Shan Yu Fung

Self-assembling peptide as a potential carrier of hydrophobic compounds.

Surface-assisted assembly of an ionic-complementary peptide: controllable growth of nanofibers.

Modification of hydrophilic and hydrophobic surfaces using an ionic-complementary peptide.

Sequence effect of self-assembling peptides on the complexation and in vitro delivery of the hydrophobic anticancer drug ellipticine.

Mechanical-force-induced nucleation and growth of peptide nanofibers at liquid/solid interfaces.

Ionic-complementary peptide-modified highly ordered pyrolytic graphite electrode for biosensor application.

Ionic-complementary peptide matrix for enzyme immobilization and biomolecular sensing.

The potential of nanoscale combinations of self-assembling peptides and amino acids of the Src tyrosine kinase inhibitor in acute lung injury therapy.

Self-assembling peptide-based nanoparticles enhance cellular delivery of the hydrophobic anticancer drug ellipticine through caveolae-dependent endocytosis.

Programming the cellular uptake of physiologically stable peptide-gold nanoparticle hybrids with single amino acids.

Src tyrosine kinase inhibition prevents pulmonary ischemia-reperfusion-induced acute lung injury.

Claudin 1 mediates TNFα-induced gene expression and cell migration in human lung carcinoma cells.

Unbiased screening of marine sponge extracts for anti-inflammatory agents combined with chemical genomics identifies girolline as an inhibitor of protein synthesis.

Combined immunodeficiency associated with homozygous MALT1 mutations.

The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency.

Amino Acid-Dependent Attenuation of Toll-like Receptor Signaling by Peptide-Gold Nanoparticle Hybrids.

The paracaspase MALT1 cleaves HOIL1 reducing linear ubiquitination by LUBAC to dampen lymphocyte NF-κB signalling.

Successful clinical treatment and functional immunological normalization of human MALT1 deficiency following hematopoietic stem cell transplantation.

Formulation of hydrophobic therapeutics with self-assembling peptide and amino acid: A new platform for intravenous drug delivery.

Endosomal pH modulation by peptide-gold nanoparticle hybrids enables potent anti-inflammatory activity in phagocytic immune cells.