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Research 901–930 of 1000+
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Beyond Wavy Hairs
- Genetic Disorders and Defects in Vitamin D Action
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Inhibition of JAK-STAT Signaling with Baricitinib Reduces Inflammation and Improves Cellular Homeostasis in Progeria Cells
- Primary cicatricial alopecia: diagnosis and treatment
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Erythromelanosis follicularis faciei in women
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- New developments in the molecular treatment of ichthyosis: review of the literature
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Difficult and rare forms of acne
- Acrodermatitis Enteropathica‐like Eruption in an Infant with Nonketotic Hyperglycinemia
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction