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Research 31–60 of 1000+
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- 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
- Establishment of an in vitro hairless guinea pig dermal model
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- A novel hairless highly immunodeficient mice model optimized for in vivo imaging
- Abstract 5020: Characterization of epidermal stem cells in SKH1 hairless mice, a widely used mouse model to investigate ultraviolet radiation carcinogenesis.
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Molecular basis of congenital atrichia in humans and mice.
- Alopecia: Association with Resistance to Thyroid Hormones
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- In This Issue
- Learning from nudity: lessons from the nude phenotype
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Disease causing homozygous variants in the human hairless gene
- Analyzing the innate immunity of NIH hairless mice and the impact of gut microbial polymorphisms on<i>Listeria monocytogenes</i>infection
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Hairless is a nuclear receptor corepressor essential for skin function
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes