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Research 691–720 of 1000+
- Alopezien und Hypotrichosen im Kindesalter
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Molecular Evolution and Protein Structure Variation of Dkk Family
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- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Remodelling of cytoskeleton and plasma membrane proteins contributes to drought sensitivity of Arabidopsis<i>rhd2</i>mutant
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Snail2: Estudios estructura-función y análisis in vivo de su papel en el desarrollo del folícullo piloso y la carcinogénesis química de la piel
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- The Catalog of Human Hair Keratins
- Hyperactivation of sympathetic nerves drives depletion of melanocyte stem cells
- Evidence that Myc activation depletes the epidermal stem cell compartment by modulating adhesive interactions with the local microenvironment
- Fundamental hair follicle biology and fine fibre production in animals
- Noninvasive method for assessing the human circadian clock using hair follicle cells
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Hair follicle immune privilege and its collapse in alopecia areata
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Cell fate decisions: emerging roles for metabolic signals and cell morphology