Loss of functional hairless (HR) transcriptional repressor leads to utricle formation and congenital hair loss both in mice and men. Studies in mice have shown that this is preceded by overexpression of caspase-14 at the infundibulum in the hair follicle before conversion to utricle occurs. In this report, we show that HR regulates caspase-14 expression dependent on its interaction with histone deacetylases, implicating chromatin remodelling in the transcriptional regulation of caspase-14. However, crossing hairless mutant mice with caspase-14-deficient mice revealed that caspase-14 overexpression is not the cause of utricle formation
Mutation of the hairless (hr) gene in mice causes severe abnormalities during the first hair follicl...
It is increasingly evident that the molecular mechanisms underlying hair follicle differentiation an...
Many biochemical pathways involved in hair and skin development have not been investigated. Here, we...
Loss of functional hairless (HR) transcriptional repressor leads to utricle formation and congenital...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
Mice that carry a mutation at the hairless (hr) locus develop seemingly normal hair follicles (HF) b...
Hair follicles are unique organs undergoing regular cycles of proliferation, differentiation, and ap...
Hair follicles are unique organs undergoing regular cycles of proliferation, differentiation, and ap...
Caspase-14 is a unique member of the evolutionarily conserved family of cysteinyl aspartate-specific...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Mutation of the hairless (hr) gene in mice causes severe abnormalities during the first hair follicl...
It is increasingly evident that the molecular mechanisms underlying hair follicle differentiation an...
Many biochemical pathways involved in hair and skin development have not been investigated. Here, we...
Loss of functional hairless (HR) transcriptional repressor leads to utricle formation and congenital...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
International audienceThe hairless gene in mammals encodes a nuclear factor that is highly expressed...
Mice that carry a mutation at the hairless (hr) locus develop seemingly normal hair follicles (HF) b...
Hair follicles are unique organs undergoing regular cycles of proliferation, differentiation, and ap...
Hair follicles are unique organs undergoing regular cycles of proliferation, differentiation, and ap...
Caspase-14 is a unique member of the evolutionarily conserved family of cysteinyl aspartate-specific...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Caspase-14 is a recent addition to the caspase family of aspartate proteases involved in apoptotic p...
Mutation of the hairless (hr) gene in mice causes severe abnormalities during the first hair follicl...
It is increasingly evident that the molecular mechanisms underlying hair follicle differentiation an...
Many biochemical pathways involved in hair and skin development have not been investigated. Here, we...