研究業績

Publications 2002

  • Abe M, Tamamura Y, Yamagishi H, Maeda T, Kato J, Tabata MJ, Srivastava D, Wakisaka S, Kurisu K :Tooth-type specific expression of dHAND/Hand2 possible involvement in murine lower incisor morphogenesis Cell Tissue Res 310201-212,2002
  • Abe Y, Takamura M, Sawada M, Hisano M, Tsuji Y, Saikawa N, Okuyama T, Odajima Y, Fujita K, Chikaoka H, Iikura Y :Case of insertion, inversion and deletion of chromosome 6. Pediatr Int 44:530-533,2002
  • Anzo M, Takahashi T, Sato S, Matsuo N :The cross-sectional head circumference growth curves for Japanese from birth to 18 years of age the 1990 and 1992-1994 national survey data. Ann Hum Biol 29:373-88,2002
  • Awazu M, Fujita H, Omori S, Hida M :The herbal medicine Sairei-to inhibits proliferation of rat mesangial cells. Nephron 92:652-659,2002
  • Awazu M, Omori S, Hida M :MAP kinase in renal development. Nephrol Dial Transplant 17(Suppl9):5-7,2002
  • Cai L, Hayes NL, Takahashi T, Caviness VS Jr, Nowakowski RS :Size distribution of retrovirally marked lineages matches prediction from population measurements of cell cycle behavior J Neurosci Res 69731-44,2002
  • Fujino M, Li XK, Guo L, Kitazawa Y, Funeshima N, Fukuda S, Kimura H, Miyashita T, Okuyama T, Amano T, Suzuki S :T-cell apoptosis triggered by FTY720 via mitochondrial pathway. Transplant Proc 33:3084-3085,2002
  • Fujita H, Kosaki R, Yoshihashi H, Ogata T, Tomita M, Hasegawa T, Takahashi T, Matsuo N, Kosaki K. :Characterization of the aryl hydcrocarbon receptor repressor gene and association of its Pro185Ala olymorphism with micropenies. Teratology 65:10-18,2002
  • Fukuzawa R, Sato S, Sullivan MJ, Nishimura G, Hasegawa T, Matsuo N :Autopsy case of microcephalic osteodysplastic primordial dwarfism type II. Am J Med Genet 113:93-96,2002
  • Goto T, Takahashi T, Miyama S, Nowakowski RS, Bhide PG, Caviness VS Jr. :Developmental regulation of the effects of fibroblast growth factor-2 and 1-octanol on neuronogenesis: implications for a hypothesis relating to mitogen-antimitogen opposition. J Neurosci Res 69:714-722,2002-9
  • Gottlieb PD, Pierce SA, Sims RJ, Yamagishi H, Weihe EK, Harriss JV, Maika SD , Kuziel WA , King HL, Olson EN, Nakagawa O, Srivastava D :Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis Nat Genet 3125-32,2002
  • Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, IdaT, Yoshiura K-I, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N :Duplication of 8p23.2: a benign cytogenetic variant ? Am J Med Genet 111:285-288,2002
  • Hattori S, Yoshioka K, Honda M, Ito H :on behalf of the Japanese Society for Pediatric Nephrology: The 1998 report of the Japanese National Registry date on pediatric end-stage renal disease patients. Pediatr Nephrol 17:456-461,2002
  • Herbert MR, Harris GJ, Adrien KT, Ziegler DA, Makris N, Kennedy DN, Lange NT, Chabris CF, Bakardjiev A, Hodgson J, Takeoka M, Tager Flusberg H, Caviness VS Jr :Abnormal asymmetry in language association cortex in autism. Ann Neurol 52:588-596,2002
  • Hida M, Omori S, Awazu M :ERK and p38 MAP kinase are required for rat renal development Kidney Int 611:252-1262,2002
  • Hida M, Omori S, Awazu M :Extracellular signal regulated kinase and p38 mitogen activated protein kinase are required for rat renal development. Kidney Int 61:1252-1262,2002
  • Higuchi A, Kawamura T, Nakai H, Hasegawa Y :Infrequent voiding in nephrogenic diabetes insipidus as a cause of renal failure. Pediatr Int 44:540-542,2002
  • Honda M :Nephrotic syndrome and mizoribine in children. Pediatr Int 44:210-216,2002
  • Hoshii S, Honda M :High incidence of encapsulating peritoneal sclerosis in pediatric patients on peritoneal dialysis longer than 10 years. Perit Dial Int 22:730-731,2002-11-12
  • Ikeda M, Yata N, Kamei K, Mori K, Ishikura K, Hataya H, Honda M, Asanuma H, Shishido S, Nakai H :Posterior leukoencephalopathy syndrome in pediatric patients with kidney disease. Pediatr Nephrol 17:71,2002-1
  • Iitaka K, Moriya S, Nakamura S, Tomonaga K, Sakai T :Long-term follow-up of type III membranoproliferative glomerulonephritis in children. Pediatr Nephrol 17:373-378,2002
  • Ikeda K, Hokuto I, Tokieda K, Nishimura O, Ishimoto H, Morikawa Y :A congenital anterior diaphragmatic hernia with massive pericardialeffusion requiring neither emergency pericardiocentesis nor operation.A case report and review of the literature. J Perinat Med 30:336-340,2002
  • Inokuchi M, Hasegawa T, Hori N, Choe M-s, Tokita N, Watanabe H, Matsuo N :Lack of correlation between the endocrinological abnormalities and obesity index in anorexia nervosa in childhood and adolescence Clin Pediatr Endocrinol 11(Suppl17)73-75,2002
  • Ishii T, Hasegawa T, Pai C-I, Yvgi-Ohana N, Timberg R, Zhao L, Majdic G, Chung B-c, Orly JC, Parker KL :The roles of circulating high density lipoproteins and trophic hormones in the phenotype of knockout mice lacking the steroidogenic acute regulatory protein Mol Endocrinol 162297-2309,2002
  • Ito H, Tae T, Honda M, Igarashi T, Joh K, Hashizume T, Yamaoka K :Preventive effect of TAK-751S on complications of hemorrhagic colitis (Results of clinical study of TAK-751S) JP J Antibiotics 55203-227,2002
  • Ito K, Matsuyama T :The single-plasma -sample method for determining the glomerular filtration rate with Tc-99m-DTPA in childhood and adolescenceIs it age-related? Ann Nucl Med 16541-548,2002
  • Itoh K, Sasagawa I, Suzuki Y, Ashida J, Nakada T, Ogata T :Mutation screening of 5a-reductase type 2 gene in Japanese men with idiopathic azoospermia. Fertil Steril 77:1079-1080,2002
  • Kamimaki I, Shishido S, Ikeda M, Honda M :Histopathological findings of 10-year protocol biopsy in pediatric kidney transplant recipients. Transplant Proc 34:3130-3131,2002-12
  • Kitamura K, Yanazawa M, Sugiyama N, Miura H, Iizuka-Kogo A, Kusaka M, Omichi K, Suzuki R, Kato-Fukui Y, Kamiirisa K, Matsuo M, Kamijo S, Kasahara M, Yoshioka H, Ogata T, Fukuda T, Kondo I, Kato M, Dobyns WB, Yokoyama M, Morohashi K :Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans Nat Genet 32359-369,2002
  • Kosaki K, Suzuki T, Muroya K, Hasegawa T, Sato S, Matsuo N, Kosaki R, Nagai T, Hasegawa Y, Ogata T :PTPN11 (Protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome. J Clin Endocrinol Metab 87:3529-3533,2002-8
  • Kondoh K, Nakata Y, Hosoda F, Gamou T, Kurosawa Y, Kinoshita A, Ohki M, Tomita Y, Mori T :A pediatric case of secondary leukemia associated with t(16;21)(q24;q22) exhibiting the chimeric AML1-MTG16 gene. Leukemia Lymphoma 43:415-420,2002
  • Kosaki K, Kosaki R, Suzuki T, Yoshihashi H, Takahashi T, Sasaki K, Tomita M, McGinnis W, Matsuo N :Complete mutation analysis panel of > the 39 human HOX genes. Teratology 65:50-62,2002
  • Kosaki K, Ogata T, Kosaki R, Sato S, Matsuo N :A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome Differential role of the polyalanine tract in the development of the ovary and the eyelid Ophthalmic Genet 2343-47,2002
  • Kosho T, Uemura T, Tanimura M, Ohashi H, Muroya K, Ogata :Refined mapping of the gene for otopalatodigital syndrome type I. J Med Genet 39:E7,2002
  • Kubota T, Wakui K, Nakamura T, Ohashi H, Watanabe Y, Yoshino M, Kida T, Okamoto N, Matsumura M, Muroya K, Ogata T, Goto Y, Fukushima Y :The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females Cytogenet Genome Res 99276-284,2002
  • Kurosawa K, Sasaki H, Sato Y, Yamanaka M, Shimizu M, Ito Y, Okuyama T, Matsuo M, Imaizumi K, Kuroki Y, Nishimura G :Paternal UPD14 is responsible for a distinctive malformation complex. Am J Med Genet 110:268-272,2002
  • Li XK, Kosuga M, Tokieda K, Kanaji A, Fukuhara Y, Hashimoto M, Okabe K, Yaginuma H, Yamada M, Suzuki S, Okuyama T :Prolongation of transgene expression by coexpression of cytokine response modifier a in rodent liver after adenoviral gene transfer Mol Ther 5262-268,2002
  • Matsuoka S, Kawamura K, Honda M, Awazu M :White coat phenomenon in normotensive and hypertensive children and Adolescents. Pediatr Nephrol 7:950-953,2002
  • Miura T, Kimura K, Nakayama T :Incidence of adverse reactions associated with gelatin in vaccination. Medical Postgraduate 40:367-370,2002
  • Miyamoto J, Hasegawa Y :Male pseudohermaphroditism due to disorder of androgen receptor function:X Nippon Rinsho 60 367-72,2002
  • Mori K, Ikeda K, Tanaka M :Different expression of surfactant protein B mature peptide and proprotein at 21 weeks' gestation in human fetal pulmonary epithelial cells Pediatrics international 44500-504,2002
  • Mori K, Kurihara N, Hayashida S, Tanaka M, Ikeda K :The intrauterine expression of surfactant protein D in the terminal airways of human fetuses compared with surfactant protein A Eur J Pediatr 161431-434,2002
  • Mori K, Kurihara N, Obi S, Hayashida S, Tokieda K, Ikeda K :Intratracheal instillation of perfluorocarbon rescued mice with primary pulmonary hypoplasia. Exp Lung Res 28:523-533,2002
  • Motoyama O, Shigetomi Y, Ohara A, Iitaka K :A boy with recurrent hemorrhagic cystitis during treatment with Chinese herbel medicine. Clin Exp Nephrol 6:121-124,2002
  • Muroya K, Nishimura G, Douya H, Hasegawa T, Ogata T :Diaphyseal medullary stenosis with malignant fibrous histiocytoma Further evidence for loss of heterozygosity involving 9p21-22 in tumor tissue Genes Chromosomes Cancer 33326-328,2002
  • Muroya K, Yamamoto K, Fukushima Y, Ogata T :Ring chromosome 21 in a boy and a derivative chromosome 21 in the mother: Implication for ring chromosome formation. Am J Med Genet 110:332-337,2002-7
  • Norden AG, Lapsley M, Igarashi T, Kelleher CL, Lee PJ, Matsuyama T, Scheinman SJ, Shiraga H, Sundin DP, Thakker RV, Unwin RJ, Verroust P, Moestrup SK :Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome. J Am Soc Nephrol 13:125-133,2002-12
  • Norden A, Lapsley M, Igarashi T, Kelleher C, Lee P, Matsuyama T, Scheinman S, Shiraga H, Sundin D, Thakker R, Unwin R, Verroust P, Moestrup S :Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome J Am Soc Nephrol 13:125-133,2002
  • Norden AG, Lapsley M, Igarashi T, Kelleher CL, Lee PJ, Matsuyama T, Scheinman SJ, Shiraga H, Sundin DP, Thakker RV, Unwin RJ, Verroust P :Moestrup SK Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome J Am Soc Nephrol 13125-133,2002
  • Nowakowski RS, Caviness VS Jr, Takahashi T, Hayes NL :Population dynamics during cell proliferation and neuronogenesis in the developing murine neocortex. Results Probl Cell Differ 39:1-25,2002
  • Ogata T :SHOX haploinsufficiency: lessons from clinical studies. Current Opinion in Endocrinology and Diabetes 9:13-20,2002
  • Ogata T :SHOX haploinsufficiency and its modifying factors. J Pediatr Endocrinol Metab 15:1289-1294,2002
  • Ogata T, Muroya K, Sasaki G, Nishimura G, Kitoh H, Hattori T :SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features. J Clin Endocrinol Metab 87:1390-1394,2002-3
  • Ogata T, Inokuchi M, Ogawa M :Growth pattern and body proportion in a female with short stature homeobox-containing gene overdosage and gonadal estrogen deficiency Eur J Endocrinol 147249-254,2002
  • Omori S, Fukuzawa R, Hida M, Awazu M :Expression of mitogen−activatedprotein kinases in human renal dysplasia. Kidney Int 61:899-906,2002
  • Rappold GA , Fukami M, Niesler B, Schiller S, Zumkeller W, Bettendorf M, Heinrich U, Vlachopapadoupoulou E, Reinehr T, Onigata K, Ogata T :eletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature. D J Clin Endocrinol Metab 87:1402-1406,2002
  • Sano Y, Yamada J, Ishino Y, Adachi W, Kawasaki S, Suzuki T, Kinoshita S, Okuyama T, Azuma N :Non-cleavable mutant Fas ligand transfection of donor cornea abrogates ocular immune privilege. Exp Eye Res 75:475-483,2002
  • SATO Y, TOYONAGA Y, SUNAKAWA K et al :Spread of Penicillin-resistant Streptococcus pneumoniae (PRSP) and Beta-lactamase-negative Ampicillin-resistant Haemophilus influenzae (BLNAR) in Pediatrics.  ICAAC 42:27-30,2002-9
  • Sonoda S, Kitahara M, Nakayama T :Detection of measles virus genome in bone-marrow aspirates from adults. J Gen Virol 83(Pt 10):2485-2488,2002-10
  • Sasagawa I, Suzuki Y, Muroya K, Ogata T :Androgen receptor gene and male genital anomaly. Arch Androl 48:461-466,2002-11
  • Sugita K, Kato Y, Sugita K, Kato M, Tanaka Y :Magnetoencephalographic analysis in a case of early-onset benign childhood occipital seizures. J Child Neurol 17:851-852,2002-11
  • Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N :Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome. Am J Med Genet 110:365-369,2002
  • Sekino T, Kiyokawa N, Taguchi T, Ohmi K, Nakajima H, Suzuki T, Furukawa S, Nakao H, Takeda T, Fujimoto J :Inhibition of Shiga toxin cytotoxicity in human renal cortical epithelial cells by nitrobenzylthioinosine J Infec Dis 185:785-796,2002
  • Shimada H, Ichikawa H, Ohki M :Potential involvement of the AML1-MTG8 fusion protein in the granulocytic maturation characteristic of the t(8;21) acute myelogenous leukemia revealed by microarray analysis Leukemia 16874-875,2002
  • Shin CH, Liu ZP, Passier R, Zhang CL, Wang DZ, Harris TM, Yamagishi H, Richardson JA, Childs G, Olson EN :Modulation of cardiac growth and development by HOP, an unusual homeodomain protein. Cell 110:725-735,2002
  • Shinjoh M, Yoshikawa T, Li Y, Shiraishi K, Ueki H, Nerome K :Prophylaxis and treatment of influenza encephalitis in an experimental mouse model. J Med Virol 67:406-417,2002
  • Sugaya N, Yoshikawa T, Miura M, Ishizuka T, Kawakami C, Asano Y :Influenza encephalopathy associated with infection with human herpesvirus 6 and/or human herpesvirus 7. Clin Infect Dis 34:461-466,2002
  • Suzuki Y, Sasagawa I, Itoh K, Ashida J, Ogata T :5α-reductase type 2 genes in Japanese males do not appear to be associated with cryptorchidism. Fertil Steril 78:330-334,2002
  • Suzuki Y, Sasagawa I, Itoh K, Ashida J, Muroya K, Ogata T :Estrogen receptor alpha gene polymorphism is associated with idiopathic azoospermia. Fertil Steril 78:1341-1343,2002-12
  • Takahashi T, Caviness VS Jr, Bhide PG :Analysis of cell generation in the telencephalic neuroepithelium. Methods Mol Biol 198:101-113,2002
  • Takahashi T, Watanabe H, Matsuo N :Psychosomatic disorders in children:an emerging challenge to health care in Japan . Methods Mol Biol 44:153-156,2002
  • Takeoka M, Riviello JJ, Pfeifer H, Thiele EA :Concomitant treatment with topiramate and the ketogenic diet in pediatric epilepsy. Epilepsia 43:1072-1075,2002
  • Takeoka M, Takahashi T :Infectious and inflammatory disorders of the circulatory system and stroke in childhood. Curr Opin Neurol 15:159-164,2002
  • Takeoka M, Soman TB, Yoshii A, Caviness VS Jr, Gonzalez RG, Grant PE, Krishnamoorthy KS :Diffusion-weighted images in neonatal cerebral hypoxic-ischemic injury. Pediatr Neurol 26:274-281,2002-4
  • Tamai S, Tojo M, Kamimaki T, Sato Y, Nishimura G :Intrafamilial phenotypic variations in cranioectodermal dysplasia: propositus with typical manifestations and her brother with perinatal death. Am J Med Genet 107:78-80,2002
  • Tanaka Y, Hataya H, Araki Y, Ikeda M, Matsuyama T, Honda M :Hyperlipidemia in children on peritonial dialysis : Effect of energy intake on serum triglyceride. Peritoneal Dialysis International 22:426-428,2002
  • Tokumura M, Yoshiba S, Kojima Y, NanriS :Impaired cardiorespiratory response to brief sudden strenuous exercise in the postoperative tetralogy of Fallot patients: a ten-second pedaling test Pediatr Cardiol 23:496-501,2002
  • Yamagishi H :The 22q11.2 deletion syndrome. Keio J Med 51:77-88,2002
  • Yamagishi H, Maeda Jun, Higuchi M, Katada Y, Yamagishi C, Matsuo N, Kojima Y :Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q112 deletion Clin Genet 62214-219,2002