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Research 361–390 of 831
- Hyperadrenocorticism in Ferrets
- Darier Sign: A Historical Note
- Marie-unna hereditary hypotrichosis
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- The Role of Histone Demethylases in Disease
- Transcriptome Dynamics Reveal Stage-Specific and Melatonin-Triggered Gene Expression Patterns During The Cashmere Growth Cycle in Capra Hircus
- Distinct tooth regeneration systems deploy a conserved battery of genes
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Molecular genetics of androgen insensitivity
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Differential expression of steroid 5α-reductase isozymes and association with disease severity and angiogenic genes predict their biological role in prostate cancer
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- The genetic basis of dermatophytosis skin infection susceptibility
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Myotonic Dystrophy—A Progeroid Disease?
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Converging physiological roles of the anthrax toxin receptors