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Research 31–60 of 1000+
- Congenital hair loss disorders: Rare, but not too rare
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Molecular Genetics of Alopecias
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Keratin disorders: from gene to therapy
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Genetically separable determinants of hair keratin gene expression
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Histologic morphology and involucrin, filaggrin, and keratin expression in normal canine skin from dogs of different breeds and coat types
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation