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Research 61–90 of 1000+
- Dermatological aspects of primary psychiatric disorders
- Rand Protease: The Role of Calcium-Binding Site on Stability with Mutagenesis and The Effectiveness on Leather Dehairing
- 1452 Noncoding dsRNA stimulates exosome biosynthesis to regulate skin regeneration
- 851 The role of astrotactin2 in regulating mammalian skin polarity
- Etoposide sensitizes CT26 colorectal adenocarcinoma to radiation therapy in BALB/c mice
- Endocrine and Intracrine Sources of Androgens in Women: Inhibition of Breast Cancer and Other Roles of Androgens and Their Precursor Dehydroepiandrosterone
- Is dehydroepiandrosterone a hormone?
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Guidelines for the management of vitiligo: the European Dermatology Forum consensus
- North American clinical management guidelines for hidradenitis suppurativa: A publication from the United States and Canadian Hidradenitis Suppurativa Foundations
- 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
- Development of a Chitosan Nanofibrillar Scaffold for Skin Repair and Regeneration
- Androgen biosynthetic pathways in the human prostate
- 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
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Pathology of Mouse Models of Accelerated Aging
- 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
- French administrative health care database (SNDS): The value of its enrichment
- 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
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Use of high dose cyproterone acetate and risk of intracranial meningioma in women: cohort study
- 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