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Research 841–870 of 1000+
- Role of neurosteroids in the anticonvulsant activity of midazolam
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Stiffness of Human Hair Correlates with the Fractions of Cortical Cell Types
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- The biology and genetics of curly hair
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Bioinformatics analysis and verification of m6A related genes based on the construction of keloid diagnostic model
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- 4 Anti-androgens in gynaecological practice
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- MicroRNA-181a Targets GNAI2 and Affects the Proliferation and Induction Ability of Dermal Papilla Cells: The Potential Involvement of the Wnt/β-Catenin Signaling Pathway
- Identification of differentially expressed Gnαs and Gnα11 in sheep ( Ovis aries ) skins associated with white and black coat colors
- The citrullinating enzyme PADI4 governs progenitor cell proliferation and translation in developing hair follicles
- Ectoin attenuates cortisone‐induced skin issues by suppression GR signaling and the UVB‐induced overexpression of 11β‐HSD1
- The Interplay between Finasteride-Induced Androgen Imbalance, Endoplasmic Reticulum Stress, Oxidative Stress, and Liver Disorders in Paternal and Filial Generation
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- 1329 CENPV is a novel CYLD-interacting molecule regulating ciliary acetylated tubulin
- Activating Wnt/β-catenin signaling pathway for disease therapy: Challenges and opportunities
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Noggin overexpression inhibits eyelid opening by altering epidermal apoptosis and differentiation
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Over-expression of TSPO in the hippocampal CA1 area alleviates cognitive dysfunction caused by lipopolysaccharide in mice
- Introduction—Human Hair, Skin, and Hair Care Products
- Homology Modeling of 5-alpha-Reductase 2 Using Available Experimental Data
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Salvianolic acid B ameliorate alopecia by simultaneously targeting Wnt/β-catenin and mTORC2/Akt signaling
- Treatment of androgenetic alopecia by exosomes secreted from hair papilla cells and the intervention effect of LTF
- Cholesterol homeostasis in hair follicle keratinocytes is disrupted by impaired ABCA5 activity
- Lactium: A Novel Drug for Psychocutaneous Skin Disorders