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The Journal of Clinical Endocrinology and Metabolism|August 18, 2000
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxineS Pannain, M Feldman, U Eiholzer, et al.
Acta Endocrinologica|February 1, 1982
Radioimmunoassay detection of endorphins from long-term culture of human pituitary tumour cellsB Sharp, S Melmed, R Goldberg, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1994
A new point mutation (C446R) in the thyroid hormone receptor-beta gene of a family with resistance to thyroid hormoneR E Weiss, B Chyna, P B Duell, et al.
Metabolism: Clinical and Experimental|January 1, 1975
Differentiation of two abnormalities in thyroid peroxidase causing organification defect and goitrous hypothyroidismH Niepomniszcze, A L Rosenbloom, L J Degroot, et al.
The Journal of Clinical Investigation|April 16, 1998
Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice siteJ Pohlenz, I M Rosenthal, R E Weiss, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1995
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type IP E Macchia, H H Harrison, N H Scherberg, et al.
Molecular Endocrinology (Baltimore, Md.)|March 1, 1992
An additional carbohydrate chain in the variant thyroxine-binding globulin-Gary (TBGAsn-96) impairs its secretionF Kambe, H Seo, Y Mori, et al.
Biochemical and Biophysical Research Communications|December 6, 1997
Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter geneJ Pohlenz, G Medeiros-Neto, J L Gross, et al.
Journal of Endocrinological Investigation|July 6, 2004
A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1)D Mannavola, L C Moeller, P Beck-Peccoz, et al.
Molecular and Cellular Endocrinology|November 12, 1990
Thyrotropin activates both the cyclic AMP and the PIP2 cascades in CHO cells expressing the human cDNA of TSH receptorJ Van Sande, E Raspé, J Perret, et al.
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