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Research 91–120 of 1000+
- Profiling of hair proteome revealed individual demographics
- Myotonic Dystrophy—A Progeroid Disease?
- Protective Role of Melatonin and Its Metabolites in Skin Aging
- Genetically separable determinants of hair keratin gene expression
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Premature Senescence of Balding Dermal Papilla Cells In Vitro Is Associated with p16INK4a Expression
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- The composition of cell‐based therapies obtained from point‐of‐care devices/systems which mechanically dissociate lipoaspirate: a scoping review of the literature
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Cellular senescence and polycystic ovary syndrome: mechanisms and therapeutic strategies from a new perspective
- Skin-specific transgenic overexpression of ovine β-catenin in mice
- Genotoxic Agents: An Unexpected Effect on Healthy Epithelia
- L-Cystine-Containing Hair-Growth Formulation Supports Protection, Viability, and Proliferation of Keratinocytes
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Epidermal/Dermal Separation Techniques and Analysis of Cell Populations in Human Skin Sheets
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Applications of Exosomal miRNAs from Mesenchymal Stem Cells as Skin Boosters
- Editor's evaluation: Role of distinct fibroblast lineages and immune cells in dermal repair following UV radiation-induced tissue damage
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature