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Research 61–90 of 1000+
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Disease causing homozygous variants in the human hairless gene
- Defining compartmentalized stem and progenitor populations with distinct cell division frequency in the ocular surface epithelium
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Clinical and molecular genetic studies in hereditary hair loss
- Horse hair follicles: A novel dermal stem cell source for equine regenerative medicine
- Defining the identity of mouse embryonic dermal fibroblasts
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Hair Protein Polymorphism and Its Application to Forensic Science Hair Comparison.
- Decision letter: Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- The Enzymic Derivation of Citrulline Residues from Arginine Residues In Situ during the Biosynthesis of Hair Proteins that are Cross-Linked by Isopeptide Bonds
- Tenascin-C expressing touch dome keratinocytes exhibit characteristics of all epidermal lineages
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Identification of hair shaft progenitors that create a niche for hair pigmentation
- Ox40-Cre–mediated deletion of BRD4 reveals an unexpected phenotype of hair follicle stem cells in alopecia
- Decision letter: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- Epigenetic control of skin and hair regeneration after wounding
- The River of Stem Cells
- Are fingernails a key to unlocking the puzzle of mammalian limb regeneration?
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- ToF‐SIMS characterization of the lipid layer on the hair surface. I: the damage caused by chemical treatments and UV radiation
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Clonal analysis of stem cells in differentiation and disease