.
  • Kimura R, Takeshima K, Mizuno S, Kosaki K, Machida J, Kamamoto M, Muro Y, Shimosato K, Wakamatsu N, Sonta S, Ono T. Monopolar preparation of human lymphocytes for evaluation of the metaphase chromosome alignment. Chromosome Sci 9: 75-83, 2006.
  • Kitamura A, Tsukaguchi H, Iijima K, Araki J, Hattori M, Ikeda M, Honda M, Nozu K, Nakazato H, Yoshikawa N, Kagami S, Muramatsu M, Choi Y, Cheong HI, Doi T. Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome. Nephrol Dial Transplant. 2006 21:3133-3138.
  • Kobayashi S, Murayama S, Tatsuzawa O, Koinuma G, Kawasaki K, Kiyotani C, Kumagai M. X-linked severe combined immunodeficiency (X-SCID) with high blood levels of immunoglobulins and Aspergillus pneumonia successfully treated with micafangin followed by unrelated cord blood stem cell transplantation. Eur J Pediatr. 2007;166:207-10.
  • Kobayashi Y, Hasegawa O, Honda M. Terminal complement complexes in childhood type I membranoproliferative glomerulonephritis. J Nephrol, 2006;19:746-750.
  • Kinai E, Hanabusa H, Kato S. Prediction of the efficacy of antiviral therapy for hepatitis C virus infection by an ultrasensitive RT-PCR assay. J Med Virol. 2007;79:1113-9.
  • Konno M, Baba S, Mikawa H, Hara K, Matsumoto F, Kaga K, Nishimura T, Kobayashi T, Furuya N, Moriyama H, Okamoto Y, Furukawa M, Yamanaka N, Matsushima T, Yoshizawa Y, Kohno S, Kobayashi K, Morikawa A, Koizumi S, Sunakawa K, Inoue M, Ubukata K. Study of nasopharyngeal bacterial flora: Secpnd report. Variations in nasopharyngeal bacterial flora in children aged 6 years or younger when administered antimicrobial agents. Part 1. J Infect Chemother .2006; 12: 287-304.
  • Konno M, Baba S, Mikawa H, Hara K, Matsumoto F, Kaga K, Nishimura N, Kobayashi K, Furuya N, Moriyama H, Okamoto Y, Furukawa M , Yamanaka N, Matsushima T, Yoshizawa Y, Kohno S, Kobayashi K, Morikawa S, Koizumi S, Sunakawa K, Inoue M, Ubukata K; Study of nasopharyngeal bacterial flora. Second report. Variations in nasopharyngeal bacterial flora in children aged 6 years or younger when administered antimicrobial agents. Part 2. J Infect Chemother 2006; 12: 305-30.
  • Kosaki R, Fujimaru R, Samejima H, Yamada H, Izumi K, Iijima K, Kosaki K. Wide phenotypic variations within a family with SALL1 mutations: Isolated external ear abnormalities to Goldenhar syndrome. Am J Med Genet, 2007; 143: 1087-90.
  • Kosaki R, Okuyama T, Tanaka T, Migita O, Kosaki K. Monozygotic twins of Smith-Magenis syndrome. Am J Med Genet, 2007; 143:768-769.
  • Kosho T, Sakazume S, Kawame H, Wakui K, Wada T, Okoshi Y, Mikawa M, Hasegawa T, Matsuura N, Niikawa N, Matsumoto N, Fukushima Y. De novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment. Clin Dysmorphol (in press).
  • Kuroda T, Saeki M, Honna T, Kumagai M, Masaki H. Late complications after surgery in patients with neuroblastoma. J Pediatr Surg. 2006;41:2037-40.
  • Matsunaga T, Okada M, Usami S, Okuyama T. Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1. Acta Otolaryngol 2007, 127:98-104.
  • Maesaka A, Higuchi A, Kotoh S, Hasaegawa Y, Ikeda M, Shishido S, Honda M. Gonadal function in 15 patients associated with WT1 gene mutations. Clin Pediatr Endocrinol, 2006;15:143-149.
  • 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 (in press).
  • Miyairi I, Tatireddigari VR, Mahdi OS, Rose LA, Belland RJ, Lu L, Williams RW, Byrne GI. The p47 GTPases Iigp2 and Irgb10 regulate innate immunity and inflammation to murine Chlamydia psittaci infection. J Immunol. 2007;179:1814-1824.
  • Miyamoto J, Asanuma H, Nakai H, Hasegawa T, Nawata H, Hasegawa Y. Mutational analysis of androgen receptor genes (AR) in 46,XY patients with ambiguous genitalia and normal testosterone secretion: Endocrinological characteristics of three patients with AR gene mutations. Clin Pediatr Endocrinol 2006;15:151-162.
  • Mori N, Motegi Y, Shimamura Y, Ezaki T, Natsumeda T, Yonekawa T, Ota Y, Notomi T, Nakayama T. Development of a new method for diagnosis of rubella virus infection by reverse transcription-loop mediated isothermal amplification. J Clin Microbiol 2006; 44: 3268-3273.
  • Nagai T, Okafuji T, Miyazaki C, Ito Y, Kamada M, Kumagai T, Yuri K, Sakiyama H, Miyata A, Ihara T, Ochiai H, Shimomura K, Suzuki E, Torigoe S, Igarashi M, Kase T, Okuno Y, Nakayama T. A comparative study of the incidence of aseptic meningitis in symptomatic natural mumps patients and monovalent mumps vaccine recipients in Japan. Vaccine 2007; 25: 2742-2747.
  • Naito Y, Higuchi M, Koinuma G, Aramaki M, Takahashi T, Kosaki K. Upper airway obstruction in neonates and infants with CHARGE syndrome, Am J Med Genet, 2007, 143:1815-1820.
  • Nakata Y, Shetzline S, Sakashita C, Kalota A, Rallapalli R, Rudnick SI, Zhang Y, Emerson SG and Gewirtz AM. c-Myb Contributes to G2/M Cell Cycle Transition in Human Hematopoietic Cells by Direct Regulation of Cyclin B1 Expression. Mol Cell Biol. 2007;27:2048-58.
  • Nakata Y, Kondoh K, Fukushima S, Hashiguchi A, Du W, Hayashi M, Fujimoto J, Hata J, Yamada Y. Mutated D4-guanine diphosphate-dissociation inhibitor (D4-GDI), is found in human leukemic cells, promotes leulemic cell invasion. Exp Hematol (in press).
  • Nakayama T, Onoda K. Vaccine adverse events reported in post-marketing study of the Kitasato Institute from 1994 to 2004. Vaccine 2007; 25: 570-576.
  • Narumi S, Amano N, Hachiya R, Ishii T, Hasegawa T. A novel mutation of androgen receptor gene in complete androgen insensitivity. Clin Pediatr Endocrinol 2007;16:59-61.
  • Narumi S, Shiihara T, Numakura C, Seiwa C, Nozaki N, Yamagata T, Momoi M, Hori N, Nishimura G, Hasegawa T. Two Japanese patients of osteoporosis-pseudoglioma syndrome with novel mutations in LRP5. Am J Med Genet (in press).
  • Niu D, Huang J, Li H, Liu K, Wang S, Chen Y, Udaka T, Izumi K, Kosaki K. Paternal gonadal mosaicism of NIPBL mutation in a father of siblings with Cornelia de Lange syndrome. Prenat Diagn, 2006; 26:1054-1057.
  • Obata S, Zwolska Z, Toyota E, Kudo K, Nakamura A, Kuratsuji T et al. Association of rpoB mutations with rifampicin resistance in Mycobacterium avium. Int J Antimicrob Agents 2006; 27: 32-39.
  • Ogata T, Tanaka T, Kagami M. Target height and target range for the Japanese children: revisited. Clin Pediatr Endocrinol (in press).
  • Okafuji T, Okafuji T, Fujino M, Nakayama T. Current status of measles in Japan: molecular and serological studies. J Infect Chemother 2006; 12: 343-348.
  • Omori S, Kitagawa H, Koike J, Fujita H, Hida M, Pringle KC, Awazu M. Activated ERK correlates with cyst formation and TGF-s expression in obstructive uropathy in fetal lambs. Kidney Int (in press).
  • Poduri A, Golja A, Takeoka M, Bourgeois BF, Connolly L, Riviello JJ Jr.. Focal cortical malformations can show asymmetrically higher uptake on interictal fluorine-18 fluorodeoxyglucose positron emission tomography (PET). J Child Neurol. 2007;22:232-7.
  • Samejima H, Torii C, Kosaki R, Kurosawa K, Yoshihashi H, Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi T, Kosaki K. Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography. Genet Test (in press).
  • SasakiG, IshiiT, Amano N, Hachiya R, Narumi S, Hasegawa T. Growth failure in an infant with congenital nephrogenic diabetes insipidus during sodium restriction. Clin Pediatr Endocrinol (in press).
  • Sato N, Kamachi Y, Kondoh H, Shima Y, Morohashi K, Horikawa R, Ogata T. Hypogonadotropic hypogonadism in an adult female with heterozygous hypomorphic mutation of SOX2. Eur J Endocrinol 2006;156:167-171.
  • Schunemann HJ, Hill SR, Kakad M, Bellamy R, Uyeki TM, Hayden FG, Yazdanpanah, Y. Beigel, J. Chotpitayasunondh, T. Del Mar, C. Farrar, J. Tran, T. H. Ozbay, B. Sugaya, N. Fukuda, K. Shindo, N. Stockman, L. Vist, G. E. Croisier, A. Nagjdaliyev, A. Roth, C. Thomson, G. Zucker, H. Oxman, A. D. WHO Rapid Advice Guidelines for pharmacological management of sporadic human infection with avian influenza A (H5N1) virus. Lancet Infect Dis. 2007;7:21-31.
  • Schunemann HJ, Hill SR, Kakad M, Vist GE, Bellamy R, Stockman L, Wisloff, T. F. Del Mar, C. Hayden, F. Uyeki, T. M. Farrar, J. Yazdanpanah, Y. Zucker, H. Beigel, J. Chotpitayasunondh, T. Hien, T. T. Ozbay, B. Sugaya, N. Oxman, A. D l. Transparent development of the WHO rapid advice guidelines. PLoS Med. 2007;4:e119.
  • Seishima M, Mizutani Y, Shibuya Y, Arakawa C, Yoshida R, Ogata T. Malignant melanoma in a female with LEOPARD syndrome: identification of a germline PTPN11 mutation of and a somatic BRAF mutation. Bri J Dermatol (in press).
  • Sekiguchi J, Asagi T, Miyoshi-Akiyama T, Kasai A, Mizuguchi Y, Kuratsuji T et al. Outbreaks of multidrug-resistant pseudomonas aeruginosa in community hospitals in Japan. J Clin Microbiol 2007; 45: 979-989.
  • Sekiguchi J, Miyoshi-Akiyama T, Augstynowicz-Kopek E, Zwolska Z, Kuratsuji T et al. Detection of multidrug resistance in Mycobacterium tuberculosis. J Clin Microbiol 2007; 45: 179-192.
  • Sekiguchi J, Fujino T, Araake M, Toyota E, Kudo K, Kuratsuji T et al. Emergence of rifampicin resistance in methicillin-resistant Staphylococcus aureus in tuberculosis wards. J Infect Chemother 2006; 12: 47-50.
  • Shiga M, Saito M, Hattori M, Torii C, Kosaki K, Kiyono T, Suda N. Characteristic phenotype of immortalized periodontal cells isolated from a Marfan syndrome type I patient. Cell Tissue Res (in press).
  • Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama, K. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2: Possible involvement of non-genetic or epigenetic regulation. Orthod Craniofac Res (in press).
  • Sugawara W, Haruta M, Sasaki F, Watanabe N, Tsunematsu Y, Kikuta A, Kaneko Y. Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma. Pediatr Blood Cancer. 2007;49:240-9.
  • Sugaya N, Mitamura K, Yamazaki M, Tamura D, Ichikawa M, Kimura K, Kawakami, C. Kiso, M. Ito, M. Hatakeyama, S. Kawaoka, Y. Lower clinical effectiveness of oseltamivir against influenza B contrasted with influenza A infection in children. Clin Infect Dis. 2007;44:197-202.
  • Suzuki K, Haraguchi R, Ogata T, Barbieri O, Alegria O, Vieux-Rochas M, Nakagata N, Ito M, Mills A, Kurita T, Levi G, Yamada G. Abnormal urethra formation as a model for hypospadias of the split-hand-foot malformation (SHFM). Eur J Hum Genet (in press).
  • Tanaka Y, Hanada K, Hanabusa H, Kurbanov F, Gojobori T, Mizokami M. Increasing genetic diversity of hepatitis C virus in haemophiliacs with human immunodeficiency virus coinfection. J Gen Virol. 2007;88:2513-9.
  • Torii C, Izumi K, Nakajima H, Takahashi T, Kosaki K. EFNB1 mutation at the ephrin ligand - ephrin receptor dimerization interface in a patient with craniofrontonasal syndrome, Congenit Anomal, 2007; 47:49-52.
  • Udaka T, Issei I, Aizu Y, Torii C, Izumi K, Kosaki R, Takahashi T, Hayashi S, Inazawa J, Kosaki K. Multiplex PCR/liquid Chromatography Assay for Screening of Subtelomeric Rearrangements. Genet Test (in press).
  • Udaka T, Kurosawa K, Izumi K, Yoshida S, Tsukahara M, Okamoto N, Torii C, Kosaki R, Masuno M, Hosokai N, Takahashi T, Kosaki K. Screening for partial deletions of CREBBP locus in Rubinstein-Taybi Syndrome patients using multiplex PCR / Liquid chromatography, Genet Test, 2006; 10:265-71.
  • Udaka T, Okamoto N, Aramaki M, Torii C, Kosaki R, Hosokai N, Hayakawa T, Takahata N, Takahashi T, Kosaki K. An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome. Am J Med Genet, 2007; 143:721-726.
  • Yamazawa K, Kodo K, Maeda J, Omori S, Hida M, Mori T, Awazu M. Hyponatremia, hypophosphatemia, and hypouricemia in a girl with macrophage activation syndrome. Pediatrics 2006;118:2557-2560.
  • Yamamoto K, Yoshida R, Ogata T. KRAS analysis in 34 PTPN11 mutation negative Noonan syndrome patients. Clin Pediatr Endocrinol (in press).
  • Yamazawa K, Kagami M, Ogawa M, Horikawa R, Ogata T. Placental hypoplasia in maternal uniparental disomy for chromosome. Am J Med Genet A (in press).
  • Yamazawa K, Wada Y, Sasagawa I, Aoki K, Ueoka K, Ogata T. Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism. Homr Res (in press).
  • Yoshida R, Ogata T, Masawa N, Nagai T. Hepatoblastoma in a patient with PTPN11 mutation positive Noonan syndrome. Pediatr Blood Cancer (in press).
  • Yoshida N, Fujino M, Ota Y, Notomi T, Nakayama T. Simple differentiation method of mumps Hoshino vaccine strain from wild strains by reverse transcription loop-mediated isothermal amplification (RT-LAMP). Vaccine 2007; 25: 1281-1286.
  • Yoshii A, Constantine-Paton M. BDNF induces transport of PSD-95 to dendrites through PI3K-AKT signaling after NMDA receptor activation. Nat Neurosci. 2007;10:702-11.
  • Watanabe M, Yoshida R, Ueoka K, Aoki K, Sasagawa I, Hasegawa T, Sueoka K, Kamitsuji S, Kamatani N, Yoshimura Y, Ogata T. Haplotype analysis of the estrogen receptor ? gene in male genital and reproductive abnormalities: implications for the susceptibility to estrogenic environmental endocrine disruptors. Hum Reprod 2007;22:1279-1284.
  • Whitsett JA, Matsuzaki Y. Transcriptional regulation of perinatal lung maturation. Pediatr Clin North Am. 2006 53:873-87, viii. Review.