Development of the thyroid gland: lessons from congenitally hypothyroid mice and men. (Q35145159)

6 August 2017

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title

Development of the thyroid gland: lessons from congenitally hypothyroid mice and men. (English)

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6 August 2017

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1

G Van Vliet

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6 August 2017

1 June 2003

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6 August 2017

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6 August 2017

63

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6 August 2017

6

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6 August 2017

445-455

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Contribution of thyroid ultrasound and serum calcitonin to the diagnosis of congenital hypothyroidism

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Frequency and characteristics of lingual thyroid not detected by screening

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Treatment of congenital hypothyroidism

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Congenital central isolated hypothyroidism caused by a homozygous mutation in the TSH-beta subunit gene

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Probing the cause of thyroid dysgenesis

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Genetic regulation of thyroid development

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Additional phenotypic abnormalities with presence of cysts within the empty thyroid area in patients with congenital hypothyroidism with thyroid dysgenesis.

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Thyrotoxicosis in a patient with submandibular thyroid

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A search for the possible molecular mechanisms of thyroid dysgenesis: sex ratios and associated malformations

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Ectopic lingual thyroid masquerading as thyroid cancer metastases

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Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidism

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Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland

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Thyroid dysgenesis in monozygotic twins: variants identified by scintigraphy.

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Recent advances in understanding the molecular basis of primary congenital hypothyroidism

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Ectopic lingual thyroid as unusual cause of severe dysphagia.

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Ectopic thyroid: residual function after withdrawal of treatment in infancy and later childhood

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Secretion of hormones by ectopic thyroid glands after prolonged thyroxine therapy

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Primary ectopic thyroid papillary carcinoma in the floor of the mouth and tongue: a case report

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A unique combination of transcription factors controls differentiation of thyroid cells

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TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

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The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

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Thyroid-specific enhancer-binding protein/thyroid transcription factor 1 is not required for the initial specification of the thyroid and lung primordia.

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Distribution of the titf2/foxe1 gene product is consistent with an important role in the development of foregut endoderm, palate, and hair.

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A mouse model for hereditary thyroid dysgenesis and cleft palate

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Follicular cells of the thyroid gland require Pax8 gene function

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The paired domain-containing factor Pax8 and the homeodomain-containing factor TTF-1 directly interact and synergistically activate transcription

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Role of the thyroid-stimulating hormone receptor signaling in development and differentiation of the thyroid gland

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Defining thyrotropin-dependent and -independent steps of thyroid hormone synthesis by using thyrotropin receptor-null mice

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Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors

1 reference

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PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

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Congenital hypothyroidism, spiky hair, and cleft palate

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Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

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A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

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A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child

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Thyroid dysgenesis caused by PAX8 mutation: the hypermutability with CpG dinucleotides at codon 31.

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Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene

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The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor

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A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene

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Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

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Congenital hypothyroidism: increased incidence in Asian families

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The hypothalamic-pituitary-thyroid negative feedback control axis in children with treated congenital hypothyroidism

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Radionuclide Imaging in Primary Permanent Congenital Hypothyroidism

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Diabetic embryopathy in C57BL/6J mice. Altered fetal sex ratio and impact of the splotch allele

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Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology.

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Twinning: mechanisms and genetic implications

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Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

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Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

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Clonal origin of non-medullary thyroid tumours assessed by non-random X-chromosome inactivation

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Cellular patterning of the vertebrate embryo

1 reference

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10.1034/J.1399-0004.2003.00107.X

Identifiers

DOI

1 reference

release_ovfj2xfzubajnmmhr75gvymppu

6 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ovfj2xfzubajnmmhr75gvymppu

24 November 2022

mapped directly with Wikidata item

PubMed ID

12786749

1 reference

PubMed ID

12786749