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Research 181–210 of 1000+
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Making the head: Caspases in life and death
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- The developmental basis of fingerprint pattern formation and variation
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Madarosis: A marker of many Maladies
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Palatogenesis and cutaneous repair: A two‐headed coin
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Hair & Cutaneous Development
- Tissue engineering of skin and regenerative medicine for wound care
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review
- Eyes open on stem cells
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Bioengineered skin organoids: from development to applications
- Subject Index
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Cell death as an architect of adult skin stem cell niches
- SOX9 in organogenesis: shared and unique transcriptional functions
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family