Any rational therapy benefits from an understanding of basic biology and the simplicity of its strategy. Among keratinopathies, epidermolytic palmoplantar keratoderma stands out by virtue of hotspot mutations in the KRT9 gene, exclusively expressed in the palmoplantar epidermis. In this issue, Leslie Pedrioli et al. report on the successful application of KRT9-specific siRNAs in cultured cells and in a mouse model. The study beautifully illustrates the potency of a thorough experimental approach and the challenges that remain, especially in its delivery
RNA interference offers a novel approach for developing therapeutics for dominant-negative genetic d...
Epidermolysis bullosa simplex (EBS) is an incurable, inherited skin-blistering disorder predominantl...
Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic pa...
Any rational therapy benefits from an understanding of basic biology and the simplicity of its strat...
Keratin 9 (K9) is a type I intermediate filament protein whose expression is confined to the supraba...
Epidermolytic palmoplantar keratoderma (EPPK) is one of >30 autosomal-dominant human keratinizing di...
CRISPR/Cas9 has been confirmed as a distinctly efficient, simple-to-configure, highly specific genom...
This thesis presents novel insight into the pathophysiology of palmoplantar keratoderma and previous...
Epidermolytic palmoplantar keratoderma (EPPK) is one of >30 autosomal-dominant human keratinizing...
Epidermolytic palmoplantar keratoderma (EPPK, OMIM 144200) is an autosomal dominant inherited diseas...
Pachyonychia congenita (PC) is an autosomal-dominant keratin disorder where the most painful, debili...
Dominant mutations that interfere with the assembly of keratin filaments cause painful and disfiguri...
The term ‘keratin ’ is generally accepted to refer to the epithelial keratins of soft and hard epith...
Epidermolytic palmoplantar keratodenna is an autosomal dominant skin disorder characterized by hyper...
Keratoderma – pathological hyperkeratosis of palms and soles - is a cause of disability in many cli...
RNA interference offers a novel approach for developing therapeutics for dominant-negative genetic d...
Epidermolysis bullosa simplex (EBS) is an incurable, inherited skin-blistering disorder predominantl...
Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic pa...
Any rational therapy benefits from an understanding of basic biology and the simplicity of its strat...
Keratin 9 (K9) is a type I intermediate filament protein whose expression is confined to the supraba...
Epidermolytic palmoplantar keratoderma (EPPK) is one of >30 autosomal-dominant human keratinizing di...
CRISPR/Cas9 has been confirmed as a distinctly efficient, simple-to-configure, highly specific genom...
This thesis presents novel insight into the pathophysiology of palmoplantar keratoderma and previous...
Epidermolytic palmoplantar keratoderma (EPPK) is one of >30 autosomal-dominant human keratinizing...
Epidermolytic palmoplantar keratoderma (EPPK, OMIM 144200) is an autosomal dominant inherited diseas...
Pachyonychia congenita (PC) is an autosomal-dominant keratin disorder where the most painful, debili...
Dominant mutations that interfere with the assembly of keratin filaments cause painful and disfiguri...
The term ‘keratin ’ is generally accepted to refer to the epithelial keratins of soft and hard epith...
Epidermolytic palmoplantar keratodenna is an autosomal dominant skin disorder characterized by hyper...
Keratoderma – pathological hyperkeratosis of palms and soles - is a cause of disability in many cli...
RNA interference offers a novel approach for developing therapeutics for dominant-negative genetic d...
Epidermolysis bullosa simplex (EBS) is an incurable, inherited skin-blistering disorder predominantl...
Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic pa...