Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene von KOPP, P, ARSEVEN, O. K, SABACAN, L, KOTLAR, T, DUPUIS, J, CAVALIERE, H, SANTOS, C. L. S, JAMESON, J. L, MEDEIROS-NETO, G

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Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil von Nogueira, C R, Kopp, P, Arseven, O K, Santos, C L, Jameson, J L, Medeiros-Neto, G

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Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid Hypoplasia von Nogueira, C R, Nguyen, L Q, Coelho-Neto, J R, Arseven, O K, Jameson, J L, Kopp, P, Medeiros-Neto, G A

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Proteolysis of the Mismatch Repair Protein MLH1 by Caspase-3 Promotes DNA Damage-induced Apoptosis von Chen, Feng, Arseven, Onur K., Cryns, Vincent L.

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Clinical and molecular analysis of three Mexican families with Pendred's syndrome von GONZALEZ TREVINO, O, KARAMANOGLU ARSEVEN, O, CEBALLOS, C. J, VIVES, V. I, RAMIREZ, R. C, GOMEZ, V. V, MEDEIROS-NETO, G, KOPP, P

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Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism von Nguyen, Lynda Q, Arseven, Onur Karamanoglu, Gerber, Hans, Stein, Barbara S, Jameson, J Larry, Kopp, Peter

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Substitutions of Tyrosine 601 in the Human Thyrotropin Receptor Result in Increase or Loss of Basal Activation of the Cyclic Adenosine Monophosphate Pathway and Disrupt Coupling to... von Arseven, O K, Wilkes, W P, Jameson, J L, Kopp, P

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The thyroid hormone receptor variant alpha2 is a weak antagonist because it is deficient in interactions with nuclear receptor corepressors von Tagami, T, Kopp, P, Johnson, W, Arseven, O K, Jameson, J L

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