Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case-Reference-Cited by-同舟云学术

Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

Published:2009-03-31 Issue:12 Volume:18 Page:2266-2276
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Carre A.,Szinnai G.,Castanet M.,Sura-Trueba S.,Tron E.,Broutin-L'Hermite I.,Barat P.,Goizet C.,Lacombe D.,Moutard M.-L.,Raybaud C.,Raynaud-Ravni C.,Romana S.,Ythier H.,Leger J.,Polak M.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/12/2266/1813206/ddp162.pdf

Reference54 articles.

1. A thyroid-specific nuclear protein essential for tissue-specific expression of the thyroglobulin promoter.

2. Thyroid nuclear factor 1 (TTF-1) contains a homeodomain and displays a novel DNA binding specificity.

3. PAX8,TITF1, andFOXE1Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations

4. Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus

5. Pendrin Is a Novel In Vivo Downstream Target Gene of the TTF-1/Nkx-2.1 Homeodomain Transcription Factor in Differentiated Thyroid Cells

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