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Research 391–420 of 1000+
- Monilethrix
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Acne Syndromes and Mosaicism
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- LB1034 Meta-analysis of scalp transcriptome defines alopecia areata subtypes and molecular response to four (4) treatments with jak inhibiting properties
- Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Identification and characterization of genes for skin and hair disorders
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters