The paper in this issue by Has and co-workers reports 15 non-Herlitz epidermolysis bullosa patients with the same single amino-acid substitution in collagen XVII, all of whom presented with clinical and pathological features resembling Kindler syndrome. Here we consider why and how a hemidesmosomal pathology can mimic a focal adhesion bond disease, both clinically and ultrastructurally
The hemidesmosome (HD)-anchoring filament complex comprises a multiprotein complex that aids the att...
Epidermolysis bullosa (EB) is caused by mutations in as many as 19 distinct genes. We have developed...
The hemidesmosome is a specialized transmembrane complex that mediates the binding of epithelial cel...
The paper in this issue by Has and co-workers reports 15 non-Herlitz epidermolysis bullosa patients ...
BP180/collagen XVII is a hemidesmosomal transmembrane molecule serving as cell-surface receptor. Mut...
In 1990 the role of basement membranes in human disease was established by the identification of COL...
Hemidesmosomes are complex, multiprotein structures that mediate the attachment of epithelial cells ...
Kindler syndrome is an autosomal recessive disorder characterized by skin atrophy and blistering. It...
Bullous pemphigoid antigen 2 (BP180; COL17A1) collagen gene mutations typically result in nonlethal ...
In skin, basal keratinocytes in the epidermis are tightly attached to the underlying dermis by the b...
Junctional epidermolysis bullosis QEB) is a heterogeneous inherited blistering disorder of human epi...
Integrin α6β4 is a hemidesmosomal transmembrane molecule involved in maintaining basal cell-matrix a...
Junctional epidermolysis bullosa is a group of hereditary bullous disorders resulting from defects i...
Junctional epidermolysis bullosa (JEB) comprises a group of inherited autosomal recessive blistering...
The candidate gene approach in tracking the underlying cause of a number of genetic skin disorders h...
The hemidesmosome (HD)-anchoring filament complex comprises a multiprotein complex that aids the att...
Epidermolysis bullosa (EB) is caused by mutations in as many as 19 distinct genes. We have developed...
The hemidesmosome is a specialized transmembrane complex that mediates the binding of epithelial cel...
The paper in this issue by Has and co-workers reports 15 non-Herlitz epidermolysis bullosa patients ...
BP180/collagen XVII is a hemidesmosomal transmembrane molecule serving as cell-surface receptor. Mut...
In 1990 the role of basement membranes in human disease was established by the identification of COL...
Hemidesmosomes are complex, multiprotein structures that mediate the attachment of epithelial cells ...
Kindler syndrome is an autosomal recessive disorder characterized by skin atrophy and blistering. It...
Bullous pemphigoid antigen 2 (BP180; COL17A1) collagen gene mutations typically result in nonlethal ...
In skin, basal keratinocytes in the epidermis are tightly attached to the underlying dermis by the b...
Junctional epidermolysis bullosis QEB) is a heterogeneous inherited blistering disorder of human epi...
Integrin α6β4 is a hemidesmosomal transmembrane molecule involved in maintaining basal cell-matrix a...
Junctional epidermolysis bullosa is a group of hereditary bullous disorders resulting from defects i...
Junctional epidermolysis bullosa (JEB) comprises a group of inherited autosomal recessive blistering...
The candidate gene approach in tracking the underlying cause of a number of genetic skin disorders h...
The hemidesmosome (HD)-anchoring filament complex comprises a multiprotein complex that aids the att...
Epidermolysis bullosa (EB) is caused by mutations in as many as 19 distinct genes. We have developed...
The hemidesmosome is a specialized transmembrane complex that mediates the binding of epithelial cel...