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- Alopecia totalis in an infant
- 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.
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Molecular Genetics of Alopecias
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Congenital hair loss disorders: Rare, but not too rare
- Disease causing homozygous variants in the human hairless gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- Clinical and molecular genetic studies in hereditary hair loss
- Congenital Atrichia: A Case Report
- Papular atrichia
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Genetics of Structural Hair Disorders