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Research 91–120 of 1000+
- Hair loss
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Parathyroid hormone-related peptide and the hair cycle - is it the agonists or the antagonists that cause hair growth?
- 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
- Bone morphogenetic protein signaling drives rete ridge morphogenesis: a distinct epidermal appendage program
- Potential of silk proteins in cosmetics
- Hair removal using an Nd: YAG laser system.
- Hair Loss Diagnosis Using Artificial Neural Networks
- Hair and Scalp Disorders in Women of African Descent
- Serum levels of minerals and vitamins in two categories of female alopecia subjects using hair relaxer
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- Causes of hair loss and the developments in hair rejuvenation
- Follistatin and secreted frizzled-related protein 1, OVO homolog-like 1-regulated genes, are important for hair follicle neogenesis
- Circadian rhythms on skin function of hairless rats: light and thermic influences
- Topical Gene Electrotransfer to the Epidermis of Hairless Guinea Pig by Non-Invasive Multielectrode Array
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Wnt signaling in skin organogenesis
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Biology and Genetics of Hair
- Learning from nudity: lessons from the nude phenotype
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Convergent Evolution of Cysteine-Rich Keratins in Hard Skin Appendages of Terrestrial Vertebrates
- Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation