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Research 31–60 of 1000+
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- A mutation in MAP2 is associated with prenatal hair follicle density
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hair Today
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- The character “hairless” in the mouse
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Disease causing homozygous variants in the human hairless gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- To be hairless or wise?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Alopecia: Association with Resistance to Thyroid Hormones
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Alopecia totalis in an infant
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- Towards Defining the Pathogenesis of the Hairless Phenotype
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- Hairless controls hair fate decision via Wnt/β–catenin signaling