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Research 451–480 of 1000+
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Genetics of Structural Hair Disorders
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Cheating on forensic hair testing? Detection of potential biomarkers for cosmetically altered hair samples using untargeted hair metabolomics
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Molecular Genetics of Alopecias
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Alopecia: Association with Resistance to Thyroid Hormones
- Disease causing homozygous variants in the human hairless gene
- The Mammalian Hairless Protein as a DNA Binding Phosphoprotein
- Diagnostic Value of VDR in Bone Metastasis and Prognosis of Patients with Breast Cancer and Expression Correlation between Vitamin D Receptor and Hairless Protein
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Commentary on: Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus