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Research 301–330 of 1000+
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Regenerative Medicine of Epidermal Structures
- A preview of selected articles
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Molecular basis of androgen insensitivity
- Evaluation of Polyacrylonitrile Nonwoven Mats and Silver–Gold Bimetallic Nanoparticle-Decorated Nonwoven Mats for Potential Promotion of Wound Healing In Vitro and In Vivo and Bone Growth In Vitro
- An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Neural Wiskott-Aldrich syndrome protein modulates Wnt signaling and is required for hair follicle cycling in mice
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Endoplasmic reticulum stress at the crossroads of progeria and atherosclerosis
- Characterization of tiger tail banding and hair shaft abnormalities in trichothiodystrophy
- Prevalence of Cobalt in the Environment and Its Role in Biological Processes
- The Mitochondrial Blueprint of Skin Aging: From Damage Signals to Dermatologic Interventions
- 1433 Role of BNC1 in keratinocytes proliferation and migration: A critical regulator of wound healing?
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- In this Issue
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- C/EBPα and C/EBPβ Are Required for Sebocyte Differentiation and Stratified Squamous Differentiation in Adult Mouse Skin
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Miz1 is required for hair follicle structure and hair morphogenesis
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth