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Research 181–210 of 1000+
- Novel stain‐free lecithinized coal tar formulation for psoriasis
- Wound healing mechanism in Mongolian gerbil skin
- Bone morphogenetic protein signaling drives rete ridge morphogenesis: a distinct epidermal appendage program
- Defining the complex epithelia that comprise the canine claw with molecular markers of differentiation
- Ultrastructural visualization of cross-linked protein features in epidermal appendages
- Regulation of hard α-keratin mechanics via control of intermediate filament hydration: matrix squeeze revisited
- Wnt/β‐catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration
- Mitochondrial dysfunction as a cause of ageing
- Cloning of a Functional Vitamin D Receptor from the Lamprey (Petromyzon marinus), an Ancient Vertebrate Lacking a Calcified Skeleton and Teeth
- Low temperature abolishes human cellular circadian rhythm through Hopf bifurcation
- Human skin color: Origin, variation and significance
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- Feather arrays are patterned by interacting signalling and cell density waves
- Keratinization of sheath and calamus cells in developing and regenerating feathers
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Cornification in reptilian epidermis occurs through the deposition of keratin‐associated beta‐proteins (beta‐keratins) onto a scaffold of intermediate filament keratins
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Validation of Siddha Medicine in the Treatment of Alopecia areata in Paediatric Patient: A Case Report
- Hair follicle stem cells: A new arena
- 2P546 Structural Analysis of Curly and Straight Human Hair Fibers by Scanning Microbeam SAXS(52. Bio-imaging,Poster Session,Abstract,Meeting Program of EABS & BSJ 2006)
- Biology of the Hair Follicle: The Basics
- Hair loss