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Research 121–150 of 1000+
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Low Humidity Alters Epidermal Gene Expression in vivo
- Sample collecting methods for bacterial community structure analysis of scalp hair: non-invasive swabbing versus intrusive hair shaft cutting
- Prostaglandin metabolism in human hair follicle
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Cell wall-associated ROOT HAIR SPECIFIC 10, a proline-rich receptor-like kinase, is a negative modulator of Arabidopsis root hair growth
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- A curated catalog of canine and equine keratin genes
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- 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
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- <i>In vivo</i>reprogramming of wound-resident cells generates skin with hair
- National scientific medical meeting 1996 abstracts
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Dermal Adipocyte Lipolysis and Myofibroblast Conversion Are Required for Efficient Skin Repair
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Immune modulation of hair follicle regeneration