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Research 151–180 of 375
- Mechanical force drives the initial mesenchymal-epithelial interaction during skin organoid development
- Scalable and high-throughput production of an injectable platelet-rich plasma (PRP)/cell-laden microcarrier/hydrogel composite system for hair follicle tissue engineering
- Serum level of Alarin in Patients with Androgenetic Alopecia
- Influence of Ethnic Origin of Hair on Water-Keratin Interaction . . . . . . . . . . . . . . . . . . . . . . . Alain Franbourg, Fre´de´ric Leroy, Marielle Escoube´s, and
- 706 Predictive modeling of patient response to JAK/STAT inhibitors and dynamic patient-matching
- Botanical extracts
- Endocrine and Intracrine Sources of Androgens in Women: Inhibition of Breast Cancer and Other Roles of Androgens and Their Precursor Dehydroepiandrosterone
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Canonical WNT signaling promotes mammary placode development and is essential for initiation of mammary gland morphogenesis
- Guidelines for the management of vitiligo: the European Dermatology Forum consensus
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Keratins of the human hair follicle: “Hyperproliferative” keratins consistently expressed in outer root sheath cells in vivo and in vitro
- Treatment of hirsutism with the pure antiandrogen flutamide
- First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
- Successful Treatment of Chronic Leg Ulcers with Epidermal Equivalents Generated from Cultured Autologous Outer Root Sheath Cells
- Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa
- New clinico‐genetic classification of trichothiodystrophy
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Soluble factors from human hair papilla cells and dermal fibroblasts dramatically increase the clonal growth of outer root sheath cells
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Characteristics of Men Who Report Persistent Sexual Symptoms After Finasteride Use for Hair Loss
- Skin physiology in microgravity: a 3-month stay aboard ISS induces dermal atrophy and affects cutaneous muscle and hair follicles cycling in mice
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Keratins 1 and 10 or homologues as regular constituents of inner root sheath and cuticle cells in the human hair follicle.
- Modulation of the differentiated phenotype of keratinocytes of the hair follicle and from epidermis
- Interest of High-Dose Pulse Corticosteroid Therapy Combined with Methotrexate for Severe Alopecia Areata: A Retrospective Case Series
- Proteomic tools for the investigation of human hair structural proteins and evidence of weakness sites on hair keratin coil segments
- Beyond vitiligo guidelines: combined stratified/personalized approaches for the vitiligo patient
- Outer root sheath (ORS) cells organize into epidermoid cyst-like spheroids when cultured inside Matrigel: a light-microscopic and immunohistological comparison between human ORS cells and interfollicular keratinocytes