Characterization of Genes Encoding the Pancreatic β-cell ATP-sensitive K^+ Channel in Persistent Hyperinsulinemic Hypoglycemia of Infancy in Japanese Patients

スポンサーリンク

概要

• 論文の詳細を見る
• 2000-12-01

著者

• MIKI TAKASHI

  Department of Medicine, Yokohama Rosai Hospital

• SUGIHARA SHIGETAKA

  Department of Pediatrics, Tokyo Women's Medical University Daini Hospital

• Kohno Y

  Department Of Pediatrics Graduate School Of Medicine Chiba University:environmental Health Science P

• Kohno Yoichi

  国立病院機構千葉医療センター 小児科

• Kohno Yoichi

  Department Of Pediatrics Graduate School Of Medicine Chiba University

• Kohno Yoichi

  Department Of Pediatrics Chiba University Graduate School Of Medicine

• MINAGAWA MASANORI

  Department of Pediatrics, Chiba University Graduate School of Medicine

• Miki Takashi

  Department Of 2nd. Surgery Kurume Univ. School Of Medicine

• YASUDA Toshiyuki

  Department of Pediatrics, National Hospital Organization, Chiba Medical Center

• SOMEYA Tomohiro

  Department of Pediatrics, Graduate School of Medicine Chiba University

• SEINO Susumu

  Department of Molecular Medicine, Chiba University Graduate School of Medicine

• Tani Yoshiko

  Department Of Clinical Nutrition School Of Medicine Tokushima University

• Yasuda Toshiyuki

  Department Of Pediatrics School Of Medicine Chiba University

• Yasuda Toshiyuki

  Department Of Applied Chemistry Faculty Of Technology Tokyo University Of Agriculture And Technology

• Sugihara Shigetaka

  Department Of Pediatrics Chiba University School Of Medicine

• Miki T

  Department Of Molecular Medicine Chiba University Graduate School Of Medicine

• Kohno Yoichi

  Department Of Pediatrics Chiba University School Of Medicine

• Seino S

  Chiba Univ. Graduate School Of Medicine Chiba Jpn

• Seino Susumu

  Department Of Cellular And Molecular Medicine Graduate School Of Medicine Chiba University

• Taketani Yutaka

  Department Of Clinical Nutrition Institute Of Health Biosciences The University Of Tokushima

• Someya Tomohiro

  Department Of Pediatrics Graduate School Of Medicine Chiba University

• Someya Tomohiro

  Department Of Pediatrics Chiba University Graduate School Of Medicine

• Minagawa Masanori

  Department Of Pediatrics Chiba University Graduate School Of Medicine

• Minagawa Masanori

  Department Of Pediatrics Graduate School Of Medicine Chiba University

• Miki Takashi

  Department Of Medical Physiology Chiba University Graduate School Of Medicine

関連論文

• 日本人小児の Hemophilus influenzae type b 抗芙膜多糖体抗体価に関する検討
• Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome
• A novel KCNQ4 one-base deletion in a large pedigree with hearing loss : implication for the genotype-phenotype correlation
• Effect of Mazindol on Body Weight and Insulin Sensitivity in Severely Obese Patients after a Very-Low-Calorie Diet Therapy
• 小児1型糖尿病における超速効型インスリン使用の実態調査
• Association study of the C3 gene with adult and childhood asthma
• No Association of Polymorphisms in the 5' Region of the CD14 Gene and Food Allergy in a Japanese Population
• Effects of Probiotics on the Immune System and Allergic Diseases
• 6 Single nucleotide polymorphisms of CD14 and TLR2 is associated with the development of respiratory syncytial virus-induced bronchiolitis in Japanese children(II. Asthma Genetics)
• Increased expression of α4β7 integrin on food allergen-stimulated CD4^+ T cells in active food allergic enterocolitis
• Causes and Differential Diagnosis of Hypocalcemia : Recommendation Proposed by Expert Panel Supported by Ministry of Health, Labour and Welfare, Japan
• Threshold values of visceral fat and waist girth in Japanese obese children
• Criteria for medical intervention in obese children : A new definition of 'Obesity disease' in Japanese children
• Mortality From Congenital Cardiovascular Malformations in Japan, 1968 Through 1997
• Comparison of two assays for fibroblast growth factor (FGF)-23
• COMPARISON OF EFFECTS OF CARDIOPLEGIC SOLUTIONS BY BIOCHEMICAL TECHNIQUES. (EFFECTS OF GLUCOSE AND INSULIN IN CARDIOPLEGIC SOLUTIONS) : Cardiac Surgery I : IInd Auditorium : Proceedings of the 43rd Annual Meeting of the Japanese Circulation Society, Tokyo
• -210-SURGICAL STUDY OF THROMBUS IN MITRAL STENOSIS : Cardiac Surgery : PROCEEDINGS OF THE 42nd ANNUAL MEETING OF THE JAPANESE CIRCULATION SOCIETY
• A VALVE ADVANCEMENT ON VALVULAR INSUFFICIENCY
• A case of 6-pyruvoyl-tetrahydropterin synthase deficiency demonstrates a more significant correlation of L-Dopa dosage with serum prolactin levels than CSF homovanillic acid leyels
• Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency
• Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
• Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population
• Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency
• An Ile/Val polymorphism at codon 1464 of the ATP7A gene
• Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease
• Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism : Comparison between Type 1a and Type 1b
• Transient Central Hypothyroidisim Due to Pituitary Suppression in a Premature Neonate Born to a Mother with Three-Year-Untreated Graves' Disease
• A Girl with Prolactinoma Presenting Cessation of Pubertal Development and Growth
• The Standard Ratio of Upper Segment Length to Lower Segment Length According to Spina Malleolar Distance in Japanese Children
• A 9-Year-Old Girl Presenting Central Precocious Puberty with Polycystic Ovary Syndrome
• Genital Bleeding in a 2-Month-Old Infant with Congenital Adrenal Hyperplasia
• Estrogen Secreting Adrenal Adenocarcinoma in an 18-Month-old Boy: Aromatase Activity, Protein Expression, mRNA and Utilization of Gonadal Type Promoter
• Characterization of Genes Encoding the Pancreatic β-cell ATP-sensitive K^+ Channel in Persistent Hyperinsulinemic Hypoglycemia of Infancy in Japanese Patients
• Molecular and Cellular Regulation of Renal Phosphate Transporters in X-Linked Hypophosphatemia
• SURGICAL CONSIDERATION ON THE COMBINED VALVULAR DISEASES WITH TRICUSPID INSUFFICIENCY : PROCEEDINGS OF THE 38TH ANNUAL MEETING OF THE JAPANESE CIRCULATION SOCIETY
• Clinical Utility of Thyroid Ultrasonography in the Diagnosis of Congenital Hypothyroidism
• Sarcolemmal ATP-sensitive K^+ channels and cardiovascular function
• Guidelines for Diagnosis and Management of Pediatric Food Allergy in Japan
• Therapeutic Guidelines for Atopic Dermatitis 2002
• Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia
• Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
• Self-limited lupus-like presentation of human parvovirus B19 infection in a 1-year-old girl
• Retrocerebellar arachnoid cysts in siblings with mental retardation and undescended testis
• Empty sella syndrome in nevoid basal cell carcinoma syndrome
• γ-Irradiation Deregulates Cell Cycle Control and Apoptosis in Nevoid Basal Cell Carcinoma Syndrome-derived Cells
• A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible : A case report
• Changes in Glycemic Control and Quality of Life in Pediatric Type 1 Diabetics with Continuous Subcutaneous Insulin Infusion of Insulin Aspart Following Multiple Daily Injection Therapy
• Direct demonstration of humorally mediated inhibition of the transcription of phosphate transporter in XLH patients
• Long-Term Outcome of Endocrine Function in Patients with Neurohypophysal Germinomas
• A pediatric patient with acute hepatitis E in Japan
• 1,4-Addition of Diorganozincs to α,β-Unsaturated Ketones Catalyzed by a Copper(I)-Sulfonamide Combined System
• Establishment and Characterization of the Komeda Diabetes-prone Rat as a Segregating Inbred Strain
• Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome
• U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites
• Inhibition of ATP-Sensitive K+ Channels and L-Type Ca2+ Channels by Amiodarone Elicits Contradictory Effect on Insulin Secretion in MIN6 Cells
• Agenesis of the Right Lobe of the Liver:Report of a Case
• DISTRIBUTION OF ATP-SENSITIVE K^+ CHANNELS IN PANCREAS
• Jansen-type Metaphyseal Chondrodysplasia : Analysis of PTH/PTH-related Protein Receptor Messenger RNA by the Reverse Transcriptase-Polymerase Chain Method
• Early Detection of Infants with Hypophosphatemic Vitamin D Resistant Rickets (HDRR)
• A Metastable Precursor in the Oxidation of Si(111)-(7 × 7)
• Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population
• Morphological Changes in Pancreatic Islets of KATP Channel-Deficient Mice : The Involvement of KATP Channels in the Survival of Insulin Cells and the Maintenance of Islet Architecture
• Serotypes of Haemophilus Influenzae Strains Isolated from Pediatric Patients with Respiratory Tract Infections
• A posterior fossa lipoma extending into the cervical spine and subcutaneous space via a cranium bifidum
• Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
• Clinical Characteristics of Obese Japanese Children with Acanthosis Nigricans
• Hydrogen Transfer in Pt-Mo Heterodinuclear Hydride Complexes Promoted by Alkynes
• Enhancement of β-Hydrogen Elimination Reaction on Platinum-containing Heterodinuclear Complexes
• 小児下気道感染症由来インフルエンザ菌の抗菌薬感受性に関する検討
• Value of washed sputum gram stain smear and culture for management of lower respiratory tract infections in children
• A case of persistent Enterobacter cloacae bacteremia
• Impairment of Angiogenic Activity in the Serum From Patients With Coronary Aneurysms Due to Kawasaki Disease
• Incidence of bacterial coinfection with respiratory syncytial virus bronchopulmonary infection in pediatric inpatients
• Changes in leptin and testosterone levels in a girl with congenital adrenal hyperplasia during hydrocortisone therapy
• Increased Production of Vascular Endothelial Growth Factor-D and Lymphangiogenesis in Acute Kawasaki Disease
• Marked pleural and pericardial effusion with elevated Vascular Endothelial Growth Factor production : An uncommon complication of Kawasaki disease
• Efficacy and safety of orally administered pilocarpine hydrochloride for patients with juvenile-onset Sjogren's syndrome
• Genetically modified foods and allergy : assessment of allergenicity (EDUCATIONAL LECTURE) (Proceedings of the 30th Annual Meeting)
• ATP-Sensitive Potassium Channels : Structures, Functions, and Pathophysiology
• Japanese pediatric guidelines for the treatment and management of bronchial asthma 2008
• Hajdu-Cheney syndrome : Infantile onset of hydrocephalus and serpentine fibulae
• 我が国における学童・生徒における肥満と喘息症状との関連
• Sublingual Immunotherapy with House Dust-Extract for House Dust-Mite Allergic Rhinitis in Children
• Establishment of diagnosis by bisulfite-treated methylation-specific PCR method and analysis of clinical characteristics of pseudohypoparathyroidism type 1b
• Inhibition of ATP-Sensitive K^+ Channels and L-Type Ca^ Channels by Amiodarone Elicits Contradictory Effect on Insulin Secretion in MIN6 Cells
• Anti-polyribosylribitol phosphate antibody in pediatric patients with Haemophilus influenzae type b invasive disease
• Three-Year Follow-up of Sirolimus-Eluting Stents vs. Bare Metal Stents for Acute Myocardial Infarction
• Usefulness of Lipoprotein (a) for Predicting Progression of Non-Culprit Coronary Lesions After Acute Myocardial Infarction
• Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
• HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
• A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
• Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
• Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis
• Replication of genetic association studies in asthma and related phenotypes
• Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies
• A Case of Macro Reentrant Atrial Tachycardia around the Coronary Sinus in a Patient with Cardiac Surgery
• Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome
• Japanese Guideline for Atopic Dermatitis
• Isoniazid- and Streptomycin-Resistant Miliary Tuberculosis Complicated by Intracranial Tuberculoma in a Japanese Infant
• A case of infantile Takayasu arteritis with a p.D382E NOD2 mutation : an unusual phenotype of Blau syndrome/early-onset sarcoidosis?

もっと見る 閉じる

スポンサーリンク