Structure-based drug design: From nucleic acid to membrane protein targets-Reference-Cited by-同舟云学术

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Structure-based drug design: From nucleic acid to membrane protein targets

Published:2009-06 Issue:3 Volume:86 Page:141-150
ISSN:0014-4800
Container-title:Experimental and Molecular Pathology
language:en
Short-container-title:Experimental and Molecular Pathology

Author:

Dailey Magdalena M.,Hait Chayanendu,Holt Patrick A.,Maguire Jon M.,Meier Jason B.,Miller M. Clarke,Petraccone Luigi,Trent John O.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Molecular Biology,Pathology and Forensic Medicine

Reference85 articles.

1. ISO-1 binding to the tautomerase active site of MIF inhibits its pro-inflammatory activity and increases survival in severe sepsis;Al-Abed;J. Biol. Chem.,2005

2. Solution structure of the two N-terminal RNA-binding domains of nucleolin and NMR study of the interaction with its RNA target;Allain;J. Mol. Biol.,2000

3. The chemokine SDF1 regulates migration of dentate granule cells;Bagri;Development,2002

4. Critical role for polar residues in coupling leukotriene B4 binding to signal transduction in BLT1;Basu;J. Biol. Chem.,2007

5. Antiproliferative activity of G-rich oligonucleotides correlates with protein binding;Bates;J. Biol. Chem.,1999

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