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Research 871–900 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Acne, the Skin Microbiome, and Antibiotic Treatment
- Feather arrays are patterned by interacting signalling and cell density waves
- Identifying the Target Cells and Mechanisms of Merkel Cell Polyomavirus Infection
- dsRNA Released by Tissue Damage Activates TLR3 to Drive Skin Regeneration
- Human Scalp Hair Follicles Are Both a Target and a Source of Prolactin, which Serves as an Autocrine and/or Paracrine Promoter of Apoptosis-Driven Hair Follicle Regression
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- 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
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Intestinal Dysbiosis and Biotin Deprivation Induce Alopecia through Overgrowth of Lactobacillus murinus in Mice
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Prostaglandin metabolism in human hair follicle
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Fadrozole and finasteride exposures modulate sex steroid- and thyroid hormone-related gene expression in Silurana (Xenopus) tropicalis early larval development
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- The prostamide‐related glaucoma therapy, bimatoprost, offers a novel approach for treating scalp alopecias
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- High proliferation and delamination during skin epidermal stratification