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| 1 | Valsartan, a potent, orally active angiotensin II antagonist developed from the structurally new amino acid series 显示文摘 | Buhlmayer P Furet P Criscione L | 1994 | Bioorg Med Chem Lett1994，4，1： | 1 |
| 2 | Anthranilic acidamides:a novel class of antiangiogenic VEGF receptor kinase inhibitors 显示文摘 | MANLEY PW FURET P BOLD G | 2002 | J Med Chem2002，45，26： | 1 |
| 3 | Imidazo 显示文摘 | Stauffer F Maira SM Furet P | 2008 | Bioorg Med Cbem Lett2008，18，3： | 1 |
| 4 | Inhibition of cyclindependent kinase 4 (Cdk4) by fascaplysin, a marine natural product 显示文摘 | Soni R Muller L Furet P | 2000 | Biochem Biopbys Res Commun2000，275，： | 1 |
| 5 | Structure-based design and synthesis of high affinity tripeptide ligands of the Grb2-SH2 domain 显示文摘 | Furet P Gay B Caravatti G | 1998 | J Med Chem1998，41，18： | 1 |
| 6 | Molecular quantification of lactic acid bacteria in fermented milk products using real-time quantitative PCR显示文摘 | FURET J P QUNE P TAILLIEZ P | 2004 | International Journal of Food Microbiology2004，97，2： | 1 |
| 7 | New aro- matase inhibitors from the 3-pyridyl arylether and l-aryl pyrrolo pyridine series显示文摘 | STAUFFER F FURET P FLOERSHEIMER A | 2012 | Bioorg Med Chem Lett2012，22，5： | 1 |
| 8 | CGP 79787D (PTK787/ZK22 2584), CGP 84738 NVP-AAC789, NVP-AAD777 and relat- ed 1-anilino-(4-pyridylmethyl)phthalazines as inhibitors of VEGF- and bFGF-indueed angiogenesis 显示文摘 | Bold G Frei J Furet P | 2002 | Cancer Res2002，27，1： | 1 |
| 9 | Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia显示文摘 | Cools J Mentens N Furet P | 2004 | Cancer Res2004，64，18： | 1 |
| 10 | Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors 显示文摘 | Manley PW Furet P Bold G | 2002 | Med Chem2002，45，26： | 1 |
| 11 | Molecular quantification of lactic acid bacteria in fermented milk products using real-time quantitative PCR显示文摘 | FURET J P QUENEE P TAILLIEZ P | 2004 | International Journal of Food Microbiology2004，97，2： | 1 |
| 12 | Inhibition of cyclin-dependent kinase 4 (CDK4) by fascaplyisn, a marine natural product显示文摘 | SONI R MULLER L FURET P | 2000 | Biochem Biophys Res Commun2000，275，3： | 1 |
| 13 | Analysis of genetic relationships between 10 cattle breeds with 17 microsatellites显示文摘 | Moazami-Guodarzi K Laloe D Furet J P | 1997 | Animal Genetics1997，28，： | 1 |
| 14 | Imidazo quinolines as inhibitors of the PI3K/PKB - pathway 显示文摘 | Stauffer F Maira SM Furet P | 2008 | Bioorg Med Chem Lett2008，18，3： | 1 |
| 15 | 4-(Phenylamino) pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinase显示文摘 | Traxler P Furet P Mett H | 1996 | J Med Chem1996，39，12： | 1 |
| 16 | Estimation of pig fecal contami- nation in a river catchment by real-time PCR using two pig-specific Bacteroidales 16S rRNA genetic markers显示文摘 | Mieszkin S Furet J P Corthier G | 2009 | Applied and Environ- mental Microbiology2009，75，10： | 1 |
| 17 | The gene encoding as αs1-casein is expressed in human mammary epithelial cells during lactation显示文摘 | Martin P Brignon G Furet J P | 1996 | Lait1996，，76： | 1 |
| 18 | Quantitative effects of an intronic retroviral insertion on the transcription of the ty- rosinas gene in recessive white chickens显示文摘 | Chang C M Furet J P Coville J I | 2007 | Animal Genetics2007，38，2： | 1 |
| 19 | 2,6,9-Trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors 显示文摘 | Imbach P Capraro HG Furet P | 1999 | Bioorg Med Chem Lett1999，9，1： | 1 |
| 20 | Discovery of 3-(2,6-di- chloro-3, 5-dimethoxy-phenyl )-l-I 6--pyrimidin-4-yl t-1-methyl-urea ( NVP- BGJ398) , a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase 显示文摘 | Guagnano V Furet P Spanka C | 2011 | J Med Chem2011，54，： | 1 |
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