Results 231 to 240 of about 42,234 (281)
Combinatorial Probabilities of Multiple Fragmentation Events Explain Polypeptide MS/MS Intensity Distribution, Overrepresentation of Smaller Fragments, and Missing Middle of Top-Down MS. [PDF]
Yang W, Alam N, Agar JN.
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This study explores the feasibility of expressing the antitumoral protein Amblyomin‐X through a suicide gene therapy approach and investigates its intracellular fate after gene delivery. Although the gene is efficiently expressed, melanoma cells rapidly degrade the Amblyomin‐X protein via proteasome activity.
Victor Dal Posolo Cinel +4 more
wiley +1 more source
Lignonaut: designing diverse combinatorial libraries for the exploration and annotation of lignin oligomer spaces. [PDF]
Norberg M, Sandahl M, Spégel P.
europepmc +1 more source
Mapping the Substrate Specificity Landscape of PAD2 and PAD4 Enzymes. [PDF]
Borbély A +6 more
europepmc +1 more source
Stringent selection on kinetics of condensation reactions: early steps in chemical evolution.
Capera-Aragones P +6 more
europepmc +1 more source
Dynamic Combinatorial Chemistry [PDF]
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Peter T Corbett +2 more
exaly +4 more sources
Dynamic combinatorial chemistry
A combinatorial library that responds to its target by increasing the concentration of strong binders at the expense of weak binders sounds ideal. Dynamic combinatorial chemistry has the potential to achieve exactly this. In this review, we will highlight the unique features that distinguish dynamic combinatorial chemistry from traditional ...
Sijbren, Otto +2 more
openaire +3 more sources
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Combinatorial chemistry of hydantoins
Bioorganic & Medicinal Chemistry Letters, 1998Access to combinatorial chemistry of hydantoins is provided by convenient and versatile methods for the solid phase synthesis of libraries of 3,5-, 1,3- and 1,3,5-substituted hydantoins. The preparation of trisubstituted hydantoins features a Mitsunobu reaction for introduction of the substituent on N-1.
Boeijen, A. +2 more
openaire +3 more sources

