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Research 241–270 of 668
- Targeting integrin pathways: mechanisms and advances in therapy
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Extracellular Vesicles: Emerging Therapeutics in Cutaneous Lesions
- Regulation of stem cell fate by HSPGs: implication in hair follicle cycling
- Reversing Gray Hair: Inspiring the Development of New Therapies Through Research on Hair Pigmentation and Repigmentation Progress
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Interdisciplinarity traditional Chinese medicine microneedles in skin disease treatment: Recent advances and challenges
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Hair Follicle Signaling Networks: A Dermal Papilla–Centric Approach
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Keratinocyte Stem Cells: Role in Aging
- Transcranial Red LED Therapy: A Promising Non-Invasive Treatment to Prevent Age-Related Hippocampal Memory Impairment
- Exosomes derived stem cells as a modern therapeutic approach for skin rejuvenation and hair regrowth
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- E-Poster
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- The Anti-atopic Lotions Containing Fucoidan Extracted from Ecklonia Cava Impact on Hairless Mice Atopic Dermatitis Skin
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Phospholipase C‐δ1 is an essential molecule downstream of <i>Foxnl,</i> the gene responsible for the nude mutation, in normal hair development
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Phospholipase A<sub>2</sub> inhibition as potential therapy for inflammatory skin diseases
- Phospholipase's role in maintaining and restoring skin and hair health
- Loss of adipocyte phospholipase gene PLAAT3 causes lipodystrophy and insulin resistance due to inactivated arachidonic acid-mediated PPARγ signaling
- Integrated Lipidomics in the Secreted Phospholipase A2 Biology