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Research 31–60 of 36
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Molecular Mechanisms Regulating Hair Follicle Development
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- SOX18 Promotes the Proliferation of Dermal Papilla Cells via the Wnt/β-Catenin Signaling Pathway
- Recently Identified Forms of Epidermolysis Bullosa
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Natural variation in trichome density and biochemistry in Antirrhinum
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Alopecia Areata
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Responses of hair follicle–associated structures to loss of planar cell polarity signaling
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Frizzled Receptors in Development and Disease
- Developmental genetics of color pattern establishment in cats
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- TRPV3 Ion Channel: From Gene to Pharmacology
- Poster Presentations