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Research 91–120 of 650
- Exossomos na Dermatologia: revisão de sua ação em doenças cutâneas e rejuvenescimento
- Recent Trends and Future Prospects of Phytosomes: A Concise Review
- Perioperative Care of the Surgical Patient
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Sebum Free Fatty Acids Enhance the Innate Immune Defense of Human Sebocytes by Upregulating β-Defensin-2 Expression
- The Association of Hispanic Ethnicity with Nonalcoholic Fatty Liver Disease in Polycystic Ovary Syndrome
- CRISPR/Cas9: A Promising Approach for Alopecia
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Recent advances in the epidermal growth factor receptor/ligand system biology on skin homeostasis and keratinocyte stem cell regulation
- Gab1 and Mapk Signaling Are Essential in the Hair Cycle and Hair Follicle Stem Cell Quiescence
- Clinicopathological factors associated with trichilemmal cysts
- eLife assessment: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Hair Follicle Signaling Networks: A Dermal Papilla–Centric Approach
- Recent Advances in the Electro-Active Therapeutic Phytochemical-Based Sensors
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Prostaglandins: Key players in immunomodulation of the nervous system
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- 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