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S Refetoff

Showing results (191-200 of 271) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 1, 1981
Effects of "jet lag" on hormonal patterns. II. Adaptation of melatonin circadian periodicityM Fève-Montange, E Van Cauter, S Refetoff, et al.
Thyroid : Official Journal of the American Thyroid Association|January 26, 2000
Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormoneJ Pohlenz, A Maqueem, K Cua, et al.
Clinical Endocrinology|January 1, 1977
Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidaseH Niepomniszcze, G A Medeiros-Neto, S Refetoff, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
The relative expression of mutant and normal thyroid hormone receptor genes in patients with generalized resistance to thyroid hormone determined by estimation of their specific messenger ribonucleic acid productsY Hayashi, O E Janssen, R E Weiss, et al.
Thyroid : Official Journal of the American Thyroid Association|January 1, 1994
Resistance to thyroid hormone in subjects from two unrelated families is associated with a point mutation in the thyroid hormone receptor beta gene resulting in the replacement of the normal proline 453 with serineS Refetoff, R E Weiss, J R Wing, et al.
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.
The Journal of Clinical Investigation|March 23, 2000
Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' diseaseS Costagliola, M C Many, J F Denef, 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.
Pageof 28

Showing results (191-200 of 271) with videos related to

Sort By:
Pageof 28
The Journal of Clinical Endocrinology and Metabolism|April 1, 1981
Effects of "jet lag" on hormonal patterns. II. Adaptation of melatonin circadian periodicityM Fève-Montange, E Van Cauter, S Refetoff, et al.
Thyroid : Official Journal of the American Thyroid Association|January 26, 2000
Improved radioimmunoassay for measurement of mouse thyrotropin in serum: strain differences in thyrotropin concentration and thyrotroph sensitivity to thyroid hormoneJ Pohlenz, A Maqueem, K Cua, et al.
Clinical Endocrinology|January 1, 1977
Familial goitre with partial iodine organification defect, lack of thyroglobulin, and high levels of thyroid peroxidaseH Niepomniszcze, G A Medeiros-Neto, S Refetoff, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1993
The relative expression of mutant and normal thyroid hormone receptor genes in patients with generalized resistance to thyroid hormone determined by estimation of their specific messenger ribonucleic acid productsY Hayashi, O E Janssen, R E Weiss, et al.
Thyroid : Official Journal of the American Thyroid Association|January 1, 1994
Resistance to thyroid hormone in subjects from two unrelated families is associated with a point mutation in the thyroid hormone receptor beta gene resulting in the replacement of the normal proline 453 with serineS Refetoff, R E Weiss, J R Wing, et al.
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.
The Journal of Clinical Investigation|March 23, 2000
Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' diseaseS Costagliola, M C Many, J F Denef, 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.
Pageof 28