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Items: 1 to 20 of 575

1.

Widespread use of TATA elements in the core promoters for RNA polymerases III, II, and I in fission yeast.

Hamada M, Huang Y, Lowe TM, Maraia RJ.

Mol Cell Biol. 2001 Oct;21(20):6870-81.

3.

The fission yeast TFIIB-related factor limits RNA polymerase III to a TATA-dependent pathway of TBP recruitment.

Huang Y, McGillicuddy E, Weindel M, Dong S, Maraia RJ.

Nucleic Acids Res. 2003 Apr 15;31(8):2108-16.

4.

Comparison of the RNA polymerase III transcription machinery in Schizosaccharomyces pombe, Saccharomyces cerevisiae and human.

Huang Y, Maraia RJ.

Nucleic Acids Res. 2001 Jul 1;29(13):2675-90. Review. Erratum in: Nucleic Acids Res 2001 Aug 15;29(16):2.

5.

The N-terminal domain of the human TATA-binding protein plays a role in transcription from TATA-containing RNA polymerase II and III promoters.

Lescure A, Lutz Y, Eberhard D, Jacq X, Krol A, Grummt I, Davidson I, Chambon P, Tora L.

EMBO J. 1994 Mar 1;13(5):1166-75.

6.

Differential mode of TBP utilization in transcription of the tRNA[Ser]Sec gene and TATA-less class III genes.

Park JM, Lee JY, Hatfield DL, Lee BJ.

Gene. 1997 Sep 1;196(1-2):99-103.

PMID:
9322746
10.
11.

The symmetry of the yeast U6 RNA gene's TATA box and the orientation of the TATA-binding protein in yeast TFIIIB.

Whitehall SK, Kassavetis GA, Geiduschek EP.

Genes Dev. 1995 Dec 1;9(23):2974-85.

12.

TFIIIC-independent in vitro transcription of yeast tRNA genes.

Dieci G, Percudani R, Giuliodori S, Bottarelli L, Ottonello S.

J Mol Biol. 2000 Jun 9;299(3):601-13.

PMID:
10835271
14.
15.

RNA polymerase II/III transcription specificity determined by TATA box orientation.

Wang Y, Stumph WE.

Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8606-10.

16.

hTFIIIB-beta stably binds to pol II promoters and recruits RNA polymerase III in a hTFIIIC1 dependent way.

Kober I, Teichmann M, Seifart KH.

J Mol Biol. 1998 Nov 20;284(1):7-20.

PMID:
9811538
17.

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