(Q28369425)

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Stability-activity relationships of a family of G-tetrad forming oligonucleotides as potent HIV inhibitors. A basis for anti-HIV drug design

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Stability-activity relationships of a family of G-tetrad forming oligonucleotides as potent HIV inhibitors. A basis for anti-HIV drug design (English)

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2

object named as

E De Clercq

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author name string

N Jing

1

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R F Rando

3

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L Pallansch

4

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C Lackman-Smith

5

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S Lee

6

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M E Hogan

7

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language of work or name

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publication date

4 February 2000

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Journal of Biological Chemistry

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275

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5

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3421-30

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Suppression of human immunodeficiency virus type 1 activity in vitro by oligonucleotides which form intramolecular tetrads

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Ion Selective Folding of Loop Domains in a Potent Anti-HIV Oligonucleotide

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A DNA aptamer which binds to and inhibits thrombin exhibits a new structural motif for DNA.

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The retroviral enzymes

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Solution structure of the N-terminal zinc binding domain of HIV-1 integrase

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Solution structure of the DNA binding domain of HIV-1 integrase

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The DNA-binding domain of HIV-1 integrase has an SH3-like fold

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10.1074/JBC.275.5.3421

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release_wpda4rmn5zfyzfijoo45g6pmp4

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