De Francesco R - Search Results

1

A functionally orthogonal estrogen receptor-based transcription switch specifically induced by a nonsteroid synthetic ligand.

Gallinari P, Lahm A, Koch U, Paolini C, Nardi MC, Roscilli G, Kinzel O, Fattori D, Muraglia E, Toniatti C, Cortese R, De Francesco R, Ciliberto G. Gallinari P, et al. Among authors: de francesco r. Chem Biol. 2005 Aug;12(8):883-93. doi: 10.1016/j.chembiol.2005.05.018. Chem Biol. 2005. PMID: 16125100 Free article.

2

Tomei L, Cortese R, De Francesco R. Tomei L, et al. Among authors: de francesco r. EMBO J. 1992 Nov;11(11):4119-29. doi: 10.1002/j.1460-2075.1992.tb05505.x. EMBO J. 1992. PMID: 1356766 Free PMC article.

3

Circular dichroism study on the conformational stability of the dimerization domain of transcription factor LFB1.

De Francesco R, Pastore A, Vecchio G, Cortese R. De Francesco R, et al. Biochemistry. 1991 Jan 8;30(1):143-7. doi: 10.1021/bi00215a021. Biochemistry. 1991. PMID: 1988015

4

LFB1/HNF1 acts as a repressor of its own transcription.

Piaggio G, Tomei L, Toniatti C, De Francesco R, Gerstner J, Cortese R. Piaggio G, et al. Among authors: de francesco r. Nucleic Acids Res. 1994 Oct 11;22(20):4284-90. doi: 10.1093/nar/22.20.4284. Nucleic Acids Res. 1994. PMID: 7937157 Free PMC article.

5

A zinc binding site in viral serine proteinases.

De Francesco R, Urbani A, Nardi MC, Tomei L, Steinkühler C, Tramontano A. De Francesco R, et al. Biochemistry. 1996 Oct 15;35(41):13282-7. doi: 10.1021/bi9616458. Biochemistry. 1996. PMID: 8873593

6

Affinity selection of a camelized V(H) domain antibody inhibitor of hepatitis C virus NS3 protease.

Martin F, Volpari C, Steinkuhler C, Dimasi N, Brunetti M, Biasiol G, Altamura S, Cortese R, De Francesco R, Sollazzo M. Martin F, et al. Among authors: de francesco r. Protein Eng. 1997 May;10(5):607-14. doi: 10.1093/protein/10.5.607. Protein Eng. 1997. PMID: 9215580

7

The nonstructural proteins of the hepatitis C virus: structure and functions.

Neddermann P, Tomei L, Steinkühler C, Gallinari P, Tramontano A, De Francesco R. Neddermann P, et al. Among authors: de francesco r. Biol Chem. 1997 Jun;378(6):469-76. Biol Chem. 1997. PMID: 9224925 Review.

8

Characterization of engineered hepatitis C virus NS3 protease inhibitors affinity selected from human pancreatic secretory trypsin inhibitor and minibody repertoires.

Dimasi N, Martin F, Volpari C, Brunetti M, Biasiol G, Altamura S, Cortese R, De Francesco R, Steinkühler C, Sollazzo M. Dimasi N, et al. Among authors: de francesco r. J Virol. 1997 Oct;71(10):7461-9. doi: 10.1128/JVI.71.10.7461-7469.1997. J Virol. 1997. PMID: 9311825 Free PMC article.

9

Product inhibition of the hepatitis C virus NS3 protease.

Steinkühler C, Biasiol G, Brunetti M, Urbani A, Koch U, Cortese R, Pessi A, De Francesco R. Steinkühler C, et al. Among authors: de francesco r. Biochemistry. 1998 Jun 23;37(25):8899-905. doi: 10.1021/bi980313v. Biochemistry. 1998. PMID: 9636031

10

Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimizing the cleavage products.

Ingallinella P, Altamura S, Bianchi E, Taliani M, Ingenito R, Cortese R, De Francesco R, Steinkühler C, Pessi A. Ingallinella P, et al. Among authors: de francesco r. Biochemistry. 1998 Jun 23;37(25):8906-14. doi: 10.1021/bi980314n. Biochemistry. 1998. PMID: 9636032

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