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Research 871–900 of 1000+
- The The Relationships Among Routes of Transmissions, Environmental Factors Tolerance and Mutation Rates of Some RNA Viruses
- 42863 The association of milia-like calcinosis cutis, alopecia totalis and hyperthyroidism linked with the novel mutation for RBM28
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Molecular basis of androgen insensitivity
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Building Epithelial Tissues from Skin Stem Cells
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Congenital hair loss disorders: Rare, but not too rare
- The nude gene and the skin
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Gsdma3 is required for hair follicle differentiation in mice
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Biochemistry of epidermal stem cells
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Characterization of Human Keratin-Associated Protein 1 Family Members
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome
- Genetic Basis of Pigmentation and Its Disorders
- Disease causing homozygous variants in the human hairless gene
- High-resolution structures of mutants of residues that affect access to the ligand-binding cavity of human lipocalin-type prostaglandin D synthase
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Tradescantia-Based Test Systems Can Be Used for the Evaluation of the Toxic Potential of Harmful Algal Blooms