Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic palmoplantar keratoderma (FNEPPK). By generating keratin 16 (Krt16)–deficient mice, Lessard and Coulombe, as described in this issue, have generated a mouse model to replicate these palmoplantar lesions. Studies using this model may provide novel insights into the molecular mechanisms responsible for the formation of palmoplantar lesions in PC and FNEPPK patients
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/154394/1/bjd18033.pdfhttps://deepblue....
Pachyonychia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations...
Mutations in SLURP1 cause mal de Meleda, a rare palmoplantar keratoderma (PPK). SLURP1 is a secreted...
Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic pa...
The similarities between the human and mouse genomes often allow researchers to make accurate predic...
Keratin 16 (KRT16 in human, Krt16 in mouse), a type I intermediate filament protein, is constitutive...
Molecular characterization and assessment of therapeutic outcomes for inherited cutaneous disorders ...
Palmoplantar keratodermas (PPK) are a group of rare skin disorders characterized by abnormal thicken...
Pachyonychia congenita type 1 (PC-1) is an autosomal dominant ectodermal dysplasia characterized by ...
The type I intermediate filament keratin 16 (K16) is constitutively expressed in ectoderm‐derived ap...
This thesis presents novel insight into the pathophysiology of palmoplantar keratoderma and previous...
Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided in...
The palmoplantar keratodermas (PPKs) are a large group of clinically and genetically heterogeneous g...
Keratin 9 (KRT9/Krt9) is a type I intermediate filament protein that is constitutively expressed in ...
The palmoplantar keratodermas (PPKs) are a large group of clinically and genetically heterogeneous g...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/154394/1/bjd18033.pdfhttps://deepblue....
Pachyonychia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations...
Mutations in SLURP1 cause mal de Meleda, a rare palmoplantar keratoderma (PPK). SLURP1 is a secreted...
Palmoplantar keratoderma is a hallmark of pachyonychia congenita (PC) and focal non-epidermolytic pa...
The similarities between the human and mouse genomes often allow researchers to make accurate predic...
Keratin 16 (KRT16 in human, Krt16 in mouse), a type I intermediate filament protein, is constitutive...
Molecular characterization and assessment of therapeutic outcomes for inherited cutaneous disorders ...
Palmoplantar keratodermas (PPK) are a group of rare skin disorders characterized by abnormal thicken...
Pachyonychia congenita type 1 (PC-1) is an autosomal dominant ectodermal dysplasia characterized by ...
The type I intermediate filament keratin 16 (K16) is constitutively expressed in ectoderm‐derived ap...
This thesis presents novel insight into the pathophysiology of palmoplantar keratoderma and previous...
Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided in...
The palmoplantar keratodermas (PPKs) are a large group of clinically and genetically heterogeneous g...
Keratin 9 (KRT9/Krt9) is a type I intermediate filament protein that is constitutively expressed in ...
The palmoplantar keratodermas (PPKs) are a large group of clinically and genetically heterogeneous g...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/154394/1/bjd18033.pdfhttps://deepblue....
Pachyonychia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations...
Mutations in SLURP1 cause mal de Meleda, a rare palmoplantar keratoderma (PPK). SLURP1 is a secreted...