AI54340/AI/NIAID NIH HHS/United States[Grants and Funding] - Search Results

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2005	1
2007	2
2025	0

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Manipulation of P-TEFb control machinery by HIV: recruitment of P-TEFb from the large form by Tat and binding of HEXIM1 to TAR.

Sedore SC, Byers SA, Biglione S, Price JP, Maury WJ, Price DH. Sedore SC, et al. Nucleic Acids Res. 2007;35(13):4347-58. doi: 10.1093/nar/gkm443. Epub 2007 Jun 18. Nucleic Acids Res. 2007. PMID: 17576689 Free PMC article.

Analysis of the large inactive P-TEFb complex indicates that it contains one 7SK molecule, a dimer of HEXIM1 or HEXIM2, and two P-TEFb molecules containing Cdk9 phosphorylated at threonine 186.

Li Q, Price JP, Byers SA, Cheng D, Peng J, Price DH. Li Q, et al. J Biol Chem. 2005 Aug 5;280(31):28819-26. doi: 10.1074/jbc.M502712200. Epub 2005 Jun 17. J Biol Chem. 2005. PMID: 15965233 Free article.

Inhibition of HIV-1 replication by P-TEFb inhibitors DRB, seliciclib and flavopiridol correlates with release of free P-TEFb from the large, inactive form of the complex.

Biglione S, Byers SA, Price JP, Nguyen VT, Bensaude O, Price DH, Maury W. Biglione S, et al. Retrovirology. 2007 Jul 11;4:47. doi: 10.1186/1742-4690-4-47. Retrovirology. 2007. PMID: 17625008 Free PMC article.

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