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Research 421–450 of 1000+
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Analogs of human genetic skin disease in domesticated animals
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Differences between ultrastructure and protein composition in straight hair fibres
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Beyond the Hot Comb: Updates in Epidemiology, Pathogenesis, and Treatment of Central Centrifugal Cicatricial Alopecia from 2011 to 2021
- Use of dermoscopy in the diagnosis of temporal triangular alopecia
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Real-World Outcomes and Healthcare Utilization of Lanadelumab in Spain: Insights from First Cohort of Difficult-to-Treat Hereditary Angioedema Cases
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- Lichen Planopilaris
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Genetic Basis of Male Pattern Baldness
- Hair follicle-specific keratins and their diseases
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Trichoscopy in genetic hair shaft abnormalities
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms