Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport
スポンサーリンク
概要
著者
-
MASAWA Nobuhide
Department of Anatomic and Diagnostic Pathology, Dokkyo University School of Medicine
-
HISHINUMA Akira
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine
-
IEIRI Tamio
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine
-
Masawa Nobuhide
Department Of Anatomic And Diagnostic Pathology Dokkyo University School Of Medicine
-
Masawa Nobuhide
Department Of Pathology
-
KASAI Kikuo
Department of Endocrinology
-
KANNO Yumiko
Sumitomo Metal Bio-Science Inc.
-
ARIMURA Miwako
Department of Clinical Pathology
-
SHIMODA Shin-ichi
Department of Endocrinology
-
Ieiri Tamio
Department Of Clinical Laboratory Medicine Dokkyo University School Of Medicine
-
Hishinuma Akira
獨協医科大学
-
Hishinuma Akira
Department Of Clinical Laboratory Medicine Dokkyo Medical University
関連論文
- Castleman's Disease of the Retroperitoneum : With Special Reference to IgG4-Related Disorder
- Cyclin D1 Protein Overexpression in Extramedullary Plasmacytoma : A Clinicopathologic Study of 11 Cases
- "Follicular Variant" of Hyaline-vascular Type of Castleman's Disease : Histopathological and Immunohistochemical Study of 11 Cases
- B-Cell Lymphoma Associated with Sjogren's Syndrome among Japanese Patients : A Clinicopathologic and Immunohistochemical Study of 15 Cases
- Atypical Lymphoplasmacytic and Immunoblastic Proliferation of Autoimmune Disease : Clinicopathologic and Immunohistochemical Study of 9 Cases
- Usefulness of immunohistochemistry for recognizing metastatic colorectal adenocarcinoma in infarcted lymph nodes
- Hepatic angiomyolipoma resembling an inflammatory pseudotumor of the liver : A case report
- Lymph node lesion in infectious mononucleosis showing geographic necrosis containing cytologically atypically B-cells. A case report
- A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels
- Case of Werner's syndrome with pancreatic carcinoma
- The Role of Oxidative Stress on Pathogenesis of Hypertensive Arterial Lesions in Rat Mesenteric Arteries
- Reactive follicular hyperplasia in the lymph node lesions from systemic lupus erythematosus patients: A clinicopathological and immunohistological study of 21 cases
- Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese Patient
- Pathologic Evidence of Microvascular Rarefaction in the Brain of Renal Hypertensive Rats
- The pathogenesis of cerebrovascular lesions in hypertensive rats
- Pathology of a dissecting intracranial aneurysm
- JTII-28 CYTOLOGIC FEATURES OF NEUROENDOCRINE TUMORS OF THE LUNG-ESPECIALLY IN LARGE CELL NEUROENDOCRINE CARCINOMA
- Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport
- Expression of Thyroid Hormone Receptor Isoforms Down-regulated by Thyroid Hormone in Human Medulloblastoma Cells
- A Novel Splice Variant of the Nuclear Coactivator p120 Functions Strongly for Androgen Receptor : Characteristic Expression in Prostate Disease
- Sequence Analysis of Thyroid Transcription Factor-2 (TTF-2) Gene in Ten Patients with Congenital Hypothyroidism due to Thyroid Dysgenesis
- Sequence Analysis of Thyroid Transcription Factor-1 Gene Reveals Absence of Mutations in Patients with Thyroid Dysgenesis but Presence of Polymorphisms in the 5' Flanking Region and Intron
- A Novel Thyrotropin Receptor Germline Mutation (Asp617Tyr) Causing Hereditary Hyperthyroidism
- Herbal Medicine, Hachimi-jio-gan, and Its Component Cinnamomi Cortex Activate the Peroxisome Proliferator-activated Receptor Alpha in Renal Cells
- Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene
- Atypical Lymphoplasmacytic and Immunoblastic Proliferation of Autoimmune Disease : Clinicopathologic and Immunohistochemical Study of 9 Cases
- Effect of Poly (ADP-ribose) Polymerase Inhibitors on Hypoadiponectinemia Caused by Chronic Blockade of Nitric Oxide Synthesis in Rats
- Genetic thyroid diseases in Japan featured by thyroglobulin mutations
- Telmisartan inhibits cytokine-induced nuclear factor-κB activation independently of the peroxisome proliferator-activated receptor-γ
- Emergence of NDM-1-positive capsulated Escherichia coli with high resistance to serum killing in Japan
- Comparative study between high-dose fluvastatin and low-dose fluvastatin and ezetimibe with regard to the effect on endothelial function in diabetic patients
- Ventricular Fibrillation Due to Severe Hypokalemia Induced by Steroid Treatment in a Patient with Thyrotoxic Periodic Paralysis
- Lymph Node Lesion of Acute Infectious Mononucleosis in the Elderly : A Case Report
- A Case of Myeloma with Hypercalcemia Caused by High Serum Concentrations of both Parathyroid Hormone-related Peptide (PTHrP) and Macrophage Inflammatory Protein-1.ALPHA. (MIP-1.ALPHA.)
- A case of pituitary apoplexy with spontaneous recovery.
- Clinical Study on Early Changes in Thyroid Function of Hyperthyroidism Treated with Propylthiouracil and a Relatively Small Dose of Iodide
- Epithelioid Cell Granulomatous Response of Waldeyer's Ring among Japanese : A Clinicopathological and Immunohistochemical Study of 16 Cases
- Presence of Immunoglobulin Heavy Chain Rearrangement in So-Called IgG4-Related Plasma Cell Granuloma of the Eyelid
- Improvement in abnormal secretion of thyrotropin and gonadotropin after restoration of serum calcium in pseudohypoparathyroidism.
- Characterisation of Apoptosis in myb-Transformed Hematopoietic Cell (MTHC-A) Lines : TNF-α-Induced Apoptosis and Prevention by cAMP#
- An ACTH-secreting Pituitary Adenoma Within the Sphenoid Sinus
- Epithelioid Cell Granulomatous Response of Waldeyer's Ring among Japanese : A Clinicopathological and Immunohistochemical Study of 16 Cases