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Research 511–540 of 1000+
- Defining Hair Follicles in the Age of Stem Cell Bioengineering
- Real-time <i>in vivo</i> structure-function study of scalp hair cycles: an experimental approach for monitoring living hair roots with a 20-year follow-up
- Epidermal stem cells and skin tissue engineering in hair follicle regeneration
- <i>Malva verticillata</i>seed extracts upregulate the Wnt pathway in human dermal papilla cells
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Stability of opiates in hair fibers after exposure to cosmetic treatment
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Efficacy and Safety of a Drinkable Nutraceutical in Premenopausal Women with Telogen Effluvium: A 6-Month, Randomized, Multicenter, Double-Blind, Placebo-Controlled Study
- Induction of synapse associated protein 102 expression in cyclosporin A-stimulated hair growth
- Enhancing Permeation of Drug Molecules Across the Skin via Delivery in Nanocarriers: Novel Strategies for Effective Transdermal Applications
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bio‐active designed peptide for hair keratin strengthening
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- New keratin isolates: actives for natural hair protection.
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- Four murine monoclonal antibodies specific for the inner root sheath in the human hair follicle
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- In vitro induction of hair follicle signatures using human dermal papilla cells encapsulated in fibrin microgels
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Single-cell transcriptomics reveals lineage trajectory of human scalp hair follicle and informs mechanisms of hair graying
- Growth Hormone Operates as a Neuroendocrine Regulator of Human Hair Growth Ex Vivo
- Strain and Strain Recovery of Human Hair from the Nano- to the Macroscale
- Metal doped keratin film standard for LA-ICP-MS determination of lead in hair samples
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Human Hair and the Impact of Cosmetic Procedures: A Review on Cleansing and Shape-Modulating Cosmetics
- Isolation of a Novel Population of Multipotent Adult Stem Cells from Human Hair Follicles
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo