Publicaciones en colaboración con investigadores/as de University of Bristol (14)

2023

  1. Multicolor Photoluminescent Carbon Dots à La Carte for Biomedical Applications

    ACS Applied Materials and Interfaces, Vol. 15, Núm. 38, pp. 44711-44721

  2. Reverse thiophosphorylase activity of a glycoside phosphorylase in the synthesis of an unnatural Manβ1,4GlcNAc library

    Chemical Science, Vol. 14, Núm. 42, pp. 11638-11646

2022

  1. Carbon dot-based fluorescent antibody nanoprobes as brain tumour glioblastoma diagnostics

    Nanoscale Advances, Vol. 4, Núm. 7, pp. 1770-1778

  2. Carbon-based glyco-nanoplatforms: towards the next generation of glycan-based multivalent probes

    Chemical Society Reviews, Vol. 51, Núm. 24, pp. 9960-9985

  3. Recent Advances on Multivalent Carbon Nanoform-Based Glycoconjugates

    Current Medicinal Chemistry, Vol. 29, Núm. 7, pp. 1232-1257

  4. Recent applications of ionic liquid-based tags in glycoscience

    Carbohydrate Research, Vol. 520

  5. Reengineering of cancer cell surface charges can modulate cell migration

    Chemical Communications, Vol. 58, Núm. 36, pp. 5522-5525

  6. Synthesis of Chiral Ionic Liquids from Natural Monosaccharides

    European Journal of Organic Chemistry, Vol. 2022, Núm. 21

2021

  1. Benefits of Chemical Sugar Modifications Introduced by Click Chemistry for Glycoproteomic Analyses

    Journal of the American Society for Mass Spectrometry, Vol. 32, Núm. 9, pp. 2366-2375

  2. Carbon dots as an emergent class of antimicrobial agents

    Nanomaterials, Vol. 11, Núm. 8

  3. Glioma Stem-Like Cells and Metabolism: Potential for Novel Therapeutic Strategies

    Frontiers in Oncology, Vol. 11

  4. Imidazolium labelling permits the sensitive mass-spectrometric detection ofN-glycosides directly from serum

    Chemical Communications, Vol. 57, Núm. 57, pp. 7003-7006

2020

  1. Chemo-selective Rh-catalysed hydrogenation of azides into amines

    Carbohydrate Research, Vol. 489

2011

  1. Molecular Recognition of beta-O-GlcNAc Glycopeptides by a Lectin-Like Receptor: Binding Modulation by the Underlying Ser or Thr Amino Acids

    Chembiochem : a European journal of chemical biology, Vol. 12, Núm. 1, pp. 110-117