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Research 391–420 of 1000+
- Potential mechanisms of exercise in maintaining skin homeostasis disrupted by protein deficiency (Review)
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- mRNA Levels of Aromatase, 5α-Reductase Isozymes, and Prostate Cancer-Related Genes in Plucked Hair from Young Men with Androgenic Alopecia
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Identification of immune microenvironment changes, immune-related pathways and genes in male androgenetic alopecia
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Transcriptomic Analysis Reveals Candidate Ligand-Receptor Pairs and Signaling Networks Mediating Intercellular Communication between Hair Matrix Cells and Dermal Papilla Cells from Cashmere Goats
- Transient skin stretching stimulates immune surveillance and promotes vaccine delivery via hair follicles
- Influence of Myosin Regulatory Light Chain and Myosin Light Chain Kinase on the Physiological Function of Inner Ear Hair Cells
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Minoxidil may suppress androgen receptor-related functions
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant