| Year |
Citation |
Score |
| 2012 |
Vaidya AS, Neelarapu R, Madriaga A, Bai H, Mendonca E, Abdelkarim H, van Breemen RB, Blond SY, Petukhov PA. Novel histone deacetylase 8 ligands without a zinc chelating group: exploring an 'upside-down' binding pose. Bioorganic & Medicinal Chemistry Letters. 22: 6621-7. PMID 23010266 DOI: 10.1016/J.Bmcl.2012.08.104 |
0.306 |
|
| 2011 |
Neelarapu R, Holzle DL, Velaparthi S, Bai H, Brunsteiner M, Blond SY, Petukhov PA. Design, synthesis, docking, and biological evaluation of novel diazide-containing isoxazole- and pyrazole-based histone deacetylase probes. Journal of Medicinal Chemistry. 54: 4350-64. PMID 21548582 DOI: 10.1021/Jm2001025 |
0.701 |
|
| 2009 |
He B, Velaparthi S, Pieffet G, Pennington C, Mahesh A, Holzle DL, Brunsteiner M, van Breemen R, Blond SY, Petukhov PA. Binding ensemble profiling with photoaffinity labeling (BEProFL) approach: mapping the binding poses of HDAC8 inhibitors. Journal of Medicinal Chemistry. 52: 7003-13. PMID 19886628 DOI: 10.1021/Jm9005077 |
0.7 |
|
| 2009 |
Kim KH, Gaisina I, Gallier F, Holzle D, Blond SY, Mesecar A, Kozikowski AP. Use of molecular modeling, docking, and 3D-QSAR studies for the determination of the binding mode of benzofuran-3-yl-(indol-3-yl) maleimides as GSK-3β inhibitors Journal of Molecular Modeling. 15: 1463-1479. PMID 19440740 DOI: 10.1007/S00894-009-0498-X |
0.699 |
|
| 2009 |
Gaisina IN, Gallier F, Ougolkov AV, Kim KH, Kurome T, Guo S, Holzle D, Luchini DN, Blond SY, Billadeau DD, Kozikowski AP. From a natural product lead to the identification of potent and selective benzofuran-3-yl-(indol-3-yl)maleimides as glycogen synthase kinase 3βinhibitors that suppress proliferation and survival of pancreatic cancer cells Journal of Medicinal Chemistry. 52: 1853-1863. PMID 19338355 DOI: 10.1021/Jm801317H |
0.683 |
|
| 2008 |
Ravindran S, Narayanan K, Eapen AS, Hao J, Ramachandran A, Blond S, George A. Endoplasmic reticulum chaperone protein GRP-78 mediates endocytosis of dentin matrix protein 1. The Journal of Biological Chemistry. 283: 29658-70. PMID 18757373 DOI: 10.1074/Jbc.M800786200 |
0.378 |
|
| 2006 |
Lamb HK, Mee C, Xu W, Liu L, Blond S, Cooper A, Charles IG, Hawkins AR. The affinity of a major Ca2+ binding site on GRP78 is differentially enhanced by ADP and ATP. The Journal of Biological Chemistry. 281: 8796-805. PMID 16418174 DOI: 10.1074/Jbc.M503964200 |
0.351 |
|
| 2004 |
Kroczynska B, Evangelista CM, Samant SS, Elguindi EC, Blond SY. The SANT2 domain of the murine tumor cell DnaJ-like protein 1 human homologue interacts with alpha1-antichymotrypsin and kinetically interferes with its serpin inhibitory activity. The Journal of Biological Chemistry. 279: 11432-43. PMID 14668352 DOI: 10.1074/jbc.M310903200 |
0.312 |
|
| 2001 |
King LS, Berg M, Chevalier M, Carey A, Elguindi EC, Blond SY. Isolation, expression, and characterization of fully functional nontoxic BiP/GRP78 mutants. Protein Expression and Purification. 22: 148-58. PMID 11388813 DOI: 10.1006/Prep.2001.1424 |
0.652 |
|
| 2000 |
Chevalier M, Rhee H, Elguindi EC, Blond SY. Interaction of murine BiP/GRP78 with the DnaJ homologue MTJ1 Journal of Biological Chemistry. 275: 19620-19627. PMID 10777498 DOI: 10.1074/Jbc.M001333200 |
0.64 |
|
| 1999 |
King L, Chevalier M, Blond SY. Specificity of peptide-induced depolymerization of the recombinant carboxy-terminal fragment of BiP/GRP78 Biochemical and Biophysical Research Communications. 263: 181-186. PMID 10486274 DOI: 10.1006/Bbrc.1999.1321 |
0.656 |
|
| 1998 |
Chevalier M, King L, Wang C, Gething MJ, Elguindi E, Blond SY. Substrate binding induces depolymerization of the C-terminal peptide binding domain of murine GRP78/BiP. The Journal of Biological Chemistry. 273: 26827-35. PMID 9756927 DOI: 10.1074/Jbc.273.41.26827 |
0.666 |
|
| 1998 |
Chevalier M, King L, Blond S. Purification and properties of BiP Methods in Enzymology. 290: 384-409. PMID 9534177 DOI: 10.1016/S0076-6879(98)90033-7 |
0.658 |
|
| 1997 |
King L, Wang C, Blond S. Mutational analysis of the C-Terminal domain of the molecular chaperone BiP Faseb Journal. 11. |
0.33 |
|
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