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Research 451–480 of 1000+
- Efficacy of Ritlecitinib in Patients with Alopecia Areata by Extent of Hair Loss: Results from the Phase 2b/3 and Phase 3 ALLEGRO Clinical Trials
- Distribution of SALT Scores with Ritlecitinib Treatment up to 24 months from the ALLEGRO Phase 2b/3 and Long-Term Phase 3 Clinical Studies in Alopecia Areata
- Sustained Scalp, Eyebrow, and Eyelash Hair Regrowth with Ritlecitinib Through Week 48 in Patients with Alopecia Areata: Post-Hoc Analysis of the ALLEGRO Phase 2b/3 Study
- Alopecia areata: Ritlecitinib generates substantial re-growth of scalp hair
- Cholesterol homeostasis in hair follicle keratinocytes is disrupted by impaired ABCA5 activity
- Possible Cellular Communication with Human Follicle Dermal Papilla Cells via Secretions from Human Hair Follicle Keratinocytes
- The Role of ATP-dependent Chromatin Remodeling in the Control of Epidermal Differentiation and Skin Stem Cell Activity
- Editors' Picks
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- Influence of feed restriction on the wool proteome: A combined iTRAQ and fiber structural study
- Visible-to-Near IR Quantum Dot–Based Hypermulticolor High-Content Screening of Herbal Medicines for the Efficacy Monitoring of Hair Growth Promotion and Hair Loss Inhibition
- Keratin Gene Expression in Wool Fibre Development
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Abstracts
- Economic disparities in parental hair cortisol are associated with externalizing behavior in children
- An intrafamilial transmission of<i>Arthroderma benhamiae</i>in Canadian porcupines (<i>Erethizon dorsatum</i>) in a Japanese zoo
- Alopecia: Association with Resistance to Thyroid Hormones
- [Monilethrix--rare syndrome of structural hair abnormalities].
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- How to defeat male pattern alopecia in a trompeur de femmes, who loves to abuse of libido boosters?
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Association of Frailty Index with Clinical BPH Progression and Serious Adverse Events: the MTOPS Trial
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Notes from the Editors Emeritus
- Prodrugs of butyric acid from bench to bedside: Synthetic design, mechanisms of action, and clinical applications
- Acrodermatitis Enteropathica
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Disease causing homozygous variants in the human hairless gene