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Human Genetics|April 1, 1989
Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.
Cancer Research|May 19, 2001
Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomasP Heimann, H El Housni, G Ogur, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messengerH M Targovnik, G Medeiros-Neto, V Varela, et al.
Cellular and Molecular Life Sciences : CMLS|April 29, 2008
The specificity of binding of glycoprotein hormones to their receptorsG Caltabiano, M Campillo, A De Leener, et al.
Endocrinology|January 1, 1997
Costimulation of adenylyl cyclase and phospholipase C by a mutant alpha 1B-adrenergic receptor transgene promotes malignant transformation of thyroid follicular cellsC Ledent, J F Denef, S Cottecchia, et al.
Molecular and Cellular Endocrinology|October 1, 1990
Use of the recombinant human thyrotropin receptor (TSH-R) expressed in mammalian cell lines to assay TSH-R autoantibodiesM Ludgate, J Perret, M Parmentier, et al.
The EMBO Journal|February 16, 2002
Tyrosine sulfation is required for agonist recognition by glycoprotein hormone receptorsS Costagliola, V Panneels, M Bonomi, et al.
The Journal of Clinical Investigation|December 1, 1991
A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidismT Ieiri, P Cochaux, H M Targovnik, et al.
FEBS Letters|April 6, 1992
Functional role of TTF-1 binding sites in bovine thyroglobulin promoterF Javaux, F Bertaux, A Donda, et al.
Molecular and Cellular Endocrinology|April 1, 1994
Constitutively active receptors as a disease-causing mechanismJ Parma, L Duprez, J Van Sande, et al.
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