A Germline Mutation, 1001delC, of the Multiple Endocrine Neoplasia Type 1 (MEN 1) Gene in a Japanese Family

スポンサーリンク

概要

著者

関連論文

Preclinical Cushing's Syndrome Due to ACTH-independent Bilateral Macronodular Adrenocortical Hyperplasia with Excessive Secretion of 18-hydroxydeoxycorticosterone and Corticosterone
A Germline Mutation, 1001delC, of the Multiple Endocrine Neoplasia Type 1 (MEN 1) Gene in a Japanese Family
Induction of Autoimmune Hypothyroidism and Subsequent Hyperthyroidism by TSH Receptor Antibodies following Subacute Thyroiditis: A Case Report
Blood Pressure Control in Japanese Hypertensives with or without Type 2 Diabetes Mellitus
A Patient of Hypogonadotropic Hypogonadism Accompanied by Growth Hormone Deficiency and Decreased Bone Mineral Density Who Attained Normal Growth
A Case of Renin-Producing Adrenocortical Cancer
Hypercalcemia Accompanied by Hypothalamic Hypopituitarism, Central Diabetes Inspidus and Hyperthyroidism
Glucose Intolerance in Spontaneously Hypertensive and Wistar-Kyoto Rats: Enhanced Gene Expression and Synthesis of Skeletal Muscle Glucose Transporter 4
Decrease in Serum Levels of Thyroid Hormone in Patients with Coronary Heart Disease
Modulation of Reactive Oxygen Species in Endothelial Cells by Peroxynitrite-Treated Lipoproteins
Novel S100 Proteins in Human Esophageal Epithelial Cells : CAAF 1 Expression is Associated with Cell Growth Arrest
Protective Effect of Recombinant Human Leukemia Inhibitory Factor against Thrombocytopenia in Carboplatin-treated Mice
In vivo Effect of Recombinant Human Leukemia Inhibitory Factor in Primates
Cytokine Production in Five Tumor Cell Lines with Activity to Induce Cancer Cachexia Syndrome in Nude Mice
Components of Metabolic Syndrome and their Combinations as Predictors of Cardiovascular Disease in Japanese Patients with Type 2 Diabetes. Implications for Improved Definition. Analysis from Japan Diabetes Complications Study (JDCS)
Metformin Decrease Blood Pressure and Obesity in OLETF rats Via Improvement of Insulin Resistance
Effect of p53 Deficiency on External Vascular Cuff-Induced Neointima Formation
Effects of disruption of p53 gene on vascular neointima formation
Enzyme-linked Immunosorbent Assay of Pro-gastrin-releasing Peptide for Small Cell Lung Cancer Patients in Comparison with Neuron-specfic Enolase Measurement
The NGFI-B Family: Orphan Nuclear Receptors of the Steroid/Thyroid Receptor Superfamily
A Novel Somatic Point Mutation of the RET Proto-oncogene in Tumor Tissues of Small Cell Lung Cancer Patients
Germline Mutations of the MEN1 Gene in Japanese Kindred with Multiple Endocrine Neoplasia Type 1
Primary Hyperparathyroidism Associatiated with Aldosterone-Producing Adrenocortical Adenoma and Breast Cancer : Relation to MEN1 Gene
Measuring Serum Thyroglobulin in Patients with Follicular Thyroid Nodule : Its Diagnostic Implications
A Large Germline Deletion of the MEN1 Gene in a Family with Multiple Endocrine Neoplasia Type 1
Two Germline Missense Mutations at Codons 804 and 806 of the RET Protooncogene in the Same Allele in a Patient with Multiple Endocrine Neoplasia Type 2B without Codon 918 Mutation
A Novel Somatic Mutation in the RET Proto-oncogene in Familial Medullary Thyroid Carcinoma with a Germline Codon 768 Mutation
Bilateral Adrenalectomy with Autotransplantation of Adrenocortical Tissue or Unilateral Adrenalectomy:Treatment Options for Pheochromocytomas in Multiple Endocrine Neoplasia Type 2A
Preclinical Cushing's Syndrome Due to ACTH-independent Bilateral Macronodular Adrenocortical Hyperplasia with Excessive Secretion of 18-hydroxydeoxycorticosterone and Corticosterone
The NGFI-B Family : Orphan Nuclear Receptors of the Steroid/Thyroid Receptor Superfamily
Disturbed Lipid Metabolism in Patients with Subclinical Hypothyroidism: Effect of L-Thyroxine Therapy.
A Novel Point Mutation of the RET Proto-oncogene in Small Cell Lung Carcinoma Cell Lines.
Incidence of Anti-Mouse IgG in normal subjects and Patients with Autoimmune Thyroid Disease.

もっと見る

スポンサーリンク