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Kim, P S; Hossain, S A; Park, Y N et al. (1998) 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. Proc Natl Acad Sci U S A 95:9909-13
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Kim, P S; Arvan, P (1998) Endocrinopathies in the family of endoplasmic reticulum (ER) storage diseases: disorders of protein trafficking and the role of ER molecular chaperones. Endocr Rev 19:173-202
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Arvan, P; Kim, P S; Kuliawat, R et al. (1997) Intracellular protein transport to the thyrocyte plasma membrane: potential implications for thyroid physiology. Thyroid 7:89-105
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Medeiros-Neto, G; Kim, P S; Yoo, S E et al. (1996) Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones. J Clin Invest 98:2838-44
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Prabakaran, D; Kim, P S; Dixit, V M et al. (1996) Oligomeric assembly of thrombospondin in the endoplasmic reticulum of thyroid epithelial cells. Eur J Cell Biol 70:134-41
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Kim, P S; Kwon, O Y; Arvan, P (1996) An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism. J Cell Biol 133:517-27
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Kim, P S; Arvan, P (1995) Calnexin and BiP act as sequential molecular chaperones during thyroglobulin folding in the endoplasmic reticulum. J Cell Biol 128:29-38
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Kim, P S; Arvan, P (1993) Hormonal regulation of thyroglobulin export from the endoplasmic reticulum of cultured thyrocytes. J Biol Chem 268:4873-9
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Kim, P S; Kim, K R; Arvan, P (1993) Disulfide-linked aggregation of thyroglobulin normally occurs during nascent protein folding. Am J Physiol 265:C704-11
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