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Research 511–540 of 1000+
- ERUCA SATIVA LINN.: PHARMACOGNOSTICAL AND PHARMACOLOGICAL PROPERTIES AND PHARMACEUTICAL PREPARATIONS
- Functional characterization of soybean strigolactone biosynthesis and signaling genes in Arabidopsis MAX mutants and GmMAX3 in soybean nodulation
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- A kindred with mutant IKAROS and autoimmunity
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Manipulation of outer root sheath cell survival perturbs the hair-growth cycle
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Genetically separable determinants of hair keratin gene expression
- PKC downregulation upon rapamycin treatment attenuates mitochondrial disease
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Sesn2/AMPK/mTOR signaling mediates balance between survival and apoptosis in sensory hair cells under stress
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Developmental genetics of color pattern establishment in cats
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Tabby pattern genetics – a whole new breed of cat
- The protease corin regulates electrolyte homeostasis in eccrine sweat glands
- Semidominant Inheritance in Epidermolytic Ichthyosis
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- ROBO4 deletion ameliorates PAF-mediated skin inflammation via regulating the mRNA translation efficiency of LPCAT1/LPCAT2 and the expression of PAF receptor
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations