Insulin-Like Growth Factors (IGFs) and IGF-Binding Proteins (IGFBP-1, -2 and -3) in Diabetic Pregnancy:Relationship to Macrosomia

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概要

• 論文の詳細を見る
• 1996-04-01

著者

• TSUSHIMA TOSHIO

  Department of Endocrinology, Clinical Institute of Endocrinology, Tokyo Women's Medical University

• YAN-JUN LIU

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• MINEI SATOMI

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• SANAKA MAYUMI

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• NAGASHIMA TAMAKI

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• YANAGISAWA KEIKO

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• OMORI YASUE

  Department of Medicine III(Diabetes Center)Tokyo Women's Medical Colege

• Tsushima T

  Tokyo Women's Medical Univ. Tokyo Jpn

• Tsushima Toshio

  Department Of Endocrinology Clinical Institute Of Endocrinology Tokyo Women's Medical Universit

• Sanaka Mayumi

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Minei S

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Yan-jun Liu

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Nagashima Tamaki

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Yanagisawa Keiko

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Omori Yasue

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Takezaki Toshiro

  Department Of Pediatrics Hokkaido University School Of Medicine

• Minei Satomi

  Department Of Medicine Iii (diabetes Center) Institute Of Clinical Endocrinology Tokyo Women's

• Tajima Toshihiro

  国立成育医療センター 臨床検査部

• TSUSHIMA TOSHIO

  Department of Endocrinology and Endocrine Research Laboratory Toranomon Hospital

関連論文

• Expression of Messenger RNA of Insulin-Like Growth Factors(IGFs)and IGF Binding Proteins(IGFBP1-6)in Placenta of Normal and Diabetic pregnancy
• Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children
• ターナー症候群の新しい参照成長曲線(パーセンタイル曲線)の作成
• Case Study of a 15-Year-old Boy with McCune-Albright Syndrome Combined with Pituitary Gigantism : Effect of Octreotide-long Acting Release (LAR) and Cabergoline Therapy
• Four Japanese Patients with Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism Caused by DAX-1 Gene Mutations : Mutant DAX-1 Failed to Repress Steroidogenic Acute Regulatory Protein (StAR) and Luteinizing Hormone β-subunit Gene Promoter Activi
• A Novel Mutation of the Steroidogenic Acute Regulatory Protein (StAR) Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
• Novel SLC12A1 (NKCC2) Mutations in Two Families with Bartter Syndrome Type 1
• A Novel Missense Mutation (P366T) of the LHX4 Gene Causes Severe Combined Pituitary Hormone Deficiency with Pituitary Hypoplasia, Ectopic Posterior Lobe and a Poorly Developed Sella Turcica
• Two Novel Aquaporin-2 Mutations in a Sporadic Japanese Patient with Autosomal Recessive Nephrogenic Diabetes Insipidus
• A Case of Achondroplasia Associated with Cervicomedullary-Junction Compression
• Two Novel Mutations of Thiazide-Sensitive Na-Cl Cotransporter (TSC) Gene in Two Sporadic Japanese Patients with Gitelman Syndrome
• Turner Syndrome with Crohn Disease
• Two mutations of the Gsα gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia
• Evaluation of Bone Mineral Density in Patients with Turner Syndrome
• A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal
• A Japanese Case with Frasier Syndrome Caused by the Splice Junction Mutation of WT1 Gene
• Mutations of the CYP21 Gene in Nonclassical Steroid 21-Hydroxylase Deficiency in Japan
• Prenatal Diagnosis of Steroid 21-Hydroxylase Deficiency by the Modified Polymerase Chain Reaction to Detect Splice Site Mutation in the CYP21 Gene
• PREDOMINANCE OF THE MUTATION AT 1138 OF THE cDNA FOR THE FIBROBLAST GROWTH FACTOR RECEPTOR 3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA
• A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
• Growth Hormone (GH) Effects on Central Fat Accumulation in Adult Japanese GH Deficient Patients : 6-month Fixed-dose Effects Persist during Second 6-month Individualized-dose Phase
• Metabolic Effects of Human Growth Hormone Isoform (20k-hGH) in Adults with Growth Hormone Deficiency
• Metabolic Effects of Human Growth Hormone Isoform (20 k-hGH) in Adults with Growth Hormone Deficiency
• Serum Concentrations of BNP and ANP in Patients with Thyrotoxicosis
• Leptin Regulation of the Thyroids : Negative Regulation on Thyroid Hormone Levels in Euthyroid Subjects and Inhibitory Effects on Iodide Uptake and Na^+/I^- Symporter mRNA Expression in Rat FRTL-5 Cells
• Increased Expression of Phosphorylated p70S6 Kinase and Akt in Papillary Thyroid Cancer Tissues
• Serum Leptin Levels and Bioelectrical lmpedance Assessment of Body Composition in Patients with Graves' Disease and Hypothyroidism
• Effect of Cytokines on Producton of Insulin-like Growth Factor Binding Proteins (IGFBPs) from Human Fibroblasts in Culture
• Interaction between Leptin and Growth Hormone (GH)/IGF-I Axis
• Expression of Insulin-Like Growth Factor Binding Proteins(IGDBPs)in Human Thyroid Papillary Cancer Tissues
• Expression of Recombinant Human Thyrotropin Receptor in Myeloma Cells
• Pharmacokinetics and Metabolic Effects of High-Dose Growth Hormone Administration in Healthy Adult Men
• Carboxy-Terminal Propeptide of Type 1 Procollagen (P1CP)and Carboxy-Terminal Telopeptide of Type 1 Collagen (1CTP) as Sensitive Markers of Bone Metabolism in Thyroid Disease
• Congenital Malformations in Newborns from Diabetic Mothers
• Seven Cases of Diabetes Mellitus in Turner Syndrome
• Lipohypertrophy in a Patient with Isolated Growth Hormone Deficiency Type IA (IGHD IA) Treated with IGF-I
• Latent Adrenal Insufficiency in Two Patients with Childhood-Onset Pitutary Hormone Deficiency
• INSULIN-LIKE GROWTH FACTOR I AFFECTING CARDIAC HYPERTROPHY IN HUMAN DISEASED MYOCARDIUM : Cardiomyopathy, Myocarditis : 53 Annual Scientific Meeting, Japanese Circulation Society
• Pioglitazone (AD-4833) Ameliorates Insulin Resistance in Patients with NIDDM
• Mortality in Patients with Congenital 21-Hydroxylase Deficiency Diagnosed after the Introduction of a Newborn Screening Program in Japan
• Standardization of Blood Growth Hormone Levels Measured by Different Kits Using a Linear Structural Relationship
• Final Height of Growth Hormone (GH)-Treated Short Children Registered at the Foundation for Growth Science in Japan : Comparison between the Pituitary Human GH Era and the Recombinant Human GH Era
• Postoperative Plasma Cortisol Levels Predict Long-Term Outcome in Patients with Cushing's Disease and Determine Which Patients Should be Treated with Pituitary Irradiation after Surgery
• Registration System for Growth Hormone (GH) Treatment with Standardized Immunoreactive GH Values in Japan
• Growth factors that modulate growth and functions of thyroid cells in culture
• Trends in Age and Anthropometric Data at Start of Growth Hormone Treatment for Girls with Turner Syndrome in Japan
• Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
• Prediction of Pubertal Growth at Start of Estrogen Replacement Therapy in Turner Syndrome
• Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan
• Low-dose Growth Hormone Treatment (0.175mg/kg/week) for Short Stature in Patients with Turner Syndrome : Data from KIGS Japan
• Replacement of Alanine with Asparagic Acid at Position 203 in Human Steroidogenic Acute Regulatory Protein Impairs the Ability to Enhance Steroidogenesis in vitro
• Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency : Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan
• No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment
• Studies of Very Severe Short Stature with Severe GH Deficiency : From the Data Registered with the Foundation for Growth Science
• Serum Levels of 20-Kilodalton Human Growth Hormone (GH) in Children with Simple Obesity
• The Comparison of the Effects of Short-Term Growth Hormone Treatment in Patients with Achondroplasia and with Hypochondroplasia
• Serum Levels of Free Insulin-Like Growth Factor (IGF)-I in Normal Children ; Relations to Total IGF-I, IGF Binding Protein (IGFBP)-1, IGFBP-3, and Acid Labile Subunit (ALS)
• Complications in Adults with Growth Hormone Deficiency : A Survey Study in Japan
• Studies on the Chanracteristics of Hepatic GH Receptor
• Insulin-Like Growth Factors (IGFs) and IGF-Binding Proteins (IGFBP-1, -2 and -3) in Diabetic Pregnancy:Relationship to Macrosomia
• Plasma Membrane Content of Glucose Transporter 4 in Skeletal Muscle and Visceral Fat in OLETF Rats Treated with Troglitazone
• Elevated Serum Bisphenol A Levels under Hyperandrogenic Conditions may be Caused by Decreased UDP-glucuronosyltransferase Activity
• Differences in Serum Bisphenol A Concentrations in Premenopausal Normal Women and Women with Endometrial Hyperplasia
• A Case of Female Pseudohermaphroditism Caused by Aromatase Deficiency
• Viriizing Adrenocortical Carcinoma Invading the Right Atrium with Histological High-Grade Malignancy and p53 Mutation in a 3-Year-Old Child : Indication of Post Operative Adjuvant Chemotherapy
• Disorders of the Hypothalamic-Pituitary-Adrenal Axis Caused by Overdosed Anti-Allergic Drug : A Case Report
• A Ten-Year Old Male with Bromocriptine Resistant PRL and GH-Producing Huge Pituitary Adenoma
• Growth Hormone (GH) Binding Protein in Children with Intrauterine Growth Retardation Treated with High Dose GH
• Japanese Familial Patients with Male-Limited Precocious Puberty
• Genetic and Endocrinological Evaluations of Three 46, XX Patients with Congenital Lipoid Adrenal Hyperplasia Previously Reported as Having Presented Spontaneous Puberty
• Final Height in Girls with Turner Syndrome after Growth Hormone Treatment ; Experience at National Children's Hospital
• Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
• Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
• Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
• A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
• Growth-Promoting and Psychological Effects of High-Dose Growth Hormone Treatment in Children with Intrauterine Growth Retardation
• Spontaneous Growth in Hormone-Treated Short Children
• Growth Response to Growth Hormone Therapy in Patients with Different Degrees of Growth Hormone Deficiency
• Clinical Outcome of GH Treatment in Turner Girls in Japan : Results of Multicentre Trial
• Comparative Concentrations of Growth Hormone-Binding Protein in Maternal Circulation, Fetal Circulation, and Amniotic Fluid
• Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia
• A Simple Method for Purification of Adult Pig Pancreatic Endocrine Cells
• Nutrition Related Hormonal Changes in Obese Children
• Interaction between Endocrine and Immune System
• Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
• A Case of Isolated Growth Hormone Deficiency Associated with Familial Thyroxine Binding Globulin Deficiency
• Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome
• Clinical characteristics of Japanese adults with growth hormone deficiency : a HypoCCS database study
• Long-term Result of Antithyroid Drug Therapy for Graves Disease : Follow up after more than 5 years
• Effect of thyroid hormone on the serum level of somatomedin A.

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