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Research 901–930 of 1000+
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Beta Human Papillomavirus and Merkel Cell Polyomavirus in Skin Neoplasms
- Second International Symposium—Epigenetic Regulation of Skin Regeneration and Aging: From Chromatin Biology towards the Understanding of Epigenetic Basis of Skin Diseases
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Skin Stearoyl-CoA Desaturase Genes
- Fast Motions in 5 Alpha Reductase and Its Impact on Enzyme Kinetics
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages
- 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
- Netherton Syndrome – Responding to Oral Retinoids
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Wokeness in Our Practice
- Male androgenetic alopecia
- Evaluation of the Hair Growth-Promoting Effects of Combined Treatment with Hair Growth Stimulants
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Cell death as an architect of adult skin stem cell niches
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review