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Research 61–90 of 1000+
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- 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
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hair loss and its management in children
- Follistatin and secreted frizzled-related protein 1, OVO homolog-like 1-regulated genes, are important for hair follicle neogenesis
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Aging and Anti-Aging in Hair and Hair Loss
- The Role of Histone Demethylases in Disease
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Alopecias
- Hair follicles and their role in skin health
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Hair That Is Difficult to Manage in a Hispanic Girl
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Primary cicatricial alopecia: diagnosis and treatment
- Madarosis: A marker of many Maladies
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Diseases of Hair
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Comparative immunohistochemical analysis suggests a conserved role of EPS8L1 in epidermal and hair follicle barriers of mammals