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A mostrar 1 - 20 resultados de 664 para a pesquisa '((((eur j) OR (mur j))) OR (eun j)) ((((med cem) OR (led em))) OR (med chem))*', זמן שאילתה: 1.01seg Refinar resultados
Editorial – IChemE Special Issue on Climate Change
The role of smoking in the development and progression of structural damage in axial SpA patients: A systematic review and meta-analysis

Structure Activity Relationships of 1,4-Dihydropyridines That Act as Enhancers of the Vanilloid Receptor 1 (TRPV1)
Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries

Simultaneous determination of methylcarbamate and ethylcarbamate in fermented foods and beverages by derivatization and GC-MS analysis
CRISPR/dCas9-mediated biosensor for detection of tick-borne diseases

Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4
Effect of cinnamamides on atopic dermatitis through regulation of IL-4 in CD4(+) cells

Evaluation of caffeine as inhibitor against collagenase, elastase and tyrosinase using in silico and in vitro approach
Synthesis and antioxidant properties of dendritic polyphenols

(S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5
Non-proteinogenic amino acids in the pThr-2 position of a pentamer peptide that confer high binding affinity for the polo box domain (PBD) of polo-like kinase 1 (Plk1)

Corrigendum to “Synthesis and cytotoxic activity of novel Aring cleaved ursolic acid derivatives in human nonsmall cell lung cancer cells” [Eur. J. Med. Chem. 123 (2016) 317–331]
Development of Novel Epoxyketone-Based Proteasome Inhibitors as a Strategy To Overcome Cancer Resistance to Carfilzomib and Bortezomib

Effects on Polo-like Kinase 1 Polo-box Domain Binding Affinities of Peptides Incurred by Structural Variation at the Phosphoamino Acid Position
Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles

Elucidation of New Binding Interactions with the Human Tsg101 Protein Using Modified HIV-1 Gag-p6 Derived Peptide Ligands
A POTENT AND SELECTIVE INHIBITOR TARGETING HUMAN AND MURINE 12/15-LOX

Optimizing Thiadiazole Analogues of Resveratrol vs. Three Chemopreventive Targets
A novel nucleic acid amplification system based on nano-gap embedded active disk resonators

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