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Research 481–510 of 1000+
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- A case of unilateral congenital triangular alopecia
- Skin Development and Disease: A Molecular Perspective
- Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection?
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Dermoscopy of a Congenital Pigmented Lesion: A Case of Supernumerary Nipple
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Disorders of Keratinization
- Editorial: Retinoids — dermatologists’ drug of the decade
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Alternative uses of dermoscopy in daily clinical practice: An update
- Follicular ichthyosis
- Clinical report of a Holstein's calf with ichthyosis.
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Research Snippets
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Research Snippets
- KRT16 wt Allele