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Genomes and Genes | Kentaro YamadaSummaryAffiliation: Kurume University School of Medicine Country: Japan Publications
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Publications
Codon 972 polymorphism of the insulin receptor substrate-1 gene in impaired glucose tolerance and late-onset NIDDMK Yamada
Department of Medicine, Kurume University School of Medicine, Kurume, Japan
Diabetes Care 21:753-6. 1998..To assess the relevance of a Gly-->Arg substitution in codon 972 of the insulin receptor substrate-1 gene in impaired glucose tolerance (IGT) and NIDDM...
Sequencing of the putative promoter region of the cocaine- and amphetamine-regulated-transcript gene and identification of polymorphic sites associated with obesityK Yamada
Department of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Japan
Int J Obes Relat Metab Disord 26:132-6. 2002..We tested the hypothesis that polymorphisms in the cocaine- and amphetamine-regulated-transcript (CART) gene is associated with the development of obesity...
Distinct pharmacodynamics of insulin glargine and insulin detemir: crossover comparison in Type 1 and Type 2 diabetic patients on basal-bolus regimenTomoko Kato
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka 830 0011 Japan
Diabetes Res Clin Pract 90:e64-6. 2010..Glargine showed lower post-dinner and bedtime glucose levels in Type 1 diabetes, and lower pre-dinner and post-dinner glucose levels in Type 2 diabetes than detemir...
Essential role of caspase-3 in apoptosis of mouse beta-cells transfected with human FasK Yamada
Department of Medicine, Kurume University School of Medicine, Japan
Diabetes 48:478-83. 1999..These observations suggest the essential role of caspase-3 in Fas-mediated apoptosis of the beta-cell line...
Effects of adiponectin transgenic expression in liver of nonalcoholic steatohepatitis model miceHitomi Nakayama
Department of Medicine, Division of Endocrinology and Metabolism, Kurume University, Kurume, Fukuoka, Japan
Metabolism 58:901-8. 2009..These observations suggest that hypoadiponectinemia plays a key role in the pathogenesis of NASH associated with insulin resistance and may provide a clue to the novel therapy for human NASH...
Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese populationMichiko Ichimura
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan
Thyroid 18:625-30. 2008..The objective of this study was to investigate whether PTPN22 gene polymorphisms confer susceptibility to GD and Graves' ophthalmopathy (GO) in a Japanese population...
Clinical and genetic features of childhood-onset Type 2 diabetes in JapanShuichi Otabe
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume, Japan
Acta Diabetol 44:181-5. 2007..This suggests that malfunction of pancreatic beta-cells triggers hyperglycemia resulting in the requirement for insulin in Japanese some childhood-onset T2DM patients...
Interleukin-12B gene polymorphism does not confer susceptibility to Graves' ophthalmopathy in Japanese populationYuji Hiromatsu
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan
Endocr J 53:753-9. 2006..In conclusion, IL-12B gene 1188A/C polymorphism is not associated with GD or GO susceptibility in Japanese...
Excessive maternal transmission of diabetes in Japanese families with young-onset type 2 diabetes and insulin secretion defect according to clinical featuresShuichi Otabe
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, 67 Asahi Machi, Kurume, Fukuoka 830 0011, Japan
Acta Diabetol 47:133-8. 2010..0.50 ± 0.19 nmol/l, respectively. These results demonstrated that YT2D among Japanese people occurring in excess with maternal transmission is associated with β-cell dysfunction at the onset of diabetes and as the disease advances...
Overexpression of human adiponectin in transgenic mice results in suppression of fat accumulation and prevention of premature death by high-calorie dietShuichi Otabe
Department of Medicine, Kurume University School of Medicine, 67 Asahimachi, Kurume, Fukuoka 830 0011, Japan
Am J Physiol Endocrinol Metab 293:E210-8. 2007..These observations may provide new insights into the prevention and therapy of metabolic syndrome in humans...
Epigallocatechin-3-gallate improves nonalcoholic steatohepatitis model mice expressing nuclear sterol regulatory element binding protein-1c in adipose tissueTakato Ueno
Research Center for Innovative Cancer Therapy, Kurume University, Kurume, 830 0011, Japan
Int J Mol Med 24:17-22. 2009..From these results, EGCG reduces inflammation, insulin resistance and oxidative stress, and suppresses liver injury in nSREBP-1c transgenic mice...
A C/T polymorphism in the 5' untranslated region of the CD40 gene is associated with later onset of Graves' disease in JapaneseTokunori Mukai
Department of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume, Fukuoka
Endocr J 52:471-7. 2005..These data suggest that the SNP of CD40 gene is associated with susceptibility to later onset of GD in Japanese...
Transgenic mice expressing nuclear sterol regulatory element-binding protein 1c in adipose tissue exhibit liver histology similar to nonalcoholic steatohepatitisHitomi Nakayama
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume 830 0011, Japan
Metabolism 56:470-5. 2007..Thus, the nSREBP-1c transgenic mouse may serve as a unique model of spontaneously occurring NASH...
Plasma levels of n-decanoyl ghrelin, another acyl- and active-form of ghrelin, in human subjects and the effect of glucose- or meal-ingestion on its dynamicsJunko Yoh
Department of Physiology, Kurume University School of Medicine, Kurume, 830 0011 Fukuoka, Japan
Regul Pept 167:140-8. 2011....
Reduction of skeletal muscle, especially in lower limbs, in Japanese type 2 diabetic patients with insulin resistance and cardiovascular risk factorsYuji Tajiri
Endocrinology and Metabolism Division, Kurume University School of Medicine, Kurume, Japan
Metab Syndr Relat Disord 8:137-42. 2010..The aim of the present study was to evaluate characteristics of body composition in Japanese patients with type 2 diabetes...
Modulation by adiponectin of circadian clock rhythmicity in model mice for metabolic syndromeToshihiko Hashinaga
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume 830 0011, Japan
Endocr J 60:483-92. 2013..These results suggest that adiponectin is a peripheral regulator of the circadian clocks in the brain and peripheral organs, and may be a novel target for the treatment of obesity-associated disorders of circadian rhythms...
Long-term efficacy of sitagliptin for the treatment of type 2 diabetic patients in JapanYuji Tajiri
Division of Endocrinology and Metabolism, Kurume University School of Medicine, Kurume 830 0011, Japan
Endocr J 59:197-204. 2012....
Hyperadiponectinemia enhances bone formation in miceYasuhiro Mitsui
Department of Orthopedic Surgery, Kurume University, Kurume, Fukuoka, Japan
BMC Musculoskelet Disord 12:18. 2011..There is growing evidence that adiponectin, a physiologically active polypeptide secreted by adipocytes, controls not only adipose tissue but also bone metabolism. However, a role for adiponectin in bone development remains controversial...
[Soft drink ketosis]Kentaro Yamada
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine
Nippon Rinsho . 2006
Sequential activation of caspases and synergistic beta-cell cytotoxicity by palmitate and anti-Fas antibodiesNaotoshi Hirota
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, 67 Asahimachi, Kurume, 830-0011, Japan
Life Sci 79:1312-6. 2006..Fas-mediated beta-cell death and lipotoxicity may share common mechanisms involving caspase activation, and thereby synergistically inducing beta-cell death, although upstream signaling pathways are distinct...
Classification and characteristics of interferon-related diabetes mellitus in JapanKazuhisa Muraishi
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine Inada Naika Clinic, Kurume, Japan
Hepatol Res 41:184-8. 2011..The combined measurement of GAD antibody and HLA-typing could be an effective strategy to predict the onset of type 1 diabetes associated with IFN therapy...
Clinical characteristics of thyroid abnormalities induced by sunitinib treatment in Japanese patients with renal cell carcinomaShuichi Sato
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan
Endocr J 57:873-80. 2010..Therefore, thyroid function should be monitored in all patients treated with sunitinib...
Autoimmune hypophysitis treated with intravenous glucocorticoid therapyIkuyo Miyake
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine
Intern Med 45:1249-52. 2006..Early initiation of an intravenous dose of glucocorticoid followed by oral steroid administration therefore seems to be an efficient treatment for autoimmune hypophysitis even in patients with visual dysfunction...
IL-18 gene polymorphism confers susceptibility to the development of anti-GAD65 antibody in Graves' diseaseY Hiromatsu
Department of Endocrinology and Metabolism, Kurume University School of Medicine, Fukuoka, Japan
Diabet Med 23:211-5. 2006....
[A case of Cushing syndrome presenting after pulmonary nocardiosis with pyothorax]Tomoaki Hoshino
Division of Respirology, Neurology, and Rheumatology, Department of Medicine, Kurume University School of Medicine
Nihon Kokyuki Gakkai Zasshi 47:746-50. 2009..We assume that the present patient had pre-(sub-) clinical Cushing syndrome when she presented with pulmonary nocardiosis and pyothorax...
[Pharmacological treatment of postprandial hyperglycemia in hypertensive patients with type 2 diabetes mellitus]Kentaro Yamada
Department of Endocrinology and Metabolism, Kurume University School of Medicine
Nippon Rinsho 61:1219-23. 2003..These drugs may protect pancreatic beta-cells from postprandial glucose toxicity and prevent the progression of diabetes...
Mouse islet cell lysis mediated by interleukin-1-induced FasK Yamada
Department of Medicine, Kurume University School of Medicine, Japan
Diabetologia 39:1306-12. 1996..beta-TC1 cells also expressed Fas mRNA when exposed to IL-1 alpha or IL-1 alpha plus interferon-gamma. These observations suggest that Fas-mediated apoptosis may be a mechanism of islet cell death in autoimmune insulitis...
Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese menK Yamada
Department of Medicine, Kurume University School of Medicine, Japan
Diabetologia 40:706-10. 1997....
Metabolic clearance rate is a more robust and physiological parameter for insulin sensitivity than glucose infusion rate in the isoglycemic glucose clamp techniqueYuji Tajiri
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume, Japan
Diabetes Technol Ther 13:1057-61. 2011..The metabolic clearance rate (MCR) of glucose has been defined as the value of the glucose infusion rate (GIR) divided by the glucose concentration and could be thus expected to be a robust marker at various glucose concentrations...
A polymorphism of interferon-gamma gene associated with changes of anti-thyrotropin receptor antibodies induced by antithyroid drug treatment for Graves' disease in Japanese patientsTomoka Fukutani
Department of Endocrinology and Metabolism, Kurame University School of Medicine, Kurame, Japan
Thyroid 14:93-7. 2004..In conclusions, the CA repeat polymorphism of the IFN-gamma gene might be associated with the outcome of anti-thyroid drug treatment...
Serum level of free fatty acids is associated with nocturnal hypoglycemia in cirrhotic patients with HCV infection: a pilot studyTakumi Kawaguchi
Department of Digestive Disease Information and Research, Kurume University School of Medicine, Kurume 830 0011, Japan
Hepatogastroenterology 58:103-8. 2011..The aim of this study is to investigate a clinical parameter associated with nocturnal hypoglycemia in patients with hepatitis C virus (HCV)-related compensated liver cirrhosis...
Identification of hepatocyte growth factor activator (Hgfac) gene as a target of HNF1α in mouse β-cellsTsuyoshi Ohki
Department of Medical Biochemistry, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan
Biochem Biophys Res Commun 425:619-24. 2012..It has been reported that HGF has an important influence on β-cell mass and β-cell function. Thus, HNF1α might regulate β-cell mass or function at least partly by modulating Hgfac expression...
Relationship between clinicopathological factors and fluorine-18-fluorodeoxyglucose uptake in patients with papillary thyroid cancerHayato Kaida
Division of Nuclear Medicine, PET Center, Department of Radiology, Kurume University School of Medicine, Kurume City, Fukuoka, Japan
Nucl Med Commun 32:690-8. 2011..To examine the relationship between clinicopathological factors and fluorine-18-fluorodeoxyglucose (F-FDG) uptake in patients with papillary thyroid cancer (PTC)...
Pulmonary inflammation and emphysema: role of the cytokines IL-18 and IL-13Tomoaki Hoshino
Department of Internal Medicine 1, Kurume University School of Medicine, Kurume, Japan
Am J Respir Crit Care Med 176:49-62. 2007..Our results demonstrate that IL-18 overproduction in the lungs can induce lung diseases, such as pulmonary inflammation, lung fibrosis, and COPD...
Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathyS Amano
Division of Endocrinology and Metabolism, Department of Medicine, Kurume University School of Medicine, Kurume, Japan
Med Hypotheses 60:550-1. 2003..In this paper, we propose a novel hypothesis that polymorphisms of SDH gene may be correlated with SDH gene expression levels in diabetic retinas, thus being a valuable genetic marker for diabetic retinopathy...
Possible contribution of adipocytokines on diabetic neuropathyM Matsuda
Diabetes and Endocrine Division, Department of Medicine, Kawasaki Medical School, 577 Matsushima, Kurashiki shi, Okayama ken 701 0192, Japan
Diabetes Res Clin Pract 66:S121-3. 2004..The present results suggest that adipocytokines may play a role not only on angiopathy but also on neuropathy in diabetics...
Endogenous tumor necrosis factor-alpha production by a pancreatic beta-cell line: inhibitory effects of hydrocortisone and nicotinamideK Yamada
Department of Medicine, Kurume University School of Medicine, Japan
Life Sci 59:1423-9. 1996..These observations support the potential therapeutic role of glucocorticoids and nicotinamide in protecting beta-cells against cytokine-mediated damage, although glucocorticoid agonists have hyperglycemic metabolic effects...
Association between serotonin 4 receptor gene polymorphisms and bipolar disorder in Japanese case-control samples and the NIMH Genetics Initiative Bipolar PedigreesT Ohtsuki
Department of Medical Genetics, Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan
Mol Psychiatry 7:954-61. 2002..These findings suggest that genomic variations in the HTR4 gene may confer susceptibility to mood disorder...
No association of two missense variations of the benzodiazepine receptor (peripheral) gene and mood disorders in a Japanese sampleA Kurumaji
Department of Neuropsychiatry, Tokyo Medical and Dental University School of Medicine, Tokyo, Japan
Am J Med Genet 105:172-5. 2001..46-0.86). These results do not suggest that the BZRP gene plays a role in the genetic predisposition of affective disorders...
An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12K Yamada
Department of Human Genetics, Nagasaki University School of Medicine, Japan
Eur J Hum Genet 8:535-9. 2000..The mapping of the CPP3 locus to 20p12-q12 not only expands our understanding of the genetic heterogeneity in autosomal dominant posterior polar cataracts but also is a clue for the positional cloning of the disease gene...
A possible association of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma2 gene with obesity in native Javanese in IndonesiaC W Danawati
Division of Internal and Geriatric Medicine, Department of Development and Aging, Faculty of Medical Science, Kobe University Graduate School of Medicine, Japan
Diabetes Metab Res Rev 21:465-9. 2005..Among native Javanese ethnicity, however, there is no report about this polymorphism...
Sequence analysis of candidate genes for common susceptibility to type 1 and type 2 diabetes in miceK Yamada
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Japan
Endocr J 48:241-7. 2001..The coding sequence of Txn was identical in the three strains. These data suggest that neither of the two genes is a common susceptiblity gene between type 1 and type 2 diabetes in mice...
Identification of a compound short tandem repeat stretch in the 5'-upstream region of the cholecystokinin gene, and its association with panic disorder but not with schizophreniaE Hattori
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Wako, Saitama 351 0198, Japan
Mol Psychiatry 6:465-70. 2001..0003). These findings suggest that the novel STR or a nearby variant may confer susceptibility to the development of panic disorder...
An efficient linkage analysis strategy for autosomal dominant polycystic kidney diseaseT Onoe
Second Department of Internal Medicine, Kanazawa University School of Medicine, Ishikawa, Japan
Clin Nephrol 59:406-14. 2003..CONCLUSIONS: Automated genotyping using microsatellite markers, D16S3024, D16S3082, D16S3027 and D16S423 are very useful in the linkage analysis of ADPKD...
Family-based association study of schizophrenia with 444 markers and analysis of a new susceptibility locus mapped to 11q13.3K Yamada
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Saitama, Japan
Am J Med Genet B Neuropsychiatr Genet 127:11-9. 2004..In addition, we provide useful information on genomic LD structures in Japanese populations, which can be used for LD mapping of complex diseases...
Genetic polymorphisms and antiviral activity in the bovine MX1 geneY Nakatsu
Graduate School of Agriculture, Hokkaido University, Sapporo, Japan
Anim Genet 35:182-7. 2004..These results indicate that the bovine MX1 protein has potent antiviral activity...
Bone marrow transplantation from alpha1,3-galactosyltransferase gene-knockout pigs in baboonsY-L Tseng
Transplantation Biology Research Center, Massachusetts General Hospital/Harvard Medical School, Boston, MA 02129, USA
Xenotransplantation 11:361-70. 2004..In addition, cellular hyporesponsiveness was prolonged. However, long-term engraftment and chimerism were not achieved...
Mutations in the hypoxanthine guanine phosphoribosyltransferase gene (HPRT1) in Asian HPRT deficient familiesY Yamada
Department of Genetics, Inst Developmental Res, Aichi Human Service Center, Aichi, Japan
Nucleosides Nucleotides Nucleic Acids 23:1169-72. 2004....
[Schizophrenia and ocular misalignment: phenotypic and genetic association analysis]Y Yoshikawa
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute
Seishin Shinkeigaku Zasshi 106:1585-92. 2004..This study also highlights the unique nature of the polyalanine length variations found in PMX2B...
Gene expression and association analyses of LIM (PDLIM5) in bipolar disorder and schizophreniaT Kato
Laboratory for Molecular Dynamics of Mental Disorders, RIKEN Brain Science Institute, Wako Shi, Saitama, Japan
Mol Psychiatry 10:1045-55. 2005..No association was observed in case-control analysis and family-based association analysis in schizophrenia. These results suggest that SNPs in the upstream region of LIM may confer the genetic risk for bipolar disorder...
Genome-wide profiling of promoter methylation in humanI Hatada
Laboratory of Genome Science, Biosignal Genome Resource Center, Department of Molecular and Cellular Biology, Gunma University, Maebashi, Japan
Oncogene 25:3059-64. 2006..Genome-wide analysis of hypomethylated promoter sequences in cancer demonstrated low CG/GC ratio of these sequences, suggesting that CpG-poor genes are sensitive to demethylation activity in cancer...
Bovine and water buffalo Mx2 genes: polymorphism and antiviral activityH A E Babiker
Graduate School of Agriculture, Hokkaido University, Sapporo 060 8589, Japan
Immunogenetics 59:59-67. 2007..The positive control and all cells expressing Mx2 mRNAs displayed significantly higher levels of antiviral activity against VSVDeltaG*-G (P < 0.01) than did the negative controls...
Mice lacking bombesin receptor subtype-3 develop metabolic defects and obesityH Ohki-Hamazaki
Department of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan
Nature 390:165-9. 1997..BRS-3-deficient mice provide a useful new model for the investigation of human obesity and associated diseases...
Two-step association analyses of the chromosome 18p11.2 region in schizophrenia detect a locus encompassing C18orf1M Kikuchi
Mol Psychiatry 8:467-9. 2003
Biochemical and molecular genetic analyses on placental aromatase (P-450AROM) deficiencyN Harada
Division of Molecular Genetics, Fujita Health University, Aichi, Japan
J Biol Chem 267:4781-5. 1992..During the transient expression in COS-7 cells, the aromatase cDNA of the patient was found to produce a protein with a trace of activity. This is the first report of a genetic defect for aromatase deficiency...
Hyperresponsiveness to palatable and aversive taste stimuli in genetically obese (bombesin receptor subtype-3-deficient) miceK Yamada
Department of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira City, Tokyo, Japan
Physiol Behav 66:863-7. 1999..These results suggest that expression of the BRS-3 gene in these nuclei is important for the modulation of taste preference, as well as the development of obesity...
Vacuolar processing enzyme is up-regulated in the lytic vacuoles of vegetative tissues during senescence and under various stressed conditionsT Kinoshita
Department of Cell Biology, National Institute for Basic Biology, Okazaki, Japan
Plant J 19:43-53. 1999..Taken together, the results suggest that vegetative VPE might regulate the activation of some functional proteins in the lytic vacuoles...
Human ZHX1: cloning, chromosomal location, and interaction with transcription factor NF-YK Yamada
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, 707 Light Hall, Nashville, Tennessee, 37232 0615, USA
Biochem Biophys Res Commun 261:614-21. 1999..Both transcripts were expressed ubiquitously, although the 5-kilobase transcript is of greater abundance in most tissues examined. The human ZHX1 gene is located on chromosome 8q, between markers CHCL.GATA50B06 and CHLC. GATA7G07...
Schizosaccharomyces pombe homologue of glutathione peroxidase, which does not contain selenocysteine, is induced by several stresses and works as an antioxidantK Yamada
Institute for Developmental Research, Aichi Human Service Center, 713 8 Kamiya cho, Kasugai, Aichi 480 0392, Japan
Yeast 15:1125-32. 1999..The catalase gene disruptant of S. pombe harbouring multicopy plasmid containing gpx1(+) restored the hypersensitivity to H(2)O(2) of the catalase gene disruptant. These results suggest that Gpx1 acts as a scavenger of H(2)O(2) in vivo...
Cloning and expression of pleckstrin 2, a novel member of the pleckstrin familyT Inazu
Department of Biochemistry, Fukui Medical University, Matsuoka, Fukui, 910 1193, Japan
Biochem Biophys Res Commun 265:87-93. 1999..Distributions of N-terminal and C-terminal PH domains of pleckstrin 2 were quite different from each other, suggesting that these PH domains may interact with distinct factor(s)...
Differential effects of social isolation upon body weight, food consumption, and responsiveness to novel and social environment in bombesin receptor subtype-3 (BRS-3) deficient miceK Yamada
Department of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4 1 1 Ogawahigashi, Kodaira, Tokyo, Japan
Physiol Behav 68:555-61. 2000..These results suggest that BRS-3 expression in the CNS may affect the neural mechanisms that regulate isolation effects in wild-type animals...
Mutational analysis of the functional motifs of RuvB, an AAA+ class helicase and motor protein for holliday junction branch migrationH Iwasaki
Department of Molecular Microbiology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565 0871, Japan
Mol Microbiol 36:528-38. 2000....
Domain-specific mutations in TGFB1 result in Camurati-Engelmann diseaseA Kinoshita
Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki, Japan
Nat Genet 26:19-20. 2000..1-q13.3, which two other groups confirmed. As the human transforming growth factor-1 gene (TGFB1) is located within this interval, we considered it a candidate gene for CED...
Effects of kainate-mediated excitotoxicity on the expression of rat counterparts of A170 and MSP23 stress proteins in the brainK Nakaso
Department of Biochemistry, Faculty of Medicine, Tottori University, Yonago, Japan
Brain Res Mol Brain Res 69:155-63. 1999..These results suggest that A170 may play a protective role in the brain under kainate-mediated excitotoxicity...
Glutamate transporter GLT-1 is transiently localized on growing axons of the mouse spinal cord before establishing astrocytic expressionK Yamada
Department of Anatomy, Hokkaido University School of Medicine, Sapporo 060 8638, Japan
J Neurosci 18:5706-13. 1998....
Expression of local hepatocyte growth factor system in vascular tissuesY Nakamura
Department of Geriatric Medicine, Osaka University Medical School, Japan
Biochem Biophys Res Commun 215:483-8. 1995..Since HGF has characteristics of an endothelium-specific growth factor, locally synthesized HGF in endothelial cells and VSMC may have a role in vascular functions in autocrine-paracrine manner...
Expression of the human cGMP-dependent protein kinase II gene is lost upon introduction of SV40 T antigen or immortalization in human cellsM Fujii
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan
FEBS Lett 375:263-7. 1995..Also in various immortalized cell lines tested, the gene was not expressed. In normal diploid fibroblasts, the gene was constitutively expressed during cell-cycle and population doubling levels (PDLs)...
Targeted disruption of the tyrosine hydroxylase locus results in severe catecholamine depletion and perinatal lethality in miceK Kobayashi
Institute for Comprehensive Medical Science, School of Medicine, Fujita Health University, Aichi, Japan
J Biol Chem 270:27235-43. 1995..These results indicate that TH is essential for survival of the animals during the late gestational development and after birth...
Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridizationS Takai
Department of Genetics, International Medical Center of Japan, Tokyo
Hum Genet 95:96-8. 1995..We have mapped the human homolog (NEDD1) of the mouse gene to chromosome 12q22 by fluorescence in situ hybridization using R-banded human (pro)metaphase chromosomes...
Bcl-2 gene is highly expressed during neurogenesis in the central nervous systemS Abe-Dohmae
Department of Biochemistry, Nagoya City University Medical School, Japan
Biochem Biophys Res Commun 191:915-21. 1993..The results suggest that the bcl-2 gene functions to regulate development and survival of neurons in the central nervous system...
Chronic activation of protein kinase C in soleus muscles and other tissues of insulin-resistant type II diabetic Goto-Kakizaki (GK), obese/aged, and obese/Zucker rats. A mechanism for inhibiting glycogen synthesisA Avignon
J A Haley Veterans Hospital, Tampa, Florida 33612, USA
Diabetes 45:1396-404. 1996....
A novel brain-derived member of the epidermal growth factor family that interacts with ErbB3 and ErbB4S Higashiyama
Department of Biochemistry, Osaka University Medical School, Suita
J Biochem 122:675-80. 1997..Thus, NTAK appears to be a new member of the EGF family displaying neuregulin properties...
Plasminogen activator inhibitor-1 promoter 4G/5G genotype is not a risk factor for myocardial infarction in a Japanese populationT Sugano
The Second Department of Medicine, Kyoto Prefectural University of Medicine, Japan
Blood Coagul Fibrinolysis 9:201-4. 1998..This is in contrast to the first report in Caucasians, suggesting an interaction with other genetic or environmental factors which influences the risk of myocardial infarction...
Distinct expression of two types of Xenopus Patched genes during early embryogenesis and hindlimb developmentT Takabatake
Radioisotope Research Center, Nagoya University, Furo cho, Chikusa ku, 464 8602, Nagoya, Japan
Mech Dev 98:99-104. 2000..Despite the difference in their expression patterns, both are induced in animal cap explants synergistically by Shh and Noggin, showing a conserved regulation in their activation mechanisms...
Fluorescent quenching-based quantitative detection of specific DNA/RNA using a BODIPY((R)) FL-labeled probe or primerS Kurata
Kankyo Engineering Corporation, 1 Kimitsu, Kimitsu-shi, Chiba 299-1141, Japan
Nucleic Acids Res 29:E34. 2001..This widely applicable technique will be used directly with larger samples or in conjunction with the polymerase chain reaction to quantify small DNA samples...
Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samplesT Yoshikawa
Laboratory for Molecular Psychiatry, Brain Science Institute, RIKEN, Wako, Saitama 351 0198, Japan
Mol Psychiatry 6:202-10. 2001..Our findings suggest that IMPA2 or a gene nearby may contribute to the overall genetic risk for schizophrenia among Japanese...
Lack of association between hepatocyte nuclear factor-1beta gene and common forms of type 2 diabetes in the Japanese populationN Babaya
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Japan
Diabetes Nutr Metab 14:220-4. 2001..These results suggest that mutations in the HNF-1beta gene derived from a limited number of founders are not a major cause of common forms of Type 2 diabetes, even in the genetically homogeneous Japanese population...
Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductaseK Yamada
Biophysics Research Division and Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA
Proc Natl Acad Sci U S A 98:14853-8. 2001..D., et al. (1999) Nat. Struct. Biol. 6, 359-365]...
Lower mortality in patients with the DD genotype of the angiotensin-converting enzyme gene after acute myocardial infarctionS Tokunaga
Cardiovascular Center, Kansai Medical University, Moriguchi City, Osaka, Japan
Acta Cardiol 56:351-5. 2001..We assessed whether the ACE gene I/D polymorphism influenced cardiac mortality in Japanese patients with acute myocardial infarction...
Role of bombesin (BN)-like peptides/receptors in emotional behavior by comparison of three strains of BN-like peptide receptor knockout miceK Yamada
Department of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4 1 1 Ogawahigashi, Kodaira City, Tokyo 187 8502, Japan
Mol Psychiatry 7:113-7, 6. 2002..g., risk assessment behavior). Further, we found that the type of emotional behavior to which each of the peptide/receptor pathways contributes can be clearly specified...
Association studies of the CT repeat polymorphism in the 5' upstream region of the cholecystokinin B receptor gene with panic disorder and schizophrenia in Japanese subjectsE Hattori
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Wako, Saitama, Japan
Am J Med Genet 105:779-82. 2001....
Subchondral bone of the human knee joint in aging and osteoarthritisK Yamada
Department of Orthopaedics, University of California, San Diego, 9500 Gilman Dr. 0630, La Jolla 92093-0630, USA
Osteoarthritis Cartilage 10:360-9. 2002..Subchondral bone changes are not etiologic for OA but, more likely, are secondary to loss of articular cartilage which precedes the appearance of subchondral sclerosis...
Association analysis of adenylate cyclase type 9 gene using pedigree disequilibrium test in bipolar disorderT Toyota
Mol Psychiatry 7:450-2. 2002
Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patientsY Koda
Diabetologia 45:1039-40. 2002
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2M Nakano
Genetics, The Children s Hospital, Harvard Medical School, 300 Longwood Avenue, Enders 5, Boston, Massachusetts, USA
Nat Genet 29:315-20. 2001..These findings confirm the hypothesis that CFEOM2 results from the abnormal development of nIII/nIV (ref. 7) and emphasize a critical role for ARIX in the development of these midbrain motor nuclei...
Molecular cloning and functional characterization of chicken toll-like receptors. A single chicken toll covers multiple molecular patternsA Fukui
Department of Immunology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Nakamichi, Higashinari ku, Osaka 537 8511, Japan
J Biol Chem 276:47143-9. 2001..In oviparous animals, the duplicated TLRs in the pattern-recognition system may function for host-pathogen discrimination in a manner that is distinct from that in mammals...
Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrierK Yamada
Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki, Japan
Am J Med Genet 100:52-5. 2001..The unilateral blindness in the female carrier may have been due to non-random X-inactivation...
Isolation and characterization of vascular smooth muscle cell growth promoting factor from bovine ovarian follicular fluid and its cDNA cloning from bovine and human ovaryK Miyamoto
Department of Biochemistry, Fukui Medical University, Shimoaizuki, Matsuoka, Fukui 910 1193, Japan
Arch Biochem Biophys 390:93-100. 2001....
Alterations in the expression of the AQP family in cultured rat astrocytes during hypoxia and reoxygenationN Yamamoto
Department of Bioregulation Research, Nagoya City University Medical School, Mizuho-ku, 467-8601, Nagoya, Japan
Brain Res Mol Brain Res 90:26-38. 2001..These results suggest that AQP5 may be one of the candidates for inducing the intracranial edema in the CNS after ischemia injury...
Mapping and promoter sequencing of HNF-1beta gene in diabetes-prone and -resistant miceH Ueda
Department of Geriatric Medicine, Osaka University Medical School, 2 2 Yamadaoka, Suita, 565 0871, Osaka, Japan
Diabetes Res Clin Pract 53:67-71. 2001..3 cM)-Tcf2-(0.5 cM)-D11MIT195. A variant with insertion of C between -205 and -204 in the promoter region of Tcf2 was identified in NSY mice, but not NOD and C3H/He mice...
Polymorphism of CCR5 affecting HIV disease progression in the Japanese populationS Kageyama
Department of Virology, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930 0194, Japan
AIDS Res Hum Retroviruses 17:991-5. 2001..This indicates that the CCR5 genetic polymorphism affecting disease progression should be studied in a wider range of population...
Two types of HKT transporters with different properties of Na+ and K+ transport in Oryza sativaT Horie
Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0101, Japan
Plant J 27:129-38. 2001..These results suggest that two isoforms of HKT transporters, a Na+ transporter (OsHKT1) and a Na+- and K+-coupled transporter (OsHKT2), may act harmoniously in the salt tolerant indica rice...
Association studies of the cholecystokinin B receptor and A2a adenosine receptor genes in panic disorderK Yamada
Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Wako, Saitama, Japan
J Neural Transm 108:837-48. 2001..No evidence of association between the described variants and panic disorder was found. Our data therefore suggests that the CCKBR and A2aAR genes do not play major roles in the development of this disease...
Angiotensin-converting enzyme (ACE) I/D genotype and renal ACE gene expressionS Mizuiri
Department of Nephrology, Toho University, School of Medicine, Tokyo, Japan
Kidney Int 60:1124-30. 2001..We investigated a possible association between the ACE I/D genotype and renal ACE mRNA levels in healthy subjects...
N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complicationsH Pang
Diabet Med 20:419-20. 2003
