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3. Supplementary Figure 4 from Meriolins, a New Class of Cell Death–Inducing Kinase Inhibitors with Enhanced Selectivity for Cyclin-Dependent Kinases

4. Methods and Materials, Figure 4 Legend from Meriolins, a New Class of Cell Death–Inducing Kinase Inhibitors with Enhanced Selectivity for Cyclin-Dependent Kinases

5. Data from Meriolins, a New Class of Cell Death–Inducing Kinase Inhibitors with Enhanced Selectivity for Cyclin-Dependent Kinases

10. Monodisperse polysarcosine-based highly-loaded antibody-drug conjugates† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c9sc00285e

26. Correction: Characterization of Transglutaminase 2 activity inhibitors in monocytes in vitro and their effect in a mouse model for multiple sclerosis

28. Targeting RNA structure in SMN2 reverses spinal muscular atrophy molecular phenotypes

32. Sur l'identité de la chaleur et de la lumière

33. Targeting RNA structure in SMN2 reverses spinal muscular atrophy molecular phenotypes

36. Hétérocycles azotés dérivés d’acides tétramiques et de pyrimidines comme nouveaux agents anti-infectieux : activité antipaludique et anti-pneumocystose

37. Récents développements pour la recherche de nouvelles molécules antipaludiques : hétérocycles azotés dérivés d’acides tétramiques et de pyrimidines

39. New 1-arylindoles based serotonin 5-HT7 entagonists. Synthesis and binding evaluation studies

40. Unexpected matrix interactions in liquid secondary ion mass spectrometry of two pyranosyl mercaptans

41. Synthesis of 2-, 3-, and 4-Substituted Pyrido[2,3-b]indoles by C-N, C-O, and C-C(sp) Bond Formation

43. Chemoselective functionalization of α-carbolines at 2-, 3-, 4- and 6-positions by Suzuki-Miyaura reaction

44. Functionnalization of α-carbolines at the C-6 position

45. Macrobenthos assemblages in Cameroonian mangrove forests: First evidence from the Wouri estuary, Douala

46. Use of ATP analogs to inhibit HIV-1 transcription

47. Targeting low molecular weight cyclin E (LMW-E) in breast cancer

49. 3-Aryl-2-quinolone derivatives: synthesis and characterization of in vitro and in vivo antitumor effects with emphasis on a new therapeutical target connected with cell migration

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