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Endocrine Reviews|April 1, 1993
Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidismG Medeiros-Neto, H M Targovnik, G VassartThe 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.Thyroid : Official Journal of the American Thyroid Association|May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidismH M Targovnik, G D Frechtel, F M Mendive, et al.Molecular and Cellular Endocrinology|March 1, 1992
Identification of a minor Tg mRNA transcript in RNA from normal and goitrous thyroidsH M Targovnik, P Cochaux, D Corach, et al.Thyroid : Official Journal of the American Thyroid Association|January 1, 1991
Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesisH M Targovnik, V Varela, C Abatangelo, et al.Thyroid : Official Journal of the American Thyroid Association|October 19, 1999
Genomic organization of the 3' region of the human thyroglobulin geneF M Mendive, C M Rivolta, G Vassart, et al.Thyroid : Official Journal of the American Thyroid Association|August 1, 1997
Identification of a new thyroglobulin variant: a guanine-to-adenine transition resulting in the substitution of arginine 2510 by glutamineF M Mendive, L C Rossetti, G Vassart, et al.European Journal of Biochemistry|June 1, 1984
Structural organization of the 5' region of the human thyroglobulin geneH M Targovnik, V Pohl, D Christophe, et al.Thyroid : Official Journal of the American Thyroid Association|August 4, 2001
Congenital goiter with hypothyroidism caused by a 5' splice site mutation in the thyroglobulin geneH M Targovnik, C M Rivolta, F M Mendive, et al.European Journal of Endocrinology|October 3, 2001
Genomic organization of the human thyroglobulin gene: the complete intron-exon structureF M Mendive, C M Rivolta, C M Moya, et al.Pageof 34