(Q28585755)

31 January 2017

title

Perturbed thyroid morphology and transient hypothyroidism symptoms in Hoxa5 mutant mice (English)

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31 January 2017

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GOA release 2020-03-11

author name string

Dominique Meunier

series ordinal

1

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31 January 2017

Josée Aubin

series ordinal

2

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31 January 2017

Lucie Jeannotte

series ordinal

3

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31 January 2017

publication date

1 July 2003

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31 January 2017

published in

Developmental Dynamics

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31 January 2017

volume

227

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31 January 2017

issue

3

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31 January 2017

page(s)

367–378

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Evaluation and characterization of the hypothyroid hyt/hyt mouse. I: Somatic and behavioral studies

31 January 2017

cites work

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Early postnatal lethality in Hoxa-5 mutant mice is attributable to respiratory tract defects

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Loss of Hoxa5 gene function in mice perturbs intestinal maturation

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Cooperation of Hoxa5 and Pax1 genes during formation of the pectoral girdle

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Inherited primary hypothyroidism in mice

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Paralogous mouse Hox genes, Hoxa9, Hoxb9, and Hoxd9, function together to control development of the mammary gland in response to pregnancy

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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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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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Redundant Domains Contribute to the Transcriptional Activity of the Thyroid Transcription Factor 1

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Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure

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Pax8 has a key role in thyroid cell differentiation

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7 January 2021

No milk today (my Hox have gone away).

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7 January 2021

Pax-8 protein levels regulate thyroglobulin gene expression

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7 January 2021

Differential mammary morphogenesis along the anteroposterior axis in Hoxc6 gene targeted mice

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Hoxc13 mutant mice lack external hair

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A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats

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Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure

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7 January 2021

Specification of axial identity in the mouse: role of the Hoxa-5 (Hox1.3) gene

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7 January 2021

A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases

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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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7 January 2021

Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands

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7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

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7 January 2021

Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones

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7 January 2021

Effects of maternal hypothyroidism on the weight and thyroid hormone content of rat embryonic tissues, before and after onset of fetal thyroid function

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7 January 2021

The paired-domain transcription factor Pax8 binds to the upstream enhancer of the rat sodium/iodide symporter gene and participates in both thyroid-specific and cyclic-AMP-dependent transcription

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7 January 2021

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7 January 2021

Checklist: vertebrate homeobox genes

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7 January 2021

Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis

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7 January 2021

Specific Ablation of Thyroid Follicle Cells in Adult Transgenic Mice*

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7 January 2021

Consequences of thyroid hormone deficiency induced by the specific ablation of thyroid follicle cells in adult transgenic mice

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7 January 2021

Effects of perinatal thyroid hormone deprivation on the growth and behaviour of newborn mice

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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

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7 January 2021

Identifiers

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31 January 2017

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