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Items: 1 to 20 of 206

1.

Thyroid transcription factor 1 rescues PAX8/p300 synergism impaired by a natural PAX8 paired domain mutation with dominant negative activity.

Grasberger H, Ringkananont U, Lefrancois P, Abramowicz M, Vassart G, Refetoff S.

Mol Endocrinol. 2005 Jul;19(7):1779-91. Epub 2005 Feb 17.

PMID:
15718293
2.

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

Di Palma T, Nitsch R, Mascia A, Nitsch L, Di Lauro R, Zannini M.

J Biol Chem. 2003 Jan 31;278(5):3395-402. Epub 2002 Nov 18.

3.

TAZ is a coactivator for Pax8 and TTF-1, two transcription factors involved in thyroid differentiation.

Di Palma T, D'Andrea B, Liguori GL, Liguoro A, de Cristofaro T, Del Prete D, Pappalardo A, Mascia A, Zannini M.

Exp Cell Res. 2009 Jan 15;315(2):162-75. doi: 10.1016/j.yexcr.2008.10.016. Epub 2008 Oct 28.

PMID:
19010321
4.

Genetic analysis of the PAX8 gene in children with congenital hypothyroidism and dysgenetic or eutopic thyroid glands: identification of a novel sequence variant.

Tonacchera M, Banco ME, Montanelli L, Di Cosmo C, Agretti P, De Marco G, Ferrarini E, Ordookhani A, Perri A, Chiovato L, Santini F, Vitti P, Pinchera A.

Clin Endocrinol (Oxf). 2007 Jul;67(1):34-40. Epub 2007 Apr 15.

PMID:
17437516
5.

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

Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Medeiros-Neto G, Kopp P.

J Clin Endocrinol Metab. 2001 Aug;86(8):3962-7.

PMID:
11502839
6.

Determination of functional domains of the human transcription factor PAX8 responsible for its nuclear localization and transactivating potential.

Poleev A, Okladnova O, Musti AM, Schneider S, Royer-Pokora B, Plachov D.

Eur J Biochem. 1997 Aug 1;247(3):860-9.

7.

Tumor necrosis factor-alpha regulation of thyroid transcription factor-1 and Pax-8 in rat thyroid FRTL-5 cells.

Ohmori M, Harii N, Endo T, Onaya T.

Endocrinology. 1999 Oct;140(10):4651-8.

PMID:
10499522
8.

Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid.

Meeus L, Gilbert B, Rydlewski C, Parma J, Roussie AL, Abramowicz M, Vilain C, Christophe D, Costagliola S, Vassart G.

J Clin Endocrinol Metab. 2004 Sep;89(9):4285-91.

PMID:
15356023
9.

The thyroid transcription factor 2 (TTF-2) is a promoter-specific DNA-binding independent transcriptional repressor.

Perrone L, Pasca di Magliano M, Zannini M, Di Lauro R.

Biochem Biophys Res Commun. 2000 Aug 18;275(1):203-8.

PMID:
10944465
10.

Pax8 has a key role in thyroid cell differentiation.

Pasca di Magliano M, Di Lauro R, Zannini M.

Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13144-9.

12.

Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8.

Vilain C, Rydlewski C, Duprez L, Heinrichs C, Abramowicz M, Malvaux P, Renneboog B, Parma J, Costagliola S, Vassart G.

J Clin Endocrinol Metab. 2001 Jan;86(1):234-8.

PMID:
11232006
13.

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

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

Hum Mol Genet. 2009 Jun 15;18(12):2266-76. doi: 10.1093/hmg/ddp162. Epub 2009 Mar 31.

PMID:
19336474
14.

Effects of Pax8 and TTF-1 thyroid transcription factor gene transfer in hepatoma cells: imaging of functional protein-protein interaction and iodide uptake.

Altmann A, Schulz RB, Glensch G, Eskerski H, Zitzmann S, Eisenhut M, Haberkorn U.

J Nucl Med. 2005 May;46(5):831-9.

15.

Thyroid transcription factor 1 and Pax8 synergistically activate the promoter of the human thyroglobulin gene.

Espinoza CR, Schmitt TL, Loos U.

J Mol Endocrinol. 2001 Aug;27(1):59-67.

PMID:
11463576
16.

Familial PAX8 small deletion (c.989_992delACCC) associated with extreme phenotype variability.

de Sanctis L, Corrias A, Romagnolo D, Di Palma T, Biava A, Borgarello G, Gianino P, Silvestro L, Zannini M, Dianzani I.

J Clin Endocrinol Metab. 2004 Nov;89(11):5669-74.

PMID:
15531527
18.

Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.

Vincenzi M, Camilot M, Ferrarini E, Teofoli F, Venturi G, Gaudino R, Cavarzere P, De Marco G, Agretti P, Dimida A, Tonacchera M, Boner A, Antoniazzi F.

BMC Endocr Disord. 2014 Aug 22;14:69. doi: 10.1186/1472-6823-14-69.

19.

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

Van Vliet G.

Clin Genet. 2003 Jun;63(6):445-55. Review.

PMID:
12786749
20.

Thyroid-specific gene expression is differentially influenced by intracellular glutathione level in FRTL-5 cells.

Lonigro R, Donnini D, Fabbro D, Perrella G, Damante G, Ambesi Impiombato FS, Curcio F.

Endocrinology. 2000 Mar;141(3):901-9.

PMID:
10698164

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