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「"Overkleeft HS"[Author]」の検索結果

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Reagent Controlled Glycosylations for the Assembly of Well-defined Pel Oligosaccharides.

Synthesis and Structural Analysis of Aspergillus fumigatus Galactosaminogalactans featuring α-galactose, α-galactosamine and α-N-acetyl galactosamine linkages.

Plant Glycosides and Glycosidases: A Treasure-Trove for Therapeutics.

Olaparib-Based Photoaffinity Probes for PARP-1 Detection in Living Cells.

Immunoproteasome inhibitor-doxorubicin conjugates target Multiple Myeloma cells and release Doxorubicin upon low-dose photon irradiation.

Skin barrier lipid enzyme activity in Netherton patients is associated with protease activity and ceramide abnormalities.

Synthesis of orthogonally protected and functionalized bacillosamines.

Fluorogenic Bifunctional Trans-cyclooctenes as Efficient Tools for Investigating Click-to-Release Kinetics.

Reagent controlled stereoselective synthesis of teichoic acid α-(1,2)-glucans.

Skin of atopic dermatitis patients shows disturbed β-glucocerebrosidase and acid sphingomyelinase activity that relates to changes in stratum corneum lipid composition.

Rational Design of Mechanism-Based Inhibitors and Activity-Based Probes for the Identification of Retaining α-L-Arabinofuranosidases.

-mannosyl lysine for solid phase assembly of mannosylated peptide conjugate cancer vaccines.

STA-55, An Easily Accessible Broadspectrum Activity-Based Aldehyde Dehydrogenase Probe.

Development of a Retinal-Based Probe for the Profiling of Retinaldehyde Dehydrogenases in Cancer Cells.

Identification of α,β-Hydrolase Domain Containing Protein 6 as a Diacylglycerol Lipase in Neuro-2a Cells.

Direct Stereoselective Aziridination of Cyclohexenols with 3-Amino-2-(trifluoromethyl)quinazolin-4(3)-one in the Synthesis of Cyclitol Aziridine Glycosidase Inhibitors.

Glycosphingolipids and lysosomal storage disorders as illustrated by gaucher disease.

Discovering the Microbial Enzymes Driving Drug Toxicity with Activity-Based Protein Profiling.

Trypanosoma brucei: inhibition of cathepsin L is sufficient to kill bloodstream forms.

ABHD2 Inhibitor Identified by Activity-Based Protein Profiling Reduces Acrosome Reaction.

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