Search
for
Sort by
Research 61–90 of 172
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- A novel and safe small molecule enhances hair follicle regeneration by facilitating metabolic reprogramming
- Hair Shaft Dysplasias
- Stimulation of elastin expression by minoxidil in chick skin fibroblasts
- Congenital atrichia and hypotrichosis
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Molecular functional analyses revealed essential roles of HSP90 and lamin A/C in growth, migration, and self-aggregation of dermal papilla cells
- Cell Density-Dependent Upregulation of PDCD4 in Keratinocytes and Its Implications for Epidermal Homeostasis and Repair
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- Physiology and Medical Treatments for Alopecia
- Diseases of Periocular Hair
- Acquired Uncombable Hair
- Causality of Aging Hallmarks
- Perspectives on Dermatopathology
- Skin aging: mechanisms, evaluation, and rejuvenation
- Bhangra: Therapeutic and Pharmacological Actions in Shayb (Premature Greying of Hair)
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- The Ayurvedic Management in Graying of Hair
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Irradiation-induced hair graying in mice: an experimental model to evaluate the effectiveness of interventions targeting oxidative stress, DNA damage prevention, and cellular senescence
- Signaling pathways in hair aging
- The study of premature canities and its association in tertiary care hospital
- Hair Loss in Children
- Historical Archives
- Syndromes of Severe Insulin Resistance (SSIRs)
- Werner′s syndrome
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Congenital atrichia associated with nevus flammeus: A rare association