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Research 61–90 of 72
- Direct conversion of mouse and human fibroblasts to functional melanocytes by defined factors
- Opposing impacts on healthspan and longevity by limiting dietary selenium in telomere dysfunctional mice
- Gastric cancer; actualities and perspectives of early diagnosis and targeted therapy
- Trichothiodystrophy
- Epithelial-Mesenchymal Micro-niches Govern Stem Cell Lineage Choices
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Implication of microRNA regulation in para-phenylenediamine-induced cell death and senescence in normal human hair dermal papilla cells
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- A Multifaceted View on Ageing of the Hair and Scalp
- Application of mesenchymal stem cells for anti-senescence and clinical challenges
- A Multidimensional Study Integrating Traditional Chinese Medicine and Network Pharmacology: Exploring the Skin Repair and Anti-Aging Effects of a Specific Combination of Five-Colored Plants
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- Genetic analysis of a novel antioxidant multi-target iron chelator, M30 protecting against chemotherapy-induced alopecia in mice
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Trichothiodystrophy: Current Concepts
- Trichothiodystrophy hair shafts display distinct ultrastructural features
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Progeroide Syndrome
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Histological and Gene Expression Analysis of the Effects of Menopause Status and Hormone Therapy on the Vaginal Introitus and Labia Majora