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Research 31–60 of 1000+
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Genetics of Structural Hair Disorders
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Congenital hypotrichosis due to short anagen
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Molecular Genetics of Alopecias
- Alopezien und Hypotrichosen im Kindesalter
- Hair Shaft Dysplasias
- Congenital hair loss disorders: Rare, but not too rare
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetic Hair Disorders: A Review
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Diseases of Periocular Hair
- Follistatin and secreted frizzled-related protein 1, OVO homolog-like 1-regulated genes, are important for hair follicle neogenesis
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair Loss in Children
- A spermidine-based nutritional supplement prolongs the anagen phase of hair follicles in humans: a randomized, placebo-controlled, double-blind study
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- The Role of Histone Demethylases in Disease
- Hair follicles and their role in skin health
- Secondary cicatricial and other permanent alopecias
- Hair loss in infancy and childhood
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Hairless is a nuclear receptor corepressor essential for skin function
- 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