(Q35145159)

6 August 2017

1 reference

title

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

1 reference

6 August 2017

0 references

1

G Van Vliet

1 reference

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

1 reference

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

6 August 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

Lingual thyroid and hyperthyroidism: a new case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

Transcription factor haploinsufficiency: when half a loaf is not enough

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

Frequency and characteristics of lingual thyroid not detected by screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

Treatment of congenital hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Neonatal hypothyroidism: treatment and outcome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Probing the cause of thyroid dysgenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Genetic regulation of thyroid development

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Thyrotoxicosis in a patient with submandibular thyroid

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Ectopic lingual thyroid masquerading as thyroid cancer metastases

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Thyroid dysgenesis in monozygotic twins: variants identified by scintigraphy.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Recent advances in understanding the molecular basis of primary congenital hypothyroidism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Ectopic lingual thyroid as unusual cause of severe dysphagia.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Secretion of hormones by ectopic thyroid glands after prolonged thyroxine therapy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

A unique combination of transcription factors controls differentiation of thyroid cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

A mouse model for hereditary thyroid dysgenesis and cleft palate

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Congenital hypothyroidism, spiky hair, and cleft palate

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Congenital hypothyroidism: increased incidence in Asian families

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Radionuclide Imaging in Primary Permanent Congenital Hypothyroidism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Twinning: mechanisms and genetic implications

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

Cellular patterning of the vertebrate embryo

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00107.X

7 January 2021

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