Several lines of research have been developed by using mice as animal models, including goiter development and involution, nodules formation and congenital hypothyroidism. They are reviewed and discussed as potential tools to better understand the thyroid pathophysiology
Graves' disease is characterized by overstimulation of the thyroid gland with agonistic autoantibodi...
Graves’ disease is the most common form of autoimmune thyroid disorder, characterized by hyperthyroi...
Background: Mutations in the SLC26A4 gene, coding for the anion transporter pendrin, are responsible...
Gene targeting technology has allowed the generation of mouse mutants which lack specific genes. The...
We have investigated thyroid structure and function in mice homozygous for the chromosome 15 mutatio...
Unless treated, congenital hypothyroidism causes severe mental retardation, stunted physical develop...
The NOD mouse, an ideal model for insulin-dependent diabetes mellitus, is also useful to study the p...
Congenital goiter (cog), a new autosomal recessive mutation in mice, has been mapped to the central ...
<p>Macroscopic views of thyroid glands from 12-week-old C.RF-Tshr<sup>wild/wild</sup> (a) and Tshr<s...
Abstract Background Pendred syndrome (PDS) is an autosomal recessive disorder characterized by senso...
<p>A) Representative cross-sections of thyroid glands of BC-<i>Tpst2<sup>grt</sup></i> mice at 10 we...
<b><i>Background:</i></b> Thyroid hemiagenesis, a rare congenital condition detected by ultrasound s...
Abstract. Thyroid carcinomas are the most common endocrine neoplasms in humans, with a globally incr...
Congenital hypothyroidism is a genetic condition in which the thyroid gland fails to produce suffici...
Graves ’ disease (GD) is an autoimmune condition in which goitre and hyperthyroidism are induced by ...
Graves' disease is characterized by overstimulation of the thyroid gland with agonistic autoantibodi...
Graves’ disease is the most common form of autoimmune thyroid disorder, characterized by hyperthyroi...
Background: Mutations in the SLC26A4 gene, coding for the anion transporter pendrin, are responsible...
Gene targeting technology has allowed the generation of mouse mutants which lack specific genes. The...
We have investigated thyroid structure and function in mice homozygous for the chromosome 15 mutatio...
Unless treated, congenital hypothyroidism causes severe mental retardation, stunted physical develop...
The NOD mouse, an ideal model for insulin-dependent diabetes mellitus, is also useful to study the p...
Congenital goiter (cog), a new autosomal recessive mutation in mice, has been mapped to the central ...
<p>Macroscopic views of thyroid glands from 12-week-old C.RF-Tshr<sup>wild/wild</sup> (a) and Tshr<s...
Abstract Background Pendred syndrome (PDS) is an autosomal recessive disorder characterized by senso...
<p>A) Representative cross-sections of thyroid glands of BC-<i>Tpst2<sup>grt</sup></i> mice at 10 we...
<b><i>Background:</i></b> Thyroid hemiagenesis, a rare congenital condition detected by ultrasound s...
Abstract. Thyroid carcinomas are the most common endocrine neoplasms in humans, with a globally incr...
Congenital hypothyroidism is a genetic condition in which the thyroid gland fails to produce suffici...
Graves ’ disease (GD) is an autoimmune condition in which goitre and hyperthyroidism are induced by ...
Graves' disease is characterized by overstimulation of the thyroid gland with agonistic autoantibodi...
Graves’ disease is the most common form of autoimmune thyroid disorder, characterized by hyperthyroi...
Background: Mutations in the SLC26A4 gene, coding for the anion transporter pendrin, are responsible...