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Research 511–540 of 810
- Commentary: Darier-White Disease
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Clinical Snippets
- [Acitretine].
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Cell death in the skin
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- The molecular basis of human keratin disorders
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Keratins and skin disease
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Dissecting cellulitis (Perifolliculitis Capitis Abscedens et Suffodiens): a comprehensive review focusing on new treatments and findings of the last decade with commentary comparing the therapies and causes of dissecting cellulitis to hidradenitis suppura
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Enzymology of the hair follicle.
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- Ulerythema ophryogenes with multiple congenital anomalies
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Nilotinib-Induced Keratosis Pilaris
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction