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Research 481–510 of 830
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Keratins and skin disease
- Vitamin D and the Skin: A Review for Dermatologists
- Off-label uses of retinoids in dermatology
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Animals in Dermatology
- Hydrobiome of Thermal Waters: Potential Use in Dermocosmetics
- 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
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- From Axioms to New Insights into Dandruff
- 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
- Thyroid hormone action on skin
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Keratosis follicularis spinulosa decalvans in a family
- 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