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Research 481–510 of 1000+
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- The investigation of insulin resistance and metabolic syndrome in male patients with early-onset androgenetic alopecia
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- GATA3 inhibits proliferation and induces expression of both early and late differentiation markers in keratinocytes of the human epidermis
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Hair That Is Difficult to Manage in a Hispanic Girl
- IL-15 in alopecia areata: the immune tolerance mechanistic insights and translational perspectives
- The molecular pathogenesis of Trichilemmal carcinoma
- Retinoids in Dermatology
- Non-surgical Modalities of Facial Rejuvenation and Aesthetics
- Extensive Spiculated Follicular Porokeratosis With Alopecia: A Case Report
- Analysis of Isotretinoin-Induced Alterations in the Levels of Plasma Trace Elements: Investigation of the Relationship Between Magnesium, Phosphorus, Potassium, Zinc, and Treatment-Related Side Effects
- Distribution and number of epidermal growth factor receptors in skin is related to epithelial cell growth
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Hox in hair growth and development
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Comparative Anatomy of Mouse and Human Nail Units
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- CD80 on skin stem cells promotes local expansion of regulatory T cells upon injury to orchestrate repair within an inflammatory environment
- Iron: a cosmetic constituent but an essential nutrient for healthy skin
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hidradenitis suppurativa: A folliculotropic disease of innate immune barrier dysfunction?