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Research 481–510 of 846
- Olfactory receptor OR2AT4 regulates human hair growth
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Transcutaneous implantation of valproic acid-encapsulated dissolving microneedles induces hair regrowth
- Management of congenital ichthyoses: European guidelines of care, part two
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Compliance With Contraceptives and Other Treatments
- Maternal and neonatal hair mercury concentrations: the effect of dental amalgam
- Hair morphogenesis<i>in vitro</i>: formation of hair structures suitable for implantation
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Congenital hypotrichosis due to short anagen
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- Skin and hair: models for exploring organ regeneration
- One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
- Skin disease in pregnancy
- Adult epidermal Notch activity induces dermal accumulation of T cells and neural crest derivatives through upregulation of jagged 1
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Responses of hair follicle–associated structures to loss of planar cell polarity signaling
- Idiopathic CD4+ T-lymphocytopenia
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- The Genetics of Human Skin Disease
- Dermatological Manifestations of Stress in Normal and Psychiatric Populations
- Relating neurosteroid modulation of inhibitory neurotransmission to behaviour
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases