Search
for
Sort by
Research 841–870 of 1000+
- Primary cicatricial alopecia: diagnosis and treatment
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride
- 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
- Converging physiological roles of the anthrax toxin receptors
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A rare case of woolly hair with unusual associations
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Testosterone regulates levels of cystic fibrosis transmembrane regulator, adenylate cyclase, and cAMP in the seminal vesicles of orchidectomized rats
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review