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Research 991–1000 of 1000+
- Ichthyosis
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Keratin gene mutations in disorders of human skin and its appendages
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix