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Research 661–690 of 1000+
- Targeting IGF1‐Induced Cellular Senescence to Rejuvenate Hair Follicle Aging
- Comparative analysis of scalp and gut microbiome in androgenetic alopecia: A Korean cross-sectional study
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Squaric Acid Dibutylester Promotes Innate Immune-Driven Hair Growth with CD206+ Macrophage Accumulation in the Dermis
- Current Genetics in Hair Diseases
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Intermittent chronic telogen effluvium with an unusual dermoscopic finding following COVID ‐19
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Epidermal retinol dehydrogenases cyclically regulate stem cell markers and clock genes and influence hair composition
- Medical Dermatology
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Novel potential therapeutic targets of alopecia areata
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Development of Effervescent Cleansing Tablets Containing Asiatic-Acid-Loaded Solid Lipid Microparticles
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Trichoscopy in genetic hair shaft abnormalities
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Clinical cases of Darier-White follicular dyskeratosis
- Chronic delayed-type hypersensitivity reaction as a means to treat alopecia areata
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Bioengineered polyester nanoparticles for the synergistic treatment of androgenic alopecia via the suppression of 5α-reductase and knockdown of androgen receptor