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Research 421–450 of 1000+
- White piedra and pediculosis capitis in the same patient
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Efficacy and safety of SGLT2 inhibitor on insulin resistance and hyperglycemia in Werner syndrome—A case report
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Over-, ectopic-expression of FoxN1 at early life adversely influences lymphopoiesis (HEM3P.280)
- FoxN1 in K14 promoter-driven epithelium is required for generation and maintenance of 3D-thymus medulla and preventing nude phenotype in the skin (36.33)
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Autophagy critically controls skin inflammation and apoptosis-induced stem cell activation
- Autotaxin-LPA signaling contributes to obesity-induced insulin resistance in muscle and impairs mitochondrial metabolism
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Congenital atrichia with papular lesions
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Zinc and Zinc Transporters in Dermatology
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Molecular Genetics of Human Hair Diseases
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes