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Research 91–120 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Congenital atrichia with papular lesions
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Current Genetics in Hair Diseases
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Atrichia with papular lesions
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Comparative Spatial Transcriptomic and Single-Cell Analyses of Human Nail Units and Hair Follicles Show Transcriptional Similarities between the Onychodermis and Follicular Dermal Papilla
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals