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Research 91–120 of 1000+
- Ichthyosis hystrix
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Cylindroma as Tumor of Hair Follicle Origin
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Spreading of Isolated Ptch Mutant Basal Cell Carcinoma Precursors Is Physiologically Suppressed and Counteracts Tumor Formation in Mice
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Genetic Susceptibility to Alopecia
- Morphological Approach to Hair Disorders
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Loose anagen syndrome in one identical twin girl.
- Congenital atrichia with papular lesions
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder