Search
for
Sort by
Research 181–210 of 1000+
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Expression of truncated latent TGF-β-binding protein modulates TGF-β signaling
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Chapter 23. Therapeutic Control of Androgen Action
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Structural optimization of pep7, a small peptide extracted from epimorphin, for effective induction of hair follicle anagen
- Inherited Disorders of the Hair
- Androgen Receptor Ligands: Agonists and Antagonists
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Learning from nudity: lessons from the nude phenotype
- Androgen receptors and their biology
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Diagnostic approach to low‐renin hypertension