スポンサーリンク
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine | 論文
- A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels
- Protoctive Effects of a Novel Drug, K201 (JTV519), on Reperfusion Injury in Experimental Acute Myocardial Infarction (Cardiovascular Pharmacology, Basic/Clinical 3 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese Patient
- Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport
- 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
- Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene