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Research 301–330 of 1000+
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Liposome-Based Carriers for CRISPR Genome Editing
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Cutaneous signals of immune system disease
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Dermal Adipocyte Lipolysis and Myofibroblast Conversion Are Required for Efficient Skin Repair
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Advances in single-cell transcriptomics in animal research
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- Polycystic Ovary Syndrome: Features, Diagnostic Criteria and Treatments
- Diseases of Periocular Hair
- Disorders of hair
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- The role of multiomics in revealing the mechanism of skin repair and regeneration
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Identification and Characterization of Two Se6OMTs from Stephania epigaea Offer Novel Insights into the Biosynthetic Pathway of Cepharanthine
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study