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Biochemical and Biophysical Research Communications|February 14, 1990
Expression of human pregnancy specific beta 1 glycoprotein (PSG) genes during placental developmentC Streydio, G VassartThe Journal of Clinical Investigation|October 1, 1992
Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiterM J Abramowicz, H M Targovnik, V Varela, et al.The Journal of Clinical Endocrinology and Metabolism|February 1, 1985
X-chromosome-linked inheritance of the variant thyroxine-binding globulin in Australian aboriginesS Refetoff, Y MurataBiochimie|July 14, 1999
Mutations in the sodium/iodide symporter (NIS) gene as a cause for iodide transport defects and congenital hypothyroidismJ Pohlenz, S RefetoffBiochimica Et Biophysica Acta|March 18, 1977
Iodination-deiodination. A radiochemical method for detection of structure and changes in structure in RNAN Scherberg, S RefetoffThe Journal of Clinical Endocrinology and Metabolism|November 1, 1986
Inherited heat-stable variant thyroxine-binding globulin (TBG-Chicago)J Takamatsu, S RefetoffThe Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSHJ Xie, S Pannain, J Pohlenz, et al.Thyroid : Official Journal of the American Thyroid Association|October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptorD Tiosano, S Pannain, G Vassart, et al.Bailliere'S Clinical Endocrinology and Metabolism|January 1, 1995
The thyrotropin receptor as a model to illustrate receptor and receptor antibody diseasesM E Ludgate, G VassartPageof 46