Activation of heparanase by ultraviolet B irradiation leads to functional loss of basement membrane at the dermal–epidermal junction in human skin

Differential binding of fibroblast growth factor-2 and -7 to basement membrane heparan sulfate: comparison of normal and abnormal human tissues.

Characterization of growth factor-binding structures in heparin/heparan sulfate using an octasaccharide library.

Specificities of heparan sulphate proteoglycans in developmental processes.

Heparanase activation induces epidermal hyperplasia, angiogenesis, lymphangiogenesis and wrinkles.

Cathepsin L is responsible for processing and activation of proheparanase through multiple cleavages of a linker segment.

Heparanase 1: a key participant of inner root sheath differentiation program and hair follicle homeostasis.

Heparanase stimulation of protease expression implicates it as a master regulator of the aggressive tumor phenotype in myeloma.

Matrix metalloproteinase-9 associated with heparan sulphate chains of GPI-anchored cell surface proteoglycans mediates motility of murine colon adenocarcinoma cells.

Anti-heparanase monoclonal antibody enhances heparanase enzymatic activity and facilitates wound healing.

Distinct architecture of lymphatic vessels induced by chimeric vascular endothelial growth factor-C/vascular endothelial growth factor heparin-binding domain fusion proteins.

Activation of heparanase by ultraviolet B irradiation leads to functional loss of basement membrane at the dermal–epidermal junction in human skin

Characterization and mechanisms of photoageing-related changes in skin. Damages of basement membrane and dermal structures.

Expression of heparanase in basal cell carcinoma and squamous cell carcinoma*

Heparanase Inhibitors Facilitate the Assembly of the Basement Membrane in Artificial Skin

Acute UV Irradiation Increases Heparan Sulfate Proteoglycan Levels in Human Skin

Ultraviolet-B irradiation induces epidermal up-regulation of heparanase expression and activity.

Significance of Heparanase in Cancer and Inflammation

Differential binding of fibroblast growth factor-2 and -7 to basement membrane heparan sulfate: comparison of normal and abnormal human tissues.

Characterization of growth factor-binding structures in heparin/heparan sulfate using an octasaccharide library.

Specificities of heparan sulphate proteoglycans in developmental processes.

Heparanase activation induces epidermal hyperplasia, angiogenesis, lymphangiogenesis and wrinkles.

Cathepsin L is responsible for processing and activation of proheparanase through multiple cleavages of a linker segment.

Heparanase 1: a key participant of inner root sheath differentiation program and hair follicle homeostasis.

Heparanase stimulation of protease expression implicates it as a master regulator of the aggressive tumor phenotype in myeloma.

Matrix metalloproteinase-9 associated with heparan sulphate chains of GPI-anchored cell surface proteoglycans mediates motility of murine colon adenocarcinoma cells.

Anti-heparanase monoclonal antibody enhances heparanase enzymatic activity and facilitates wound healing.

Distinct architecture of lymphatic vessels induced by chimeric vascular endothelial growth factor-C/vascular endothelial growth factor heparin-binding domain fusion proteins.

Activation of heparanase by ultraviolet B irradiation leads to functional loss of basement membrane at the dermal–epidermal junction in human skin

Characterization and mechanisms of photoageing-related changes in skin. Damages of basement membrane and dermal structures.

Expression of heparanase in basal cell carcinoma and squamous cell carcinoma*

Heparanase Inhibitors Facilitate the Assembly of the Basement Membrane in Artificial Skin

Acute UV Irradiation Increases Heparan Sulfate Proteoglycan Levels in Human Skin

Ultraviolet-B irradiation induces epidermal up-regulation of heparanase expression and activity.

Significance of Heparanase in Cancer and Inflammation

Differential binding of fibroblast growth factor-2 and -7 to basement membrane heparan sulfate: comparison of normal and abnormal human tissues.

Characterization of growth factor-binding structures in heparin/heparan sulfate using an octasaccharide library.

Specificities of heparan sulphate proteoglycans in developmental processes.

Heparanase activation induces epidermal hyperplasia, angiogenesis, lymphangiogenesis and wrinkles.

Cathepsin L is responsible for processing and activation of proheparanase through multiple cleavages of a linker segment.

Heparanase 1: a key participant of inner root sheath differentiation program and hair follicle homeostasis.

Heparanase stimulation of protease expression implicates it as a master regulator of the aggressive tumor phenotype in myeloma.

Matrix metalloproteinase-9 associated with heparan sulphate chains of GPI-anchored cell surface proteoglycans mediates motility of murine colon adenocarcinoma cells.

Anti-heparanase monoclonal antibody enhances heparanase enzymatic activity and facilitates wound healing.

Distinct architecture of lymphatic vessels induced by chimeric vascular endothelial growth factor-C/vascular endothelial growth factor heparin-binding domain fusion proteins.