A Natural Transactivation Mutation in the Thyroid Hormone β receptor: Impaired Interaction with Putative Transcriptional Mediators von Collingwood, T. N., Rajanayagam, O., Adams, M., Wagner, R., Cavaillès, V., Kalkhoven, E., Mathews, C., Nystrom, E., Stenlof, K., Lindstedt, G., Tisell, L., Fletterick, R. J., Parker, M. G., Chatterjee, V. K. K.

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Prenatal Diagnosis of Thyroid Hormone Resistance von Asteria, C, Rajanayagam, O, Collingwood, T. N, Persani, L, Romoli, R, Mannavola, D, Zamperini, P, Buzi, F, Ciralli, F, Chatterjee, V. K. K, Beck-Peccoz, P

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Retardation of post-natal development caused by a negatively acting thyroid hormone receptor α1 von Tinnikov, Alexander, Nordström, Kristina, Thorén, Peter, Kindblom, Jenny M., Malin, Stephen, Rozell, Björn, Adams, Maria, Rajanayagam, Odelia, Pettersson, Sven, Ohlsson, Claes, Chatterjee, Krishna, Vennström, Björn

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A Dominant-negative Peroxisome Proliferator-activated Receptor γ (PPARγ) Mutant Is a Constitutive Repressor and Inhibits PPARγ-mediated Adipogenesis von Gurnell, Mark, Wentworth, John M., Agostini, Maura, Adams, Maria, Collingwood, Trevor N., Provenzano, Claudia, Browne, Paul O., Rajanayagam, Odelia, Burris, Thomas P., Schwabe, John W., Lazar, Mitchell A., Chatterjee, V.Krishna K.

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Neonatal thyrotoxicosis and maternal infertility in thyroid hormone resistance due to a mutation in the TRβ gene (M313T) von Blair, J. C., Mohan, U., Larcher, V. F., Rajanayagam, O., Burrin, J. M., Perry, L. A., Grossman, A. B., Chatterjee, V. K. K., Savage, M. O.

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Reversible Pituitary Enlargement in the Syndrome of Resistance to Thyroid Hormone von Gurnell, M, Rajanayagam, O, Barbar, I, Jones, M K, Chatterjee, V K

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Digenic inheritance of severe insulin resistance in a human pedigree von O'Rahilly, Stephen, Savage, David B, Agostini, Maura, Barroso, Inês, Gurnell, Mark, Luan, Jian'an, Meirhaeghe, Aline, Harding, Anne-Helen, Ihrke, Gudrun, Rajanayagam, Odelia, Soos, Maria A, George, Stella, Berger, Dirk, Thomas, E. Louise, Bell, Jimmy D, Meeran, Karim, Ross, Richard J, Vidal-Puig, Antonio, Wareham, Nicholas J, Chatterjee, V. Krishna K, Schafer, Alan J

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Three novel mutations at serine 314 in the thyroid hormone beta receptor differentially impair ligand binding in the syndrome of resistance to thyroid hormone von Gurnell, M, Rajanayagam, O, Agostini, M, Clifton-Bligh, R J, Wang, T, Zelissen, P M, van der Horst, F, van de Wiel, A, Macchia, E, Pinchera, A, Schwabe, J W, Chatterjee, V K

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Tyrosine Agonists Reverse the Molecular Defects Associated with Dominant-Negative Mutations in Human Peroxisome Proliferator-Activated Receptor γ von Agostini, Maura, Gurnell, Mark, Savage, David B, Wood, Emily M, Smith, Aaron G, Rajanayagam, Odelia, Garnes, Keith T, Levinson, Sidney H, Xu, H. Eric, Schwabe, John W. R, Willson, Timothy M, O’Rahilly, Stephen, Chatterjee, V. Krishna

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Three Novel Mutations at Serine 314 in the Thyroid Hormone β Receptor Differentially Impair Ligand Binding in the Syndrome of Resistance to Thyroid Hormone1 von Gurnell, M, Rajanayagam, O, Agostini, M, Clifton-Bligh, R. J. D, Wang, T, Zelissen, P. M. J, van der Horst, F, Wiel, A. van de, Macchia, E, Pinchera, A, Schwabe, J. W. R, Chatterjee, V. K. K

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A role for helix 3 of the TRβ ligand-binding domain in coactivator recruitment identified by characterization of a third cluster of mutations in resistance to thyroid hormone von Collingwood, Trevor N., Wagner, Richard, Matthews, Clare H., Clifton-Bligh, Rory J., Gurnell, Mark, Rajanayagam, Odelia, Agostini, Maura, Fletterick, Robert J., Beck-Peccoz, Paolo, Reinhardt, Walter, Binder, Gerhard, Ranke, Michael B., Hermus, Ad, Hesch, Rolf D., Lazarus, John, Newrick, Paul, Parfitt, Vernon, Raggatt, Peter, de Zegher, Francis, Chatterjee, V.Krishna K.

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Neonatal thyrotoxicosis and maternal infertility in thlyroid hormone resistance due to a mutation in the TR(beta) gene (M313T) von Blair, J C, Mohan, U, Larcher, V F, Rajanayagam, O

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Prenatal diagnosis of thyroid hormone resistance von ASTERIA, C, RAJANAYAGAM, O, BECK-PECCOZ, P, COLLINGWOOD, T. N, PERSANI, L, ROMOLI, R, MANNAVOLA, D, ZAMPERINI, P, BUZI, F, CIRALLI, F, CHATTERJEE, V. K. K

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Retardation of post-natal development caused by a negatively acting thyroid hormone receptor [alpha]1 von Tinnikov, Alexander, Nordstrom, Kristina, Thoren, Peter, Kindblom, Jenny M, Malin, Stephen, Rozell, Bjorn, Adams, Maria, Rajanayagam, Odelia, Pettersson, Sven, Ohlsson, Claes, Chatterjee, Krishna, Vennstrom, Bjorn

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Retardation of post-natal development caused by a negatively acting thyroid hormone receptor alpha1 von Tinnikov, Alexander, Nordström, Kristina, Thorén, Peter, Kindblom, Jenny M, Malin, Stephen, Rozell, Björn, Adams, Maria, Rajanayagam, Odelia, Pettersson, Sven, Ohlsson, Claes, Chatterjee, Krishna, Vennström, Björn

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Neonatal thyrotoxicosis and maternal infertility in thyroid hormone resistance due to a mutation in the TRbeta gene (M313T) von Blair, J C, Mohan, U, Larcher, V F, Rajanayagam, O, Burrin, J M, Perry, L A, Grossman, A B, Chatterjee, V K K, Savage, M O

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Contrasting Phenotypes in Resistance to Thyroid Hormone Alpha Correlate with Divergent Properties of Thyroid Hormone Receptor α1 Mutant Proteins von Moran, C, Agostini, M, McGowan, A, Schoenmakers, E, Fairall, L, Lyons, G, Rajanayagam, O, Watson, L, Offiah, O, Barton, J, Price, S, Schwabe, J, Chatterjee, VKK

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Contrasting phenotypes in resistance to thyroid hormone alpha correlate with divergent properties of thyroid hormone receptor α1 mutant proteins von Moran, C, Agostini, M, McGowan, A, Schoenmakers, E, Fairall, L, Lyons, G, Rajanayagam, O, Watson, L, Offiah, A, Barton, J, Price, S, Schwabe, J, Chatterjee, K

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Erratum: Digenic inheritance of severe insulin resistance in a human pedigree von Savage, D B, Agostini, M, Barroso, I, Gurnell, M, Luan, J, Meirhaeghe, A, Harding, A-H, Ihrke, G, Rajanayagam, O, Soos, M A, George, S, Berger, D, Thomas, E L, Bell, J D, Meeran, K, Ross, R J, Vidal-Puig, A, Wareham, N J, O'Rahilly, S, Chatterjee, V K K, Schafer, A J

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Supplementary Material for: Clinical Consequences of Variable Results in the Measurement of Free Thyroid Hormones: Unusual Presentation of a Family with a Novel Variant in the THRB... von I., Campi, M., Agostini, F., Marelli, T., deFilippis, B., Romartinez-Alonso, O., Rajanayagam, G., Rurale, I., Gentile, F., Spagnolo, M., Andreasi, F., Ferraù, S., Cannavò, L., Fugazzola, K.V., Chatterjee, L., Persani

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