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Research 31–60 of 41
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Congenital atrichia with papular lesions
- Atrichia with papular lesions
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Off-label uses of retinoids in dermatology
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- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Normalization of testosterone levels using a low estrogen-containing oral contraceptive in women with polycystic ovary syndrome.
- Implications of Non-compliance in the Management of Chronic Polycystic Ovarian Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
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- Hormonal contraceptives: pharmacology tailored to women's health
- Pharmacologic Therapy of Polycystic Ovary Syndrome
- CLINICAL UPDATES IN HAIR
- Steroid Hormones of Reproduction and Sexual Development
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Dermatopathology and molecular genetics
- Congenital atrichia and hypotrichosis
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions