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Research 30 of 1000+
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- 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>)
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Effect of Carbamates on mRNA Encoding Lipid Enzymes in Hamster Flank Organs
- Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless is a nuclear receptor corepressor essential for skin function
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Disease causing homozygous variants in the human hairless gene
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Vitamin D metabolism and function in the skin
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Biology and Genetics of Hair
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- 3-Deoxysappanchalcone Promotes Proliferation of Human Hair Follicle Dermal Papilla Cells and Hair Growth in C57BL/6 Mice by Modulating WNT/β-Catenin and STAT Signaling
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Hairless controls hair fate decision via Wnt/β–catenin signaling