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2009 2008  2007  2006  2005  2004  2003  2002  2001  2000


2011

  1. Inoue H, Kangawa N, Kinouchi A, Sakamoto Y, Kimura C, Horikawa R, Shigematsu Y, Itakura M, Ogata T, Fujieda K; Japan Growth Genome Consortium: Identification and functional analysis of novel human growth hormone-releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature. Clin Endocrinol (Oxf). 2011;74:223-233.

  2. Inoue H, Kangawa N, Kinouchi A, Sakamoto Y, Kimura C, Horikawa R, Shigematsu Y, Itakura M, Ogata T, Fujieda K; Japan Growth Genome Consortium: Identification and functional analysis of novel human growth hormone secretagogue receptor (GHSR) gene mutations in Japanese subjects with short stature. J Clin Endocrinol Metab. 2011;96:E373-378.

  3. Inoue H, Sakamoto Y, Kangawa N, Kimura C, Ogata T, Fujieda K, Qian ZR, Sano T, Itakura M: Analysis of expression and structure of the rat GH-secretagogue/ghrelin receptor (Ghsr) gene: Roles of epigenetic modifications in transcriptional regulation. Mol Cell Endocrinol. 2011;345:1-15

  4. Inoue H, Mukai T, Sakamoto Y, Kimura C, Kangawa N, Itakura M, Ogata T, Ito Y, Fujieda K: Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT-1 gene in Japanese identical twins with mild combined pituitary hormone deficiency. Clin Endocrinol (Oxf), 2011.

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2010

  1. Nishimoto K, Kochi Y, Ikari K, Yamamoto K, Suzuki A, Shimane K, Nakamura Y, Yano K, Iikuni N, Tsukahara S, Kamatani N, Okamoto H, Kaneko H, Kawaguchi Y, Hara M, Toyama Y, Horiuchi T, Tao K, Yasumoto K, Hamada D, Yasui N, Inoue H, Itakura M, Yamanaka H, Momohara S: Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese. Ann Rheum Dis. 2010;69:368-373.

  2. Bolduc V, Marlow G, Boycott KM, Saleki K, Inoue H, Kroon J, Itakura M, Robitaille Y, Parent L, Baas F, Mizuta K, Kamata N, Richard I, Linssen WH, Mahjneh I, de Visser M, Bashir R, Brais B: Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies. Am J Hum Genet. 2010;86:213-221. 

  3. Muroya K, Mochizuki T, Fukami M, Iso M, Fujita K, Itakura M, Ogata T: Diabetes Mellitus in a Japanese Girl with HDR Syndrome and GATA3 Mutation. Endocr J.  2010;57:171-174.

  4. Numata S, Nakataki M, Iga JI, Tanahashi T, Nakadoi Y, Ohi K, Hashimoto R, Takeda M, Itakura M, Ueno SI, Ohmori T: Association Study Between the Pericentrin (PCNT) Gene and Schizophrenia. Neuromolecular Med.2010;12:243-247.

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2009

  1. Iwata T, Kuwajima M, Sukeno A, Ishimaru N, Hayashi Y, Wabitsch M, Mizusawa N, Itakura M, Yoshimoto K: YKL-40 secreted from adipose tissue inhibits degradation of type I collagen. Biochem Biophys Res Commun. 2009;388:511-516.

  2. Numata S, Iga JI, Nakataki M, Tayoshi S, Taniguchi K, Sumitani S, Tomotake M, Tanahashi T, Itakura M, Kamegaya Y, Tatsumi M, Sano A, Asada T, Kunugi H, Ueno SI, Ohmori T: Gene expression and association analyses of the phosphodiesterase 4B (PDE4B) gene in major depressive disorder in the Japanese population. Am J Med Genet B Neuropsychiatr Genet. 2009;150B:527-534.

  3. Qian ZR, Asa SL, Siomi H, Siomi MC, Yoshimoto K, Yamada S, Wang EL, Rahman MM, Inoue H, Itakura M, Kudo E, Sano T: Overexpression of HMGA2 relates to reduction of the let-7 and its relationship to clinicopathological features in pituitary adenomas. Mod Pathol. 2009;22:431-441.

  4. Otsuka S, Sakamoto Y, Siomi H, Itakura M, Yamamoto K, Matumoto H, Sasaki T, Kato N, Nanba E.:Fragile X carrier screening and FMR1 allele distribution in the Japanese population. Brain Dev. 2009 

  5. nese population.  Brain Dev. 2009  ( in press )

  6. Nishimoto K, Kochi Y, Ikari K, Yamamoto K, Suzuki A, Shimane K, Nakamura Y, Yano K, Iikuni N, Tsukahara S, Kamatani N, Okamoto H, Kaneko H, Kawaguchi Y, Hara M, Toyama Y, Horiuchi T, Tao K, Yasumoto K, Hamada D, Yasui N, Inoue H, Itakura M, Yamanaka H, Momohara S: Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese.   Ann Rheum Dis. 2009 (in press)

  7. Nakataki M, Numata S, Iga J, Tayoshi S, Tayoshi-Shibuya S, Song H, Tanahashi T, Itakura M, Ueno S, Ohmori T: No association between Rho-associated coiled-coil forming protein serine/threonine kinase1 gene and schizophrenia in the Japanese population.  Psychiatr Genet. 2009;19(3):162.

  8. Numata S, Ueno SI, Iga JI, Song H, Nakataki M, Tayoshi S, Sumitani S, Tomotake M, Itakura M, Sano A, Ohmori T: Positive association of the PDE4B (phosphodiesterase 4B) gene with schizophrenia in the Japanese population.  J Psychiatr Res.  2009;43:7-12.  

  9. Numata S, Iga J, Nakataki M, Tayoshi S, Tanahashi T, Itakura M, Ueno S, Ohmori T: Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population. J Psychiatry Neurosci. 2009;34:195-198.

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2008

  1. Yasuda K, Miyake K, Horikawa Y, Hara K, Osawa H, Furuta H, Hirota Y, Mori H, Jonsson A, Sato Y, Yamagata K, Hinokio Y, Wang HY, Tanahashi T, Nakamura N, Oka Y, Iwasaki N, Iwamoto Y, Yamada Y, Seino Y, Maegawa H, Kashiwagi A, Takeda J, Maeda E, Shin HD, Cho YM, Park KS, Lee HK, Ng MC, Ma RC, So WY, Chan JC, Lyssenko V, Tuomi T, Nilsson P, Groop L, Kamatani N, Sekine A, Nakamura Y, Yamamoto K, Yoshida T, Tokunaga K, Itakura M, Makino H, Nanjo K, Kadowaki T, Kasuga M: Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Nat Genet. 2008;40:1092-1097 

  2. Kondoh K, Nakata Y, Yamaoka T, Itakura M, Hayashi M, Yamada K, Hata JI, Yamada T: Altered cellular immunity in transgenic mice with T cell-specific expression of human D4-guanine diphosphate-dissociation inhibitor (D4-GDI). Int Immunol. 2008;20:1299-1311

  3. Miyawaki K, Inoue H, Keshavarz P, Mizuta K, Sato A, Sakamoto Y, Moritani M, Kunika K, Tanahashi T, Itakura M: Transgenic expression of a mutated cyclin-dependent kinase 4 (CDK4/R24C) in pancreatic beta-cells prevents progression of diabetes in db/db mice. Diabetes Res Clin Pract. 2008;82:33-41

  4. Kobayashi S, Ikari K, Kaneko H, Kochi Y, Yamamoto K, Shimane K, Nakamura Y, Toyama Y, Mochizuki T, Tsukahara S, Kawaguchi Y, Terai C, Hara M, Tomatsu T, Yamanaka H, Horiuchi T, Tao K, Yasutomo K, Hamada D, Yasui N, Inoue H, Itakura M, Okamoto H, Kamatani N, Momohara S: Association of STAT4 with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Japanese population. Arthritis Rheum. 2008;58:1940-1946.

  5. Yamaguchi Y, Moritani M, Tanahashi T, Osabe D, Nomura K, Fujita Y, Keshavarz P, Kunika K, Nakamura N, Yoshikawa T, Ichiishi E, Shiota H, Yasui N, Inoue H, Itakura M: Lack of association of genetic variation in chromosome region 15q14-22.1 with type 2 diabetes in a Japanese population. BMC Med Genet. 2008;9:22

  6. Tanahashi T, Shinohara K, Keshavarz P, Yamaguchi Y, Miyawaki K, Kunika K, Moritani M, Nakamura N, Yoshikawa T, Shiota H, Inoue H, Itakura M: The association of genetic variants in Krüppel-like factor 11 and Type 2 diabetes in the Japanese population. Diabet Med. 2008;25:19-26.

  7. Numata S, Ueno SI, Iga JI, Nakataki M, Tanahashi T, Itakura M, Sano A, Ohi K, Hashimoto R, Takeda M, Ohmori T: No association between the NDE1 gene and schizophrenia in the Japanese population.  Schizophr Res. 2008;99:367-369.

  8. Suzuki T, Moritani M, Yoshino M, Kagami M, Iwasaki S, Nishimura K, Akamatsu M, Kobori M, Matsushime H, Kotoh M, Furuichi K, Itakura M: Diabetic modifier QTLs in F(2) intercrosses carrying homozygous transgene of TGF-beta.  Mamm Genome. 2008;19:15-25.

  9. Takata Y, Inoue H, Sato A, Tsugawa K, Miyatake K, Hamada D, Shinomiya F, Nakano S, Yasui N, Tanahashi T, Itakura M: Replication of reported genetic associations of PADI4, FCRL3, SLC22A4 and RUNX1 genes with rheumatoid arthritis: results of an independent Japanese population and evidence from meta-analysis of East Asian studies.  J Hum Genet. 2008;53:163-173.

  10. Keshavarz P, Inoue H, Nakamura N, Yoshikawa T, Tanahashi T, Itakura M: Single nucleotide polymorphisms in genes encoding LKB1 (STK11), TORC2 (CRTC2) and AMPK alpha2-subunit (PRKAA2) and risk of type 2 diabetes. Mol Genet Metab  2008;9:200-209.

  11. Numata S, Ueno SI, Iga JI, Yamauchi K, Hongwei S, Hashimoto R, Takeda M, Kunugi H, Itakura M, Ohmori T: TGFBR2 gene expression and genetic association with schizophrenia.  J Psychiatr Res 2008;42:425-432.

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2007

  1. Yamasaki S, Kurita N, Hata J, Moritani M, Itakura M, Shimada M: The effect of transgenic expression of TGF-beta1 on transplanted islet graft survival. Hepatogastroenterology 2007;54:1617-1621.

  2. Song H, Ueno SI, Numata S, Iga JI, Shibuya-Tayoshi S, Nakataki M, Tayoshi S, Yamauchi K, Sumitani S, Tomotake T, Tada T, Tanahashi T, Itakura M, Ohmori T: Association between PNPO and schizophrenia in the Japanese population.  Schizophr Res 2007;97:264-270.

  3. Sakamoto Y, Inoue H, Keshavarz P, Miyawaki K, Yamaguchi Y, Moritani M, Kunika K, Nakamura N, Yoshikawa T, Yasui N, Shiota H, Tanahashi T, Itakura M: SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population. J Hum Genet 2007;52:781-793.

  4. Ochi M, Osawa H, Hirota Y, Hara K, Tabara Y, Tokuyama Y, Shimizu I, Kanatsuka A, Fujii Y, Ohashi J, Miki T, Nakamura N, Kadowaki T, Itakura M, Kasuga M, Makino H: The frequency of the G/G genotype of resistin single nucleotide polymorphism at -420 appears to be increased in younger onset type 2 diabetes. Diabetes 2007;56:2834-2838.

  5. Miyatake K, Inoue H, Hashimoto K, Takaku H, Takata Y, Nakano S, Yasui N, Itakura M: PKC412 (CGP41251) modulates the proliferation and lipopolysaccharide-induced inflammatory responses of RAW 264.7 macrophages.  Biochem Biophys Res Commun 2007;360:115-121.

  6. Osabe D, Tanahashi T, Nomura K, Shinohara S, Nakamura N, Yoshikawa T, Shiota H, Keshavarz P, Yamaguchi Y, Kunika K, Moritani M, Inoue H, Itakura M: Evaluation of sample size effect on the identification of haplotype blocks. BMC Bioinformatics 2007;14;8:200.

  7. Inouchi A, Shinohara S, Inoue H, Kita K, Itakura M: Identification of specific sequence motifs in the upstream region of 242 human miRNA genes. Comput Biol Chem 2007;31:207-214.

  8. Mizuta K, Tsutsumi S, Inoue H, Sakamoto Y, Miyatake K, Miyawaki K, Noji S, Kamata N, Itakura M: Molecular characterization of GDD1/TMEM16E, the gene product responsible for autosomal dominant gnathodiaphyseal dysplasia. Biochem Biophys Res Commun 2007;357:126-132.

  9. Moritani M, Nomura K, Tanahashi T, Osabe D, Fujita Y, Shinohara S, Yamaguchi Y, Keshavarz P, Kudo E, Nakamura N, Yoshikawa T, Ichiishi E, Takata Y, Yasui N, Shiota H, Kunika K, Inoue H, Itakura M: Genetic association of single nucleotide polymorphisms in endonuclease G-like 1 gene with type 2 diabetes in a Japanese population. Diabetologia 2007;50:1218-1227.

  10. Iwata T, Mizusawa N, Taketani Y, Itakura M, Yoshimoto K: Parafibromin tumor suppressor enhances cell growth in the cells expressing SV40 large T antigen. Oncogene 2007;26:6176-6183.

  11. Hagiwara H, Sawakami-Kobayashi K, Yamamoto M, Iwasaki S, Sugiura M, Abe H, Kunihiro-Ohashi S, Takase K, Yamane N, Kato K, Son R, Nakamura M, Segawa O, Yoshida M, Yohda M, Tajima H, Kobori M, Takahama Y, Itakura M, Machida M: Development of an automated SNP analysis method using a paramagnetic beads handling robot. Biotechnol Bioeng 2007;98:420-428.

  12. Numata S, Ueno SI, Iga JI, Yamauchi K, Hongwei S, Hashimoto R, Takeda M, Kunugi H, Itakura M, Ohmori T: Gene expression in the peripheral leukocytes and association analysis of PDLIM5 gene in schizophrenia. Neurosci Lett 2007;415:28-33.

  13. Numata S, Ueno S, Iga J, Yamauchi K, Hongwei S, Kinouchi S, Shibuya-Tayoshi S, Tayoshi S, Aki H, Sumitani S, Itakura M, Ohmori T: Interaction between catechol-O-methyltransferase (COMT) Val108/158Met and brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in age at onset and clinical symptoms in schizophrenia. J Neural Transm 2007;114:255-259

  14. Takata Y, Hamada D, Miyatake K, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Osabe D, Moritani M, Kunika K, Kamatani N, Inoue H, Yasui N, Itakura M: Genetic association between the PRKCH gene encoding protein kinase Ceta isozyme and rheumatoid arthritis in the Japanese population. Arthritis Rheum 2007;56:30-42.

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2006

  1. Sakamoto Y, Inoue H, Kawakami S, Miyawaki K, Miyamoto T, Mizuta K, Itakura M: Expression and distribution of Gpr119 in the pancreatic islets of mice and rats: Predominant localization in pancreatic polypeptide-secreting PP-cells. Biochem Biophys Res Commun 2006;351:474-480.

  2. Kunika K, Tanahashi T, Kudo E, Mizusawa N, Ichiishi E, Nakamura N, Yoshikawa T, Yamaoka T, Yasumo H, Tsugawa K, Moritani M, Inoue H, Itakura M: Effect of +36T > C in intron 1 on the glutamine: fructose-6-phosphate amidotransferase 1 gene and its contribution to type 2 diabetes in different populations. J Hum Genet 2006;51:1100-1109.

  3. Takeshita S, Moritani M, Kunika K, Inoue H, Itakura M: Diabetic modifier QTLs identified in F(2) intercrosses between Akita and A/J mice. Mamm Genome 2006;17:927-940

  4. Tanahashi T, Osabe D, Nomura K, Shinohara S, Kato H, Ichiishi E, Nakamura N, Yoshikawa T, Takata Y, Miyamoto T, Shiota H, Keshavarz P, Yamaguchi Y, Kunika K, Moritani M, Inoue H, Itakura M: Association study on chromosome 20q11.21-13.13 locus and its contribution to type 2 diabetes susceptibility in Japanese. Hum Genet 2006;120:527-542.

  5. Moritani M, Togawa K, Yaguchi H, Fujita Y, Yamaguchi Y, Inoue H, Kamatani N, Itakura M: Identification of diabetes susceptibility loci in db mice by combined quantitative trait loci analysis and haplotype mapping. Genomics 2006;88(6):719-730.

  6. Keshavarz P, Inoue H, Sakamoto Y, Kunika K, Tanahashi T, Nakamura N, Yoshikawa T, Yasui N, Shiota H, Itakura M: No evidence for association of the ENPP1 (PC-1) K121Q variant with risk of type 2 diabetes in a Japanese population. J Hum Genet 2006;51:559-566.

  7. Kato H, Nomura K, Osabe D, Shinohara S, Mizumori O, Katashima R, Iwasaki S, Nishimura K, Yoshino M, Kobori M, Ichiishi E, Nakamura N, Yoshikawa T, Tanahashi T, Keshavarz P; Kunika K, Moritani M, Kudo E, Tsugawa K; Takata Y, Hamada D, Yasui N, Miyamoto T, Shiota H, Itakura M: Association of Single-nucleotide Polymorphisms in the Suppressor of Cytokine Signaling 2 (SOCS2) Gene with Type 2 Diabetes (T2D) in Japanese. Genomics 2006;87:446-458.

  8. Togawa K, Moritani M, Yaguchi H, Itakura M: Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in mice. Hum Mol Genet 2006;15:15:113-128.

  9. Takata Y, Matsui Y, Hamada D, Goto T, Kubo T, Egawa H, Nakano S, Shinomiya F, Inoue H, Itakura M, Yasui N: The alpha 2 type IX collagen gene tryptophan polymorphism is not associated with rheumatoid arthritis in the Japanese population. Clin Rheumatol 2006:25:491-494.

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2005

  1. Itoh Y, Mizuki N, Shimada T, Azuma F, Itakura M, Kashiwase K, Kikkawa E, Kulski JK, Satake M, Inoko H: High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population. Immunogenetics 2005;57:717-729.

  2. Ogawa T, Nikawa T, Furochi H, Kosyoji M, Hirasaka K, Suzue N, Sairyo K, Nakano S, Yamaoka T, Itakura M, Kishi K, Yasui N: Osteoactivin upregulates expression of MMP-3 and MMP-9 in fibroblasts infiltrated into denervated skeletal muscle in mice. Am J Physiol Cell Physiol 2005;289:C697-707.

  3. Endo Y, Zhang L, Katashima R, Itakura M, Doherty EA, Barron AE, Baba Y: Effect of polymer matrix and glycerol on rapid single-strand conformation polymorphism analysis by capillary and microchip electrophoresis for detection of mutations in K-ras gene. Electrophoresis 2005;26:3380-3386.

  4. Yaguchi H, Togawa K, Moritani M, Itakura M: Identification of candidate genes in the type 2 diabetes modifier locus using expression QTL. Genomics 2005;85:591-599.

  5. Hamada D, Takata Y, Osabe D, Nomura K, Shinohara S, Egawa H, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Miyamoto T, Moritani M, Kunika K, Inoue H, Yasui N, Itakura M: Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population. Arthritis Rheum 2005;52:1371-1380.

  6. Ohuchi H, Yasue A, Ono K, Sasaoka S, Tomonari S, Takagi A, Itakura M, Moriyama K, Noji S, Nohno T: Identification of cis-element regulating expression of the mouse Fgf10 gene during inner ear development Dev Dyn 2005;233:177-187.

  7. Tsutsumi S, Inoue H, Sakamoto Y, Mizuta K, Kamata N, Itakura M: Molecular cloning and characterization of the murine gnathodiaphyseal dysplasia gene GDD1. Biochem Biophys Res Commun 2005;331:1099-1106.

  8. Moritani M, Yamasaki S, Kagami M, Suzuki T, Yamaoka T, Sano T, Hata J, Itakura M: Hypoplasia of endocrine and exocrine pancreas in homozygous transgenic TGF-beta1. Mol Cell Endocrinol 2005;229:175-184.

  9. Miyamoto T, Inoue H, Sakamoto Y, Kudo E, Naito T, Mikawa T, Mikawa Y, Isashiki Y, Osabe D, Shinohara S, Shiota H, Itakura M: Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome. Invest Ophthalmol Vis Sci 2005;46:2726-2735.

  10. De La Vega FM, Isaac H, Collins A, Scafe CR, Halldorsson BV, Su X, Lippert RA, Wang Y, Laig-Webster M, Koehler RT, Ziegle JS, Wogan LT, Stevens JF, Leinen KM, Olson SJ, Guegler KJ, You X, Xu LH, Hemken HG, Kalush F, Itakura M, Zheng Y, de The G, O'Brien SJ, Clark AG, Istrail S, Hunkapiller MW, Spier EG, Gilbert DA: The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern. Genome Res 2005;15:454-462.

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2004

  1. Hino S, Yamaoka T, Yamashita Y, Yamada T, Hata J, Itakura M: In vivo proliferation of differentiated pancreatic islet beta cells in transgenic mice expressing mutated cyclin-dependent kinase 4. Diabetologia 2004;47:1819-1830.

  2. Kudo E, Kamatani N, Tezuka O, Taniguchi A, Yamanaka H, Yabe S, Osabe D, Shinohara S, Nomura K, Segawa M, Miyamoto T, Moritani M, Kunika K, Itakura M: Familial juvenile hyperuricemic nephropathy: detection of mutations in the uromodulin gene in five Japanese families. Kidney Int 2004;65:1589-1597.

  3. Ii S, Ohta M, Kudo E, Yamaoka T, Tachikawa T, Moritani M, Itakura M, Yoshimoto K: Redox state-dependent and sorbitol accumulation-independent diabetic albuminuria in mice with transgene-derived human aldose reductase and sorbitol dehydrogenase deficiency. Diabetologia 2004;47:541-548.

  4. Tsutsumi S, Kamata N, Vokes TJ, Maruoka Y, Nakakuki K, Enomoto S, Omura K, Amagasa T, Nagayama M, Saito-Ohara F, Inazawa J, Moritani M, Yamaoka T, Inoue H, Itakura M: The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD). Am J Hum Genet 2004;74:1255-1261.

  5. Hwang YC, Kaneko M, Bakr S, Liao H, Lu Y, Lewis ER, Yan S, Ii S, Itakura M, Rui L, Skopicki H, Homma S, Schmidt AM, Oates PJ, Szabolcs M, Ramasamy R: Central role for aldose reductase pathway in myocardial ischemic injury. Faseb J 2004;18:1192-1199.

  6. Mizusawa N, Hasegawa T, Ohigashi I, Tanaka-Kosugi C, Harada N, Itakura M, Yoshimoto K: Differentiation phenotypes of pancreatic islet beta- and alpha-cells are closely related with homeotic genes and a group of differentially expressed genes. Gene 2004;331:53-63.

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2003

  1. Kitabayashi M, Nishiya Y, Esaka M, Itakura M, Imanaka T: Gene cloning and function analysis of replication factor C from Thermococcus kodakaraensis KOD1. Biosci Biotechnol Biochem 2003;67:2373-2380.

  2. Tsutsumi S, Kamata N, Maruoka Y, Ando M, Tezuka O, Enomoto S, Omura K, Nagayama M, Kudo E, Moritani M, Yamaoka T, Itakura M: Autosomal dominant gnathodiaphyseal dysplasia maps to chromosome 11p14.3-15.1. J Bone Miner Res 2003;18:413-418.

  3. Honda S, Tanaka-Kosugi C, Yamada S, Sano T, Matsumoto T, Itakura M, Yoshimoto K: Human pituitary adenomas infrequently contain inactivation of retinoblastoma 1 gene and activation of cyclin dependent kinase 4 gene. Endocr J 2003;50:309-318.

  4. Yamasaki H, Mizusawa N, Nagahiro S, Yamada S, Sano T, Itakura M, Yoshimoto K: GH-secreting pituitary adenomas infrequently contain inactivating mutations of PRKAR1A and LOH of 17q23-24. Clin Endocrinol (Oxf) 2003;58:464-470.

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2002

  1. Kitabayashi M, Nishiya Y, Esaka M, Itakura M, Imanaka T: Gene cloning and polymerase chain reaction with proliferating cell nuclear antigen from Thermococcus kodakaraensis KOD1. Biosci Biotechnol Biochem 2002;66:2194-2200.

  2. Yamaoka T, Yoshino K, Yamada T, Yano M, Matsui T, Yamaguchi T, Moritani M, Hata J, Noji S, Itakura M: Transgenic expression of FGF8 and FGF10 induces transdifferentiation of pancreatic islet cells into hepatocytes and exocrine cells. Biochem Biophys Res Commun 2002;292:138-143.

  3. Nishi M, Yasue A, Nishimatu S, Nohno T, Yamaoka T, Itakura M, Moriyama K, Ohuchi H, Noji S: A missense mutant myostatin causes hyperplasia without hypertrophy in the mouse muscle. Biochem Biophys Res Commun 2002;293:247-251.

  4. Ohno I, Ichida K, Okabe H, Moritani M, Itakura M, Saito M, Kamatani N, Hosoya T: Familial juvenile gouty nephropathy: exclusion of 16p12 from the candidate locus. Nephron 2002;92:573-575.

  5. Sasaki H, Yamaoka T, Ohuchi H, Yasue A, Nohno T, Kawano H, Kato S, Itakura M, Nagayama M, Noji S: Identification of cis-elements regulating expression of Fgf10 during limb development. Int J Dev Biol 2002;46:963-967.

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2001

  1. Yamaoka T, Yano M, Kondo M, Sasaki H, Hino S, Katashima R, Moritani M, Itakura M: Feedback inhibition of amidophosphoribosyltransferase regulates the rate of cell growth via purine nucleotide, DNA, and protein syntheses. J Biol Chem 2001;276:21285-21291.

2000

  1. Yamaoka T, Yoshino K, Yamada T, Idehara C, Hoque MO, Moritani M, Yoshimoto K, Hata J, Itakura M: Diabetes and tumor formation in transgenic mice expressing Reg I. Biochem Biophys Res Commun 2000;278:368-376.

  2. Takeuchi F, Kawasugi K, Nabeta H, Mori M, Moritani M, Goto M, Matsuta K, Yamada A, Chihara T, Hanyu T, Murayama T, Yamamoto S, Murata N, Matsubara T, Itakura M: HLA-DR shared epitope in familial cases of Japanese rheumatoid arthritis. Clin Exp Rheumatol 2000;18:423-424.

  3. Sasahara K, Yamaoka T, Moritani M, Tanaka M, Iwahana H, Yoshimoto K, Miyagawa J, Kuroda Y, Itakura M: Molecular cloning and expression analysis of a putative nuclear protein, SR-25. Biochem Biophys Res Commun 2000;269:444-450.

  4. Yamaoka T, Yano M, Yamada T, Matsushita T, Moritani M, Ii S, Yoshimoto K, Hata J, Itakura M: Diabetes and pancreatic tumours in transgenic mice expressing Pa x 6. Diabetologia 2000;43:332-339.

  5. Abe T, Yoshimoto K, Taniyama M, Hanakawa K, Izumiyama H, Itakura M, Matsumoto K: An unusual kindred of the multiple endocrine neoplasia type 1 (MEN1) in Japanese. J Clin Endocrinol Metab 2000;85:1327-1330.

  6. Kondo M, Yamaoka T, Honda S, Miwa Y, Katashima R, Moritani M, Yoshimoto K, Hayashi Y, Itakura M: The rate of cell growth is regulated by purine biosynthesis via ATP production and G(1) to S phase transition. J Biochem ( Tokyo ) 2000;128:57-64.

  7. Sasahara K, Yamaoka T, Moritani M, Yoshimoto K, Kuroda Y, Itakura M: Molecular cloning and tissue-specific expression of a new member of the regenerating protein family, islet neogenesis-associated protein-related protein. Biochim Biophys Acta 2000;1500:142-146.

  8. Kamatani N, Moritani M, Yamanaka H, Takeuchi F, Hosoya T, Itakura M: Localization of a gene for familial juvenile hyperuricemic nephropathy causing underexcretion-type gout to 16p12 by genome-wide linkage analysis of a large family. Arthritis Rheum 2000;43:925-929.

  9. Kikutsuji T, Harada M, Tashiro S, Ii S, Moritani M, Yamaoka T, Itakura M: Expression of somatostatin receptor subtypes and growth inhibition in human exocrine pancreatic cancers. J Hepatobiliary Pancreat Surg 2000;7:496-503.

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