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Research 511–540 of 1000+
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Prediction and Demonstration of Retinoic Acid Receptor Agonist Ch55 as an Antifibrotic Agent in the Dermis
- Gene trajectory inference for single-cell data by optimal transport metrics
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Psychological Stress-Induced Pathogenesis of Alopecia Areata: Autoimmune and Apoptotic Pathways
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Baseline Neutrophil-to-Lymphocyte Ratio Stratifies Early Trichoscopic Response to Platelet-Rich Plasma–Based Regimens in Non-Scarring Alopecia: A Real-World Cohort with Internal Validation Using an Interpretable Neural Network
- Where is the data? Delayed and chronic irAE surveillance and management after cessation of ICIs: expert insights from SITC on survivorship care and the need for long-term data
- Comprehensive single-cell transcriptomic profiling of the scalp from patients with moderate-to-severe alopecia areata
- SKPs Derive from Hair Follicle Precursors and Exhibit Properties of Adult Dermal Stem Cells
- O-Glycosylated Cell Wall Proteins Are Essential in Root Hair Growth
- Hyperactivation of sympathetic nerves drives depletion of melanocyte stem cells
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Commensal Microbes and Hair Follicle Morphogenesis Coordinately Drive Treg Migration into Neonatal Skin
- Targeting the Janus Kinase Family in Autoimmune Skin Diseases
- Male-pattern baldness susceptibility locus at 20p11
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Corticosterone inhibits GAS6 to govern hair follicle stem-cell quiescence
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- The dark art of light measurement: accurate radiometry for low-level light therapy
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Identification of Anabolic Selective Androgen Receptor Modulators with Reduced Activities in Reproductive Tissues and Sebaceous Glands
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits