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Research 121–150 of 1000+
- Disease causing homozygous variants in the human hairless gene
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Distinct tooth regeneration systems deploy a conserved battery of genes
- ROR2 regulates self-renewal and maintenance of hair follicle stem cells
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The Genetics of Human Skin Disease
- What causes hidradenitis suppurativa ?—15 years after
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Biochemistry of epidermal stem cells
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Generalised Glucocorticoid Resistance
- <i>Hoxc13</i> mutant mice lack external hair
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development