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Thyroglobulin From Molecular and Cellular Biology to Clinical EndocrinologyDi Jeso, Bruno ; Arvan, PeterEndocrine reviews, 2016-02, Vol.37 (1), p.2-36 [Periódico revisado por pares]United States: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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A frequent oligogenic involvement in congenital hypothyroidismde Filippis, Tiziana ; Gelmini, Giulia ; Paraboschi, Elvezia ; Vigone, Maria Cristina ; Di Frenna, Marianna ; Marelli, Federica ; Bonomi, Marco ; Cassio, Alessandra ; Larizza, Daniela ; Moro, Mirella ; Radetti, Giorgio ; Salerno, Mariacarolina ; Ardissino, Diego ; Weber, Giovanna ; Gentilini, Davide ; Guizzardi, Fabiana ; Duga, Stefano ; Persani, LucaHuman molecular genetics, 2017-07, Vol.26 (13), p.2507-2514 [Periódico revisado por pares]EnglandTexto completo disponível |
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Material Type: Artigo
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Defects in protein folding in congenital hypothyroidismTargovnik, Héctor M. ; Scheps, Karen G. ; Rivolta, Carina M.Molecular and cellular endocrinology, 2020-02, Vol.501, p.110638-110638, Article 110638 [Periódico revisado por pares]Ireland: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Allosteric Activation Dictates PRC2 Activity Independent of Its Recruitment to ChromatinLee, Chul-Hwan ; Yu, Jia-Ray ; Kumar, Sunil ; Jin, Ying ; LeRoy, Gary ; Bhanu, Natarajan ; Kaneko, Syuzo ; Garcia, Benjamin A. ; Hamilton, Andrew D. ; Reinberg, DannyMolecular cell, 2018-05, Vol.70 (3), p.422-434.e6 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Hypothyroid myopathy: A peculiar clinical presentation of thyroid failure. Review of the literatureSindoni, Alessandro ; Rodolico, Carmelo ; Pappalardo, Maria Angela ; Portaro, Simona ; Benvenga, SalvatoreReviews in Endocrine & Metabolic Disorders, 2016-12, Vol.17 (4), p.499-519 [Periódico revisado por pares]New York: Springer USTexto completo disponível |
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Material Type: Artigo
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Congenital hypothyroidism and thyroid cancerPenna, Gustavo ; Rubio, Ileana G S ; Brust, Ester Saraiva ; Cazarin, Juliana ; Hecht, Fabio ; Alkmim, Nina Ramalho ; Rajão, Kamilla M A Brandão ; Ramos, Helton EstrelaEndocrine-related cancer, 2021-09, Vol.28 (9), p.R217-R230 [Periódico revisado por pares]England: Bioscientifica LtdTexto completo disponível |
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Material Type: Artigo
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Iodide Handling Disorders (NIS, TPO, TG, IYD)Targovnik, Héctor M., PhD ; Citterio, Cintia E., PhD ; Rivolta, Carina M., PhDBest Practice & Research Clinical Endocrinology & Metabolism, 2017-03, Vol.31 (2), p.195-212 [Periódico revisado por pares]Netherlands: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Genetic causes of congenital hypothyroidism due to dyshormonogenesisGrasberger, Helmut ; Refetoff, SamuelCurrent opinion in pediatrics, 2011-08, Vol.23 (4), p.421-428 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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The role of iodine in human growth and developmentZimmermann, Michael B.Seminars in cell & developmental biology, 2011-08, Vol.22 (6), p.645-652 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Thyroglobulin Interactome Profiling Defines Altered Proteostasis Topology Associated With Thyroid DyshormonogenesisWright, Madison T. ; Kouba, Logan ; Plate, LarsMolecular & cellular proteomics, 2021-01, Vol.20, p.100008-100008, Article 100008 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |