Generalized junctional epidermolysis bullosa (JEB) is caused by mutations in LAMA3,LAMB3,or LAMC2,which together encode laminin-332, a hetero-trimeric protein consisting ofa3,b3, andg2chain. In nonlethal generalized intermediate JEB, laminin-332 is highly reduced, and hemidesmosomes are rudimentary or completely absent, leading to blister formation within the lamina lucida of the basement membrane upon minor trauma. The resulting chronic skin wounds invariably develop recurrent infections and scarring, which greatly impair patients\u2019 quality of life. We report on a patient in whom gene-corrected epidermal sheets were transplanted onto a large nonhealing epidermal ulceration following a good manufacturing practice protoco
Deficiency of the basement membrane component laminin-5 (LAM5) causes junctional epidermolysis bullo...
Laminin 332-deficient junctional epidermolysis bullosa (JEB) is a severe genetic skin disease. JEB i...
Epidermolysis bullosa (EB) is an inherited skin disease. Patients have lifelong fragile skin leading...
Generalized junctional epidermolysis bullosa (JEB) is caused by mutations in LAMA3,LAMB3,or LAMC2...
International audienceThe continuous renewal of human epidermis is sustained by stem cells contained...
Junctional epidermolysis bullosa (JEB) is a group of severe, inherited skin diseases caused by mutat...
SummaryWe report a long-term follow-up (6.5 years) of a phase I/II clinical trial envisaging the use...
We report a long-term follow-up (6.5 years) of a phase I/II clinical trial envisaging the use of aut...
Keratinocytes and dermal fibroblasts express adhesive proteins that ensure the epidermis remains att...
Herlitz junctional epidermolysis bullosa (H-JEB) provides a promising model for somatic gene therapy...
Epidermolysis bullosa (EB) is a group of devastating genetic diseases characterized by skin and muco...
Deficiency of basement membrane heterotrimeric laminin 332 component, coded by LAMA3, LAMB3, and LAM...
Background: Epidermolysis bullosa (EB) is a group of genetic blistering diseases. Despite many effor...
Junctional epidermolysis bullosa (JEB) is a hereditary blistering disease caused by reduced dermal-e...
Background: Epidermolysis bullosa (EB) is a genetic, heterogeneous, trauma-induced blistering diseas...
Deficiency of the basement membrane component laminin-5 (LAM5) causes junctional epidermolysis bullo...
Laminin 332-deficient junctional epidermolysis bullosa (JEB) is a severe genetic skin disease. JEB i...
Epidermolysis bullosa (EB) is an inherited skin disease. Patients have lifelong fragile skin leading...
Generalized junctional epidermolysis bullosa (JEB) is caused by mutations in LAMA3,LAMB3,or LAMC2...
International audienceThe continuous renewal of human epidermis is sustained by stem cells contained...
Junctional epidermolysis bullosa (JEB) is a group of severe, inherited skin diseases caused by mutat...
SummaryWe report a long-term follow-up (6.5 years) of a phase I/II clinical trial envisaging the use...
We report a long-term follow-up (6.5 years) of a phase I/II clinical trial envisaging the use of aut...
Keratinocytes and dermal fibroblasts express adhesive proteins that ensure the epidermis remains att...
Herlitz junctional epidermolysis bullosa (H-JEB) provides a promising model for somatic gene therapy...
Epidermolysis bullosa (EB) is a group of devastating genetic diseases characterized by skin and muco...
Deficiency of basement membrane heterotrimeric laminin 332 component, coded by LAMA3, LAMB3, and LAM...
Background: Epidermolysis bullosa (EB) is a group of genetic blistering diseases. Despite many effor...
Junctional epidermolysis bullosa (JEB) is a hereditary blistering disease caused by reduced dermal-e...
Background: Epidermolysis bullosa (EB) is a genetic, heterogeneous, trauma-induced blistering diseas...
Deficiency of the basement membrane component laminin-5 (LAM5) causes junctional epidermolysis bullo...
Laminin 332-deficient junctional epidermolysis bullosa (JEB) is a severe genetic skin disease. JEB i...
Epidermolysis bullosa (EB) is an inherited skin disease. Patients have lifelong fragile skin leading...