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Research 61–90 of 1000+
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Dermatopathology and molecular genetics
- 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
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Le gène<i>hairless</i>de la souris
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Hairless: A nuclear receptor corepressor essential for skin function
- Hair Today
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- The character “hairless” in the mouse
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Hairless protein of Jumonji family and hair loss
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless is a nuclear receptor corepressor essential for skin function
- Increased rate of hair keratin gene loss in the cetacean lineage
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Genetics of Alopecia