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Research 211–240 of 1000+
- Hair Follicle Stem Cell Faith Is Dependent on Chromatin Remodeling Capacity Following Low-Dose Radiation
- TLR9 activation in large wound induces tissue repair and hair follicle regeneration via γδT cells
- Cellular senescence and polycystic ovary syndrome: mechanisms and therapeutic strategies from a new perspective
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- Cell‐free transcriptomic profiles and mechanism insights in female androgenetic alopecia
- Melatonin: A Cutaneous Perspective on its Production, Metabolism, and Functions
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Genetically separable determinants of hair keratin gene expression
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- PBX1-SIRT1 Positive Feedback Loop Attenuates ROS-Mediated HF-MSC Senescence and Apoptosis
- L-Cystine-Containing Hair-Growth Formulation Supports Protection, Viability, and Proliferation of Keratinocytes
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Do Changes in Chromosomes Cause Aging?
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- MSCs and their exosomes: a rapidly evolving approach in the context of cutaneous wounds therapy
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Proposed mechanisms of low-level light therapy in the treatment of androgenetic alopecia
- Australasian Society for Dermatology Research Meeting, May 2006
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- The Role of Histone Demethylases in Disease
- Structure of human type II 5 alpha-reductase gene.
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Chapter 23. Therapeutic Control of Androgen Action
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions