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- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless is a nuclear receptor corepressor essential for skin function
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Hairless: A nuclear receptor corepressor essential for skin function
- Catagen in the hairless house mouse
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- <i>Hoxc13</i> mutant mice lack external hair
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS