Numerous single gene mutations identified in humans and mice result in nail deformities with many similarities between the species. A spontaneous, autosomal, recessive mutation called witch nails (whnl) is described here where the distal nail matrix and nail bed undergo degenerative changes resulting in formation of an abnormal nail plate causing mice to develop long, curved nails. This mutation arose spontaneously in a colony of MRL/MpJ-Faslpr/J at The Jackson Laboratory. Homozygous mutant mice are recognizable by 8 weeks of age by their long, curved nails. The whnl mutation, mapped on Chromosome 15, is due to a 7-bp insertion identified in the 3\u27 region of exon 9 in the Krt90 gene (formerly Riken cDNA 4732456N10Rik), and is predicted t...
The aim of this thesis is to investigate the effect of genetic mutations on the pathophysiology of t...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...
Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which th...
Numerous single gene mutations identified in humans and mice result in nail deformities with many si...
Inherited and isolated nail malformations are rare and heterogeneous conditions. We identified two c...
In a large-scale ageing study, 30 inbred mouse strains were systematically screened for histologic e...
Nude mice have a mutation in the transcription factor Foxn1nu, resulting in downregulation of hair k...
Nude mice have a mutation in the transcription factor Foxn1(nu), resulting in downregulation of hair...
In a large-scale ageing study, 30 inbred mouse strains were systematically screened for histologic...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
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 ...
Recent studies of mice with hair defects have resulted in major contributions to the understanding o...
Isolated congenital nail dysplasia is an autosomal dominant disorder recently observed in a large fa...
Nails protect the soft tissue of the tips of digits. The molecular mechanism of nail (and claw) deve...
The aim of this thesis is to investigate the effect of genetic mutations on the pathophysiology of t...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...
Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which th...
Numerous single gene mutations identified in humans and mice result in nail deformities with many si...
Inherited and isolated nail malformations are rare and heterogeneous conditions. We identified two c...
In a large-scale ageing study, 30 inbred mouse strains were systematically screened for histologic e...
Nude mice have a mutation in the transcription factor Foxn1nu, resulting in downregulation of hair k...
Nude mice have a mutation in the transcription factor Foxn1(nu), resulting in downregulation of hair...
In a large-scale ageing study, 30 inbred mouse strains were systematically screened for histologic...
Witkop syndrome, also known as tooth and nail syndrome (TNS), is a rare autosomal dominant disorder....
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 ...
Recent studies of mice with hair defects have resulted in major contributions to the understanding o...
Isolated congenital nail dysplasia is an autosomal dominant disorder recently observed in a large fa...
Nails protect the soft tissue of the tips of digits. The molecular mechanism of nail (and claw) deve...
The aim of this thesis is to investigate the effect of genetic mutations on the pathophysiology of t...
<div><p>Pure hair and nail ectodermal dysplasia (PHNED) comprises a heterogeneous group of rare heri...
Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which th...