The hard-keratin-containing portion of the murine hair shaft displays a positive immunoreactivity with an antibody against the soft epithelial keratin, K17. The K17-expressing cell population is located in the medulla compartment of the hair. Consistent with this observation, K17-containing cells also occur in the presumptive medulla precursor cells located in the hair follicle matrix. Western blot analysis of hair extracts prepared from a number of mouse strains confirms this observation and suggests that K17 expression in the hair shaft is a general trait in this species. The expression of K17 in human hair extracts is restricted to eyebrow and facial hair samples. These are the major sites for the occurrence of the pili torti (twisted ha...
Although it has been shown previously that an acidic (type I) “soft” keratin can interact with many ...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...
Inactivating the type I keratin 17 gene (mK17) causes severe but reversible hair loss in a strain-de...
KRT75 (formerly known as K6hf) is one of the isoforms of the keratin 6 (KRT6) family located within ...
KRT75 (formerly known as K6hf) is one of the isoforms of the keratin 6 (KRT6) family located within ...
Type I and type II keratins form the heteropolymeric intermediate filament cytoskeleton, which is th...
Pachyonychia congenita (PC) is a group of autosomal dominant disorders characterized by dystrophic n...
More than half of the known keratin genes (n≈50) are expressed in the hair follicle. An in-depth kno...
Keratin 17 (K17) expression is currently considered to be associated with hyperplastic or malignant ...
Pachyonychia congenita type 2 is an inherited ectodermal dysplasia characterized by hypertrophic nai...
Pachyonychia congenita type 2 is an inherited ectodermal dysplasia characterized by hypertrophic nai...
Pachyonychia congenita type 2 (PC-2; Jackson-Lawler syndrome) is an autosomal dominant disorder char...
Pachyonychia congenita (PC) is a rare autosomal dominant condition characterized by multiple ectoder...
Keratins are the intermediate filament proteins specifically expressed by epithelial cells. The Huma...
Although it has been shown previously that an acidic (type I) “soft” keratin can interact with many ...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...
Inactivating the type I keratin 17 gene (mK17) causes severe but reversible hair loss in a strain-de...
KRT75 (formerly known as K6hf) is one of the isoforms of the keratin 6 (KRT6) family located within ...
KRT75 (formerly known as K6hf) is one of the isoforms of the keratin 6 (KRT6) family located within ...
Type I and type II keratins form the heteropolymeric intermediate filament cytoskeleton, which is th...
Pachyonychia congenita (PC) is a group of autosomal dominant disorders characterized by dystrophic n...
More than half of the known keratin genes (n≈50) are expressed in the hair follicle. An in-depth kno...
Keratin 17 (K17) expression is currently considered to be associated with hyperplastic or malignant ...
Pachyonychia congenita type 2 is an inherited ectodermal dysplasia characterized by hypertrophic nai...
Pachyonychia congenita type 2 is an inherited ectodermal dysplasia characterized by hypertrophic nai...
Pachyonychia congenita type 2 (PC-2; Jackson-Lawler syndrome) is an autosomal dominant disorder char...
Pachyonychia congenita (PC) is a rare autosomal dominant condition characterized by multiple ectoder...
Keratins are the intermediate filament proteins specifically expressed by epithelial cells. The Huma...
Although it has been shown previously that an acidic (type I) “soft” keratin can interact with many ...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main...