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Items: 1 to 20 of 228

1.

TAF-like functions of human cytomegalovirus immediate-early proteins.

Lukac DM, Harel NY, Tanese N, Alwine JC.

J Virol. 1997 Oct;71(10):7227-39.

3.

TAF-like function of SV40 large T antigen.

Damania B, Alwine JC.

Genes Dev. 1996 Jun 1;10(11):1369-81.

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7.

Drosophila TAF(II)230 and the transcriptional activator VP16 bind competitively to the TATA box-binding domain of the TATA box-binding protein.

Nishikawa J, Kokubo T, Horikoshi M, Roeder RG, Nakatani Y.

Proc Natl Acad Sci U S A. 1997 Jan 7;94(1):85-90.

9.

Artificial recruitment of Sp1 or TBP can replace the role of IE1 in the synergistic transactivation by IE1 and IE2.

Kim JM, Hong Y, Kim S.

Biochem Biophys Res Commun. 2000 Mar 16;269(2):302-8.

PMID:
10708547
10.

TAF(II)170 interacts with the concave surface of TATA-binding protein to inhibit its DNA binding activity.

Pereira LA, van der Knaap JA, van den Boom V, van den Heuvel FA, Timmers HT.

Mol Cell Biol. 2001 Nov;21(21):7523-34.

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Mechanisms of transcriptional activation and repression can both involve TFIID.

Manley JL, Um M, Li C, Ashali H.

Philos Trans R Soc Lond B Biol Sci. 1996 Apr 29;351(1339):517-26. Review.

PMID:
8735274
16.

Two novel Drosophila TAF(II)s have homology with human TAF(II)30 and are differentially regulated during development.

Georgieva S, Kirschner DB, Jagla T, Nabirochkina E, Hanke S, Schenkel H, de Lorenzo C, Sinha P, Jagla K, Mechler B, Tora L.

Mol Cell Biol. 2000 Mar;20(5):1639-48.

20.

Potential targets for HSF1 within the preinitiation complex.

Yuan CX, Gurley WB.

Cell Stress Chaperones. 2000 Jul;5(3):229-42.

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