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Renaud Prudent
Renaud Prudent
Scientific Director Biochemistry
在 edelris.com 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Identification of polyoxometalates as nanomolar noncompetitive inhibitors of protein kinase CK2
R Prudent, V Moucadel, B Laudet, C Barette, L Lafanechère, ...
Chemistry & biology 15 (7), 683-692, 2008
1972008
New protein kinase CK2 inhibitors: jumping out of the catalytic box
R Prudent, C Cochet
Chemistry & biology 16 (2), 112-120, 2009
1322009
Structure-based design of small peptide inhibitors of protein kinase CK2 subunit interaction
B Laudet, C Barette, V Dulery, O Renaudet, P Dumy, A Metz, R Prudent, ...
Biochemical Journal 408 (3), 363-373, 2007
1132007
Functional analysis of the BMP9 response of ALK1 mutants from HHT2 patients: a diagnostic tool for novel ACVRL1 mutations
N Ricard, M Bidart, C Mallet, G Lesca, S Giraud, R Prudent, JJ Feige, ...
Blood, The Journal of the American Society of Hematology 116 (9), 1604-1612, 2010
972010
LIM kinases: cofilin and beyond
C Prunier, R Prudent, R Kapur, K Sadoul, L Lafanechère
Oncotarget 8 (25), 41749, 2017
942017
Antitumor activity of pyridocarbazole and benzopyridoindole derivatives that inhibit protein kinase CK2
R Prudent, V Moucadel, CH Nguyen, C Barette, F Schmidt, JC Florent, ...
Cancer research 70 (23), 9865-9874, 2010
912010
Pharmacological inhibition of LIM kinase stabilizes microtubules and inhibits neoplastic growth
R Prudent, E Vassal-Stermann, CH Nguyen, C Pillet, A Martinez, ...
Cancer research 72 (17), 4429-4439, 2012
832012
Identification of chemical inhibitors of protein-kinase CK2 subunit interaction
B Laudet, V Moucadel, R Prudent, O Filhol, YS Wong, D Royer, C Cochet
Molecular and cellular biochemistry 316, 63-69, 2008
832008
New potent dual inhibitors of CK2 and Pim kinases: discovery and structural insights
M López‐Ramos, R Prudent, V Moucadel, CF Sautel, C Barette, ...
The FASEB Journal 24 (9), 3171-3185, 2010
752010
Structure-based discovery of small molecules targeting different surfaces of protein-kinase CK2
R Prudent, CF Sautel, C Cochet
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1804 (3), 493-498, 2010
672010
Exploring new targets and chemical space with affinity selection-mass spectrometry
R Prudent, DA Annis, PJ Dandliker, JY Ortholand, D Roche
Nature Reviews Chemistry 5 (1), 62-71, 2021
662021
Functional Analysis of Protein Kinase CK2 of the Human Malaria Parasite Plasmodium falciparum
Z Holland, R Prudent, JB Reiser, C Cochet, C Doerig
Eukaryotic cell 8 (3), 388-397, 2009
602009
Antitumoral activity of allosteric inhibitors of protein kinase CK2
V Moucadel, R Prudent, CF Sautel, F Teillet, C Barette, L Lafanechere, ...
Oncotarget 2 (12), 997, 2011
522011
Expanding the chemical diversity of CK2 inhibitors
R Prudent, V Moucadel, M López-Ramos, S Aci, B Laudet, L Mouawad, ...
Molecular and cellular biochemistry 316, 71-85, 2008
452008
Azaindole derivatives are inhibitors of microtubule dynamics, with anti‐cancer and anti‐angiogenic activities
R Prudent, É Vassal‐Stermann, CH Nguyen, M Mollaret, J Viallet, ...
British journal of pharmacology 168 (3), 673-685, 2013
442013
LIM kinase inhibitor Pyr1 reduces the growth and metastatic load of breast cancers
C Prunier, V Josserand, J Vollaire, E Beerling, C Petropoulos, O Destaing, ...
Cancer Research 76 (12), 3541-3552, 2016
332016
Sulphamoylated 2-methoxyestradiol analogues induce apoptosis in adenocarcinoma cell lines
M Visagie, A Theron, T Mqoco, W Vieira, R Prudent, A Martinez, ...
PLoS One 8 (9), e71935, 2013
332013
Discovery of holoenzyme-disrupting chemicals as substrate-selective CK2 inhibitors
I Kufareva, B Bestgen, P Brear, R Prudent, B Laudet, V Moucadel, ...
Scientific reports 9 (1), 15893, 2019
222019
Novel in silico-designed estradiol analogues are cytotoxic to a multidrug-resistant cell line at nanomolar concentrations
A Theron, R Prudent, E Nolte, I van den Bout, R Punchoo, S Marais, ...
Cancer chemotherapy and pharmacology 75, 431-437, 2015
172015
Phosphorylation of the C subunit (p66) of human DNA polymerase δ
L Lemmens, S Urbach, R Prudent, C Cochet, G Baldacci, P Hughes
Biochemical and biophysical research communications 367 (2), 264-270, 2008
172008
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