Low-Molecular-Weight Iodoproteins in the Congenital Goiters of cog/cog Mice*
Author:
Publisher
Mary Ann Liebert Inc
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.liebertpub.com/doi/pdf/10.1089/thy.1992.2.329
Reference22 articles.
1. Primary structure of human thyroglobulin deduced from the sequence of its 8448-base complementary DNA
2. HEREDITARY CONGENITAL GOITRE WITH THYROGLOBULIN DEFICIENCY CAUSING HYPOTHYROIDISM
3. Low Molecular Weight Thyroglobulin Leading to a Goiter in a 12-Year-Old Girl*
4. Normal Level of Thyroglobulin Messenger Ribonucleic Acid ina Human Congenital Goiter with Thyroglobulin Deficiency*
5. Hereditary Congenital Goiter with Thyroglobulin Deficiency in a Breed of Goats*
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4. The Acetylcholinesterase Homology Region Is Essential for Normal Conformational Maturation and Secretion of Thyroglobulin;Journal of Biological Chemistry;2004-04
5. A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: A model of human endoplasmic reticulum storage diseases;Proceedings of the National Academy of Sciences;1998-08-18
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