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Research 451–480 of 1000+
- Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Extracellular vesicles from adipose-derived stem cells ameliorate ultraviolet B-induced skin photoaging by attenuating reactive oxygen species production and inflammation
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Molecular signaling in feather morphogenesis
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Scarless wound healing: Transitioning from fetal research to regenerative healing
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Exploring Acne Treatments: From Pathophysiological Mechanisms to Emerging Therapies
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Lineage Analysis of Epidermal Stem Cells
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling