Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism

スポンサーリンク

概要

• 論文の詳細を見る
• 2004-01-01

著者

• Nanba Eiji

  Gene Research Center, Tottori University

• Nanba Eiji

  Division Of Functional Genomics Research Center For Bioscience And Technology Tottori University

• Nanba Eiji

  Gene Research Center Tottori University

• Nanba Eiji

  東京大学 医学系研究科精神神経科

• KATO Nobumasa

  Department of Psychiatry, Showa University School of Medicine

• Kato N

  Gumma Univ. School Of Medicine Gumma Jpn

• Kato Nobumasa

  Department Of Neuropsychiatry Faculty Of Medicine University Of Tokyo

• TOCHIGI Mamoru

  Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo

• KATO Chieko

  Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo

• HASHIMOTO Ohiko

  Department of Medical Technology, Aino University

• SASAKI Tsukasa

  Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo

• MARUI Tetsuya

  Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo

• UMEKAGE Tadashi

  Department of Psychiatry, Graduate School of Medicine, University of Tokyo

• Kato Nobumasa

  Department Of Psychiatry Faculty Of Medicine University Of Tokyo

• Kato Chieko

  Department Of Neuropsychiatry Graduate School Of Medicine University Of Tokyo

• Marui Tetsuya

  Department Of Neuropsychiatry Graduate School Of Medicine University Of Tokyo

• Sasaki Tsukasa

  Department Of Neuropsychiatry Graduate School Of Medicine University Of Tokyo

• Tochigi Mamoru

  Department Of Neuropsychiatry Graduate School Of Medicine University Of Tokyo

• Hashimoto Ohiko

  Department Of Medical Technology Aino University

• Kakiuchi Chihiro

  理化学研究所脳科学総合研究センター 精神疾患動態研究チーム

• Umekage Tadashi

  Department Of Psychiatry Health Service Center University Of Tokyo

• Umekage Tadashi

  Department Of Pharmacology National Defense Medical College

• Kato Chieko

  Department Of Materials Science Faculty Of Science Kanagawa University

• Kushino Nobuhisa

  Department Of Psychiatry School Of Medicine Showa University

• Sasaki Tsukasa

  Department Of Ergonomics Graduate School Of Science And Technologychiba University

• Umekage Tadashi

  Department Of Neuropsychiatry Graduate School Of Medicine University Of Tokyo

関連論文

• Developmental Changes of Ni^ Sensitivity and Automaticity in Nkx2.5-Positive Cardiac Precursor Cells From Murine Embryonic Stem Cell
• State-Dependent Blocking Actions of Azimilide Dihydrochloride (NE-10064) on Human Cardiac Na^+ Channels
• FRS-091 Impairment of Ubiquitin-Proteasome System Caused by a Missense MYBPC3 Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Sessi
• Congenital myotonic dystrophy : report of paternal transmission
• 1 Role of the Ubiquitin Proteasome System in the Development of Heart Failure in Hypertrophic Cardiomyopathy(Young Investigator's Award for International Students Finalists Lecture (YIA International),Special Program,The 72nd Annual Scientific Meeting of
• Subtype Switching of T-Type Ca^ Channels From Cav3.2 to Cav3.1 During Differentiation of Embryonic Stem Cells to Cardiac Cell Lineage
• Increased Plasma Urotensin-II and Carotid Atherosclerosis are Associated with Vascular Dementia
• Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouse
• No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population
• Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism : A case-control study
• Serotonin transporter gene promoter polymorphism and autism : A family-based genetic association study in Japanese population
• No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population
• Gastrin-releasing peptide receptor (GRPR) locus in Japanese subjects with autism
• Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin : A new syndrome?
• Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese
• Intracerebral cell transplantation therapy for murine GM1 gangliosidosis
• Association analysis of HSP90B1 with bipolar disorder
• Galactonojirimycin derivatives restore mutant human β-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse
• Increased NPC1 mRNA in skin fibroblasts from Niemann-Pick disease type C patients
• Novel TSC1 and TSC2 mutations in Japanese patients with tuberous sclerosis complex
• A novel interstitial deletion of KAL1 in a Japanese family with Kallmann syndrome
• Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome
• Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome
• Prevalence of post-traumatic stress disorder in incarcerated juvenile delinquents in Japan
• Absence of mutations in the β-catenin and adenomatous polyposis coli genes in papillary and follicular thyroid carcinomas
• Serum cholesterol, uric acid and cholinesterase in victims of the Tokyo subway sarin poisoning : A relation with post-traumatic stress disorder
• Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population
• Association study of the dysbindin (DTNBP1) gene in schizophrenia from the Japanese population
• Retrospective In Utero Exposure Assessment of PCBs Using Preserved Umbilical Cords and Its Application to Case-Control Comparison
• Early Crisis Intervention to Patients with Acute Stress Disorder in General Hospital
• What causes seasonality of birth in schizophrenia?
• A Cell Line Derived from Sphingomyelinosis Mouse Shows Alterations in Intracellular Cholesterol Metabolism Similar to Those in Type C Niemann-Pick Disease
• Multiple-time replicability of near-infrared spectroscopy recording during prefrontal activation task in healthy men
• Bone marrow transplantation in subjects with mental disorders
• Combined analysis of association between personality traits and three functional polymorphisms in the tyrosine hydroxylase, monoamine oxidase A, and catechol-O-methyltransferase genes
• Mitochondrial DNA sequence analysis of patients with 'atypical psychosis'
• Support for relationship between serum cholinesterase and post-traumatic stress disorder ; 5-year follow-ups of victims of the Tokyo subway sarin poisoning
• Post-traumatic stress disorder symptoms in victims of Tokyo subway attack : a 5-year follow-up study
• Executive and prefrontal dysfunction in unipolar depression : a review of neuropsychological and imaging evidence
• Effects of corollary discharge on event-related potentials during selective attention task in healthy men and women
• What causes seasonality of birth in schizophrenia?
• White matter hyperintensity detected by magnetic resonance imaging and lithium response in bipolar disorder : A preliminary observation
• Fibroblast screening for chaperone therapy in β-galactosidosis
• Psychological factors and survival after bone marrow transplantation in patients with leukemia
• Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
• Cytokines participate in neuronal death induced by trimethyltin in the rat hippocampus via type II glucocorticoid receptors
• A newly developed assay for melatonin using cells expressing human mel-1a receptor
• The Effects of Bright Light Exposure on Humans
• Comparing gene expression profiles in human liver, gastric, and pancreatic tissues using full-length-enriched cDNA libraries
• Fragile X carrier screening and FMR1 allele distribution in the Japanese population
• Liver chip and gene shaving
• ^I-IMP SPECTと^F-FDG PETによって診断しえた老年期うつ病の一例
• Running fit and geralized tonic-clonic seizure are differently controlled by differently subtypes receptors in the brain stem (vol. 2)
• Assessment of congenital nasal stenosis by shaded surface display reconstruction images
• Angiotensinogen Gene Variation and Hypertension in a Cohort Study in Japanese
• Reduced intracellular pH in the basal ganglia and whole brain measured by ^P-MRS in bipolar disorder
• Phosphorylation of Delta2 Glutamate Receptors at Serine 945 is Not Required for Cerebellar Long-term Depression
• Review of animal models for autism : implication of thyroid hormone
• Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
• A case of galactosialidosis with a homozygous Q49R point mutation
• Audiogenic seizure induces c-fos mRNA expression in the inferior colliculus and not in the hippocampus
• Molecular genetic studies of schizophrenia : challenges and insights
• Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn
• Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
• Increased expression of β-hexosaminidase α chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I
• Integration of a transposon into the Gli3 gene in the Pdn mouse
• Association of the XBP1-116C/G polymorphism with schizophrenia in the Japanese population
• Effects of creatine on mental fatigue and cerebral hemoglobin oxygenation
• Effects of sleep deprivation : The phosphorus metabolism in the human brain measured by ^P-magnetic resonance spectroscopy
• A search for a mutation in the tumour necrosis factor-alpha gene in narcolepsy
• Familial Paroxysmal Kinesigenic Choreoathetosis : An Electrophysiologic and Genotypic Analysis
• Neuroanatomy and neurophysiology in schizophrenia
• Angiotensinogen Gene Variation and Hypertension in a Cohort Study in Japanese
• Regulation of Cigarette Smoke-Induced Cytochrome P4501A1 Gene Expression in Osteogenic Disorder Shionogi Rat Liver and in Lung by Large Ascorbic Acid Dose(Biochemistry & Molecular Biology)
• Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria
• 小児肥満におけるβ_3アドレナリン受容体とメラノコルチン受容体の遺伝子解析
• Electrophysiological indices associated with social functioning outcome in schizophrenia : a 5-year follow-up study
• Neuropeptide Y and somatostatin participate differently in the seizure-generating mechanisms following trimethyltin-induced hippocampal damage
• Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
• Serum-Soluble c-Kit Levels During Mobilization of Peripheral Blood Stem Cells Correlate With Stem Cell Yield
• Beneficial effects of FK506 for experimental temporal lobe epilepsy
• Aberrant promoter methylation and expression of the imprinted PEG3 gene in glioma
• Temporospatial patterns of COX-2 expression and pyramidal cell degeneration in the rat hippocampus after trimethyltin administration
• ^I-IMP SPECTと^F-FDG PETによって診断しえた老年期うつ病の一例
• Genetic and neuroimaging studies in schizophrenia
• Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
• A genome-wide CNV association study on panic disorder in a Japanese population
• An association analysis of Per2 with panic disorder in the Japanese population
• Male Hatano High-Avoidance Rats Show High Avoidance and High Anxiety-Like Behaviors as Compared with Male Low-Avoidance Rats
• Novel Mutations in the Gene Encoding Acid .ALPHA.-1,4-glucosidase in a Patient with Late-onset Glycogen Storage Disease Type II (Pompe Disease) with Impaired Intelligence
• Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
• Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population
• No association between the brain-derived neurotrophic factor gene and panic disorder in Japanese population
• Replication of a genome-wide association study of panic disorder in a Japanese population
• Genome-wide association study of panic disorder in the Japanese population
• Male Hatano High-Avoidance Rats Show High Avoidance and High Anxiety-Like Behaviors as Compared with Male Low-Avoidance Rats
• Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the NEU1 Gene
• The Role of Parasympathetic Nervous System in Stress-Induced Gastric Ulcer Formation: A Comparative Study on SHR, WKY, Wistar and MSG (monosodium-L-glutamate)-Treated Rats
• Gene expression profiling of major depression and suicide in the prefrontal cortex of postmortem brains
• A Novel Mutation of the GAA Gene in a Patient with Adult-onset Pompe Disease Lacking a Disease-specific Pathology

もっと見る 閉じる

スポンサーリンク