Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

スポンサーリンク

概要

• 論文の詳細を見る
• Springer-Verlag Tokyoの論文
• 1999-01-01

著者

• Sasaki Ayako

  山形大学 医学部小児科学

• Sasaki Ayako

  Department Of Pediatrics Yamagata University School Of Medicine

• Kimura Toshiyuki

  Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Hokuriku University

• Yasumura Seiji

  Department of Public Health, Yamagata University School of Medicine

• HAYASAKA KIYOSHI

  Department of Pediatrics, Yamagata University School of Medicine

• Hiroi Masahiko

  Department Of Physics Kyoto University

• Hiroi Masahiko

  Department Of Obstetrics And Gynecology Yamagata University School Of Medicine

• Yasumura Seiji

  Department Of Public Health Yamagata University School Of Medicine

• AKABA Kazuhiro

  Department of Pediatrics, Yamagata University School of Medicine

• TANABE Saori

  Department of Pediatrics, Yamagata University School of Medicine

• WAKABAYASHI Takashi

  Department of Pediatrics, Yamagata University School of Medicine

• MAKI Kazuko

  Yamagata Prefectural Institute of Public Health

• AIKAWA Shogo

  Yamagata Prefectural Institute of Public Health

• Aikawa Shogo

  Yamagata Prefectural Public Health Laboratory

• Maki Kazuko

  Yamagata Prefectural Public Health Laboratory

• Akaba Kazuhiro

  Department Of Pediatrics Yamagata University School Of Medicine

• Wakabayashi Takashi

  Department Of Anatomy Nagoya City University Medical School

• Hayasaka K

  Department Of Pediatrics Yamagata University School Of Medicine

• Hayasaka Kiyoshi

  Department Of Pediatrics Yamagata University School Of Medicine

• Hayasaka Kiyoshi

  Departments Of Pediatrics Yamagata University School Of Medicine

• Hayasaka Kiyoshi

  Department Of Pediatrics Yamagata University Faculty Of Medicine

• Sasaki Ayako

  Department Of Biofunctional Science Faculty Of Agriculture And Life Science Hirosaki University

• Kimura Toshiyuki

  Department Of Hygienic Chemistry Faculty Of Pharmaceutical Sciences Hokuriku University

• Kimura Toshiyuki

  Department Of Pediatrics Yamagata University School Of Medicine

• Tanabe Saori

  Faculty Of Bioresources Mie University

• Tanabe Saori

  Department Of Pediatrics Nagai City General Hospital

• Yasumura Seiji

  Department Of Public Health Fukushima Medical University School Of Medicine

• Wakabayashi Takashi

  Department Of Pediatrics Yamagata University School Of Medicine

• Tanabe Saori

  Department Of Pediatrics Yamagata Prefectural And Sakata Municipal Hospital Organization

• HIROI MASAHIKO

  Department of Obstetrics and Gynecology Niigata University School of Medicine

• Tanabe Saori

  Department of International Development Engineering, Graduate School of Science and Engineering, Tokyo Institute of Technology

関連論文

• Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: rs17884724:A>C is associated with 7-alanine expansion
• Butyrylcholinesterase and Erythrocyte Sulfhydryl-dependent Enzyme Hydrolyze Gabexate in Human Blood
• Involvement of Human Blood Arylesterases and Liver Microsomal Carboxylesterases in Nafamostat Hydrolysis
• Hepatic Metabolism of Methyl Anthranilate and Methyl N-Methylanthranilate as Food Flavoring Agents in Relation to Allergenicity in the Guinea Pig
• In Vitro Inhibitory Effects of Cannabinoids on Progesterone 17α-Hydroxylase Activity in Rat Testis Microsomes
• Skin Reaction Induced by Aldehydes for Food Flavoring Agents
• Possible Existence of a Novel Receptor for Uridine Analogues in the Central Nervous System Using Two Isomers, N^3-(S)-(+)-and N^3-(R)-(-)-α-Hydroxy-β-phenethyluridines
• Cross-Reactivity of Various Tetrahydrocannabinol Metabolites with a Monoclonal Antibody against Tetrahydrocannabinolic Acid
• A Carbonyl Reductase-Catalyzing Reduction of N^3-Phenacyluridine in Rabbit Liver
• Synthesis and Pharmacological Evaluation in Mice of Halogenated Cannabidiol Derivatives
• Pharmacologica Efects in Mice of Anandamide and Its Related Fatty Acid Ethanolamides, and Enhancement of Cataleptogenic Effect of Anandamide by Phenylmethylsulfonyl Fluoride
• Synthesis and Pharmacological Activities in Mice of Halogenated Δ^9-Tetrahydrocannabinol Derivatives
• Early Mortality After Acute Myocardial Infarction : Observational Study in Yamagata, 1993-1995
• Genetic Analysis of Shwachman-Diamond Syndrome : Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
• Antiferro-Multipolar Short Range Order above the Antiferro-Quadrupolar Ordering Temperature in CeB_6
• Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese
• Frost Heaving Phenomena in Helium : I. QUANTUM LIQUIDS AND SOLIDS : He in Restricted Geometry
• Associated factors of rehospitalization among schizophrenic patients
• Separation of Flavonoids and Salt in Bean Cake Disposed from Soy Sauce Manufacturing Process
• Patterns of distribution of Ag-NORs in the genus Apodemus and their evolutionary implications
• The Pharmacokinetics of Low-Dose Thalidomide in Japanese Patients with Refractory Multiple Myeloma(Biopharmacy)
• Convenient Regioselective mono-2-O-Sulfonation of Cyclomaltooctaose
• Discrimination of Cooked Mochiminori and Koshihikari Rice Grains by Observation of Internal Hollows Using Light Transmittance Photography
• Compertitive Inhibition of Δ^8-Tetrahydrocannabinol and Its Active Metabolites for Cannabinoid Receptor Binding
• Anandamide, an Endogenous Cannabinoid Receptor Ligand, Also Interacts with 5-Hydroxytryptamine (5-HT) Receptor
• Human CD4^+ central and effector memory T cells produce IL-21 : effect on cytokine-driven proliferation of CD4^+ T cell subsets
• Synthesis and Hypnotic Activities of 4-Thio Analogues of N^3-Substituted Uridines
• Mutation analysis of phenylketonuria in Yamagata prefecture, Japan
• De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
• Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
• Congenital Central Hypoventilation Syndrome : A Novel Mutation of the RET Gene in an Isolated Case
• Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
• Modification of physicochemical properties of actin filaments suppresses cell fragmentation in the execution phase of staurosporine-induced apoptotic processes
• ultrastructural basis for the transition of cell death mode from apoptosis to necrosis in menadione-treated osteosarcoma 143B cells
• Functional aspects of megamitochondria isolated from hydrazine- and ethanol-treated rat livers
• Two types of the enlargement of mitochondria related to apoptosis: simple swelling and the formation of megamitochondria
• Prader-Willi syndrome in a child with XYY
• Mild immunoglobulin A nephropathy in a patient with a marked increase in serum immunoglobulin A
• Successful Unrelated Donor Bone Marrow Transplantation for Shwachman-Diamond Syndrome with Leukemia
• CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen
• Structural change of bovine retinal cGMP phosphodiesterase by release of its γ subunit : direct imaging by improved low angle rotary shadowing
• Periciliary structure of developing rat photoreceptor cells. A deep etch replica and freeze substitution study
• Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility
• A new form of total anomalous pulmonary venous connection with double drainage
• Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease
• Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
• Deletion and Nonsense Mutations of the Connexin 32 Gene Associated with Charcot-Marie-Tooth Disease
• Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor δ2 autoantibody
• A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor δ2
• STRUCTURE-ACTIVITY RELATIONSHIP OF URIDINE DERIVATIVES FOR HYPNOTIC ACTIVITY
• Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy
• Anisotropic Magnetic Phase Diagram of PrB_6 Dominated by the O_ Antiferro-Quadrupolar Interaction : Condensed Matter: Electronic Properties, etc.
• Relationship of Serum Lipids to 10-year Deaths from All Causes and Cancer in Japanese Urban Dwellers Aged 40 Years and Over
• Self-rated Health as a Predictor of Active Life in the Community Elderly
• Transport Properties in Phase IV of Ce_xLa_B_6 : Condensed Matter: Electronic Properties, etc.
• Beraprost sodium for pulmonary hypertension with congenital heart disease
• Management of Functional Pulmonary Atresia with Isoproterenol in a Neonate with Ebstein's Anomaly
• Microangiopathic Hemolytic Anemia and Thrombocytopenia in a Child with Atrial Septal Defect and Pulmonary Hypertension
• Expression of c-Mpl and c-Mpl ligand gene in hematopoietic cells of individuals with and without myeloproliferative disorders and leukemia cell lines
• THE EFFECT OF POLYANIONS AS NEGATIVE STAINS ON THE STRUCTURE OF OSMOTICALLY SENSITIVE MEMBRANE SYSTEMS : I. TUNGSTATE
• Changes in physicochemical properties of microtubules lead to the formation of a single spherical structure of mitochondrial assembly enveloping nuclear chromatins
• Role of mitochondria in the switch mechanism of the cell death mode from apoptosis to necrosis-Studies on ρ^0 cells
• Risk factors of scabies in psychiatric and long-term care hospitals : A nationwide mail-in survey in Japan
• Terminal deletion of chromosome 10q : Clinical features and literature review
• Effects of D-Penicillamine on the Induction of Pseudopregnancy by Copper in Rats and Rabbits
• Mechanism of Copper-Induced Ovulation by the Incubation Experiment of the Anterior Pituitary Gland
• THE EFFECT OF POLYANIONS AS NEGATIVE STAINS ON THE STRUCTURE OF OSMOTICALLY SENSITIVE MEMBRANE SYSTEMS : II MOLYBDATE
• ON THE FORMATION PROCESS AND BIOCHEMICAL PROPERTIES OF DIETHYLDITHIOCARBAMATE (DDC)-INDUCED MEGAMITOCHONDRIA : II. SOME BIOCHEMICAL PROPERTIES OF DDC-INDUCED MEGAMITOCHONDRIA
• ON THE FORMATION PROCESS AND BIOCHEMICAL PROPERTIES OF DIETHYLDITHIOCARBAMATE (DDC)-INDUCED MEGAMITOCHONDRIA : I. ULTRASTRUCTURAL CHANGES OF MOUSE HEPATOCYTES BY DDC
• An Acute Increase in Serum Prolactin Does Not Modify Gonadotropin Release in Female Rats
• Lack of Inhibitory Effect of Exogenous Prolactin on Ovarian Responsiveness to Gonadotropins in the Rat
• Maturation of Negative and Positive Estrogen Feedback in the Prepubertal Female Rat
• Prolactin Bioassay : Its Sensitivity and Stability
• A Case of Glycogen Storage Disease Type III (Glycogen Debranching Enzyme Deficiency) with Liver Cirrhosis and Hypertrophic Cardiomyopathy
• Lung Hypoplasia in Developing Mice and Rats Induced by Maternal Exposure to Nitrofen
• Comparison of the Perceptions of City Residents and Physicians Regarding "Good Death" in a Terminal Cancer Setting in Fukushima, Japan
• Perception of anesthesia safety and postoperative symptoms of surgery patients in Ho Chi Minh City, Vietnam : a pioneering trial of postoperative care assessment in a developing nation
• 日本での成熟児における下気道感染症と消化器感染症による入院
• A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1
• Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
• Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan
• An Elderly Japanese Patient with Adult-onset Type II Citrullinemia with a Novel D493G Mutation in the SLC25A13 Gene
• Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype
• Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion
• Risk factors for recurrence of scabies : A retrospective study of scabies patients in a long-term care hospital
• Phenotypic variability in a family with Townes-Brocks syndrome
• The GARS gene is rarely mutated in Japanese patients with Charcot-Marie-Tooth neuropathy
• Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
• Support-seeking behavior among Japanese mothers at high-risk of mental health problems: a community-based study at a city health center
• High-Field Magnetization Measurements of Fe
• Prevalence of and Factors Associated with Reproductive Tract Infections among Pregnant Women in Ten Communes in Nghe An Province, Vietnam
• Association of Pregnancy Intention with Parenting Difficulty in Fukushima, Japan
• Factors Relating to the Bone Mineral Density in the Elderly Living in the Urban Community
• Angioplasty but Not Thrombolysis Improves Short-term Mortality of Acute Myocardial Infarction. A Multicenter Survey in Yamagata, Japan.
• Magnetic and spectral properties of dimeric copper(II) phenylpropynoate complexes.
• Two newborn-onset patients of Upshaw-Schulman syndrome with distinct subsequent clinical courses
• Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children
• Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms : 211G>A (G71R) mutation becomes a risk factor under inadequate feeding
• A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy
• Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan

もっと見る 閉じる

スポンサーリンク