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Research 421–450 of 1000+
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Thermodynamically stable ionic liquid microemulsions pioneer pathways for topical delivery and peptide application
- The potential of androgenic alopecia management from plant derivatives
- Metabolomic analysis of SMP30/GNL knockout mice treated with fermented vegetable and fruit extract (OM-X®)
- Overview of the Circadian Clock in the Hair Follicle Cycle
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- 832 Variability in secretion of growth factors by platelets is intrinsic to alopecia patients undergoing platelet-rich plasma therapy
- Laser capture microdissection as a method for investigating the human hair follicle microbiome reveals region-specific differences in the bacteriome profile
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Oncogenic senescence: a multi-functional perspective
- Ottawa, Ontario, Canada, February 13–16, 2013
- Scarring Alopecia
- The role of androgen therapy
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- An Ayurvedic & Contemporary Perspective on a Comprehensive Appraisal of Ageing
- Acquired scalp alopecia. Part I: A review
- Hormesis and medicine
- Effects of PNU157706, a Dual 5α-Reductase Inhibitor, on Rat Epididymal Sperm Maturation and Fertility1
- Morphological characteristics and notes of the skin in preclinical toxicity assessment
- 0882 Patterning and regional specification of hairy skin
- Evolution in action: highlighting a role for the Agouti gene in development?
- FOXN1 deficient nude severe combined immunodeficiency
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Common Forms of Congenital Adrenal Hyperplasia
- A kindred with mutant IKAROS and autoimmunity
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex