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Research 721–750 of 1000+
- Pathological and Biochemical Studies on Experimental Hypothyroidism in Growing Lambs
- The development of an in vitro human hair follicle organoid with a complexity similar to that in vivo
- Pilomatricoma can differentiate not only towards hair matrix and hair cortex, but also follicular infundibulum, outer root sheath and hair bulge
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Enrichment for Living Murine Keratinocytes from the Hair Follicle Bulge with the Cell Surface Marker CD34
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Proteome Analysis of Human Hair Shaft
- Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Treatment of Pseudofolliculitis With a Pulsed Infrared Laser
- Disruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
- The regulation of skin homeostasis, repair and the pathogenesis of skin diseases by spatiotemporal activation of epidermal mTOR signaling
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The Localization of Label-Retaining Cells in Eccrine Glands
- Isolation of intermediate filament assemblies from human hair follicles.
- In situ labeling of DNA reveals interindividual variation in nuclear DNA breakdown in hair and may be useful to predict success of forensic genotyping of hair
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- The mineralocorticoid receptor plays a transient role in mouse skin development
- Desmosomes in Developing Human Epidermis
- Pyruvate Kinase M2 Accelerates Cutaneous Wound Healing via Glycolysis and Wnt/β-Catenin Signaling
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Preparing the hair follicle canal for hair shaft emergence