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Research 151–180 of 1000+
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Signal integrator function of CXXC5 in Cancer
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- Melanocytes in regenerative medicine applications and disease modeling
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- The great atopic diseases epidemic: does chemical exposure play a role?
- Abstracts
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- 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
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Recombinant human hepatitis B vaccine initiating alopecia areata: testing the hypothesis using the C3H/HeJ mouse model
- Third International Research Workshop on Alopecia Areata
- Factors associated with early-onset androgenetic alopecia: A scoping review
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease