A mouse model for hereditary thyroid dysgenesis and cleft palate (Q28513528)

25 January 2017

title

A mouse model for hereditary thyroid dysgenesis and cleft palate (English)

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25 January 2017

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GOA release 2020-03-11

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C. Arra

5

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Hans Schöler

object named as

H. Schöler

10

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author name string

M. De Felice

1

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25 January 2017

C. Ovitt

2

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E. Biffali

3

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A. Rodriguez-Mallon

4

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K. Anastassiadis

6

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P. E. Macchia

7

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M. G. Mattei

8

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A. Mariano

9

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V. Macchia

11

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R. Di Lauro

12

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25 January 2017

language of work or name

English

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publication date

1 August 1998

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25 January 2017

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25 January 2017

volume

19

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issue

4

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page(s)

395–398

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Comparison of Epidemiological Data on Congenital Hypothyroidism in Europe with Those of Other Parts in the World

25 January 2017

cites work

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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

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

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7 January 2021

Thyroid-specific gene expression

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7 January 2021

Thyroid Development and Disorders of Thyroid Function in the Newborn

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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

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7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

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7 January 2021

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

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7 January 2021

Transforming growth factor-beta 3 is required for secondary palate fusion

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7 January 2021

Congenital hypothyroidism, spiky hair, and cleft palate

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7 January 2021

Syndromic association of cleft palate, bilateral choanal atresia, curly hair, and congenital hypothyroidism

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7 January 2021

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

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7 January 2021

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

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7 January 2021

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

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7 January 2021

Gene targeting in embryonic stem cells

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7 January 2021

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

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7 January 2021