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Research 601–630 of 1000+
- Probiotics: An Adjuvant therapy for D-Galactose induced Alzheimer's disease
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Targeted delivery of siRNA to human cancer and human embryonic stem cells with cell level resolution
- <i>J. Cosmet. Sci., </i>59, 263–289 (July/August 2008) Characterization of curved hair of Japanese women with reference to internal structures and amino acid composition
- Regeneration of Epidermal and Dental Tissues, Lens and Cornea
- Using light to study sound: Stimulating hair cells with photonic pressure
- Nerve dependence in tissue, organ, and appendage regeneration
- SEXUAL DIMORPHISM IN MAMMALS
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Wound healing mechanism in Mongolian gerbil skin
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- 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
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- 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
- Validation of Siddha Medicine in the Treatment of Alopecia areata in Paediatric Patient: A Case Report
- Hair follicle stem cells: A new arena
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Highway Deconstruction
- Four Closure