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Research 991–1000 of 1000+
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Actinic keratosis: a clinical and epidemiological revision
- Switching roles: the functional plasticity of adult tissue stem cells
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis