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Research 691–720 of 1000+
- p63: a crucial player in epithelial stemness regulation
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- ERUCA SATIVA LINN.: PHARMACOGNOSTICAL AND PHARMACOLOGICAL PROPERTIES AND PHARMACEUTICAL PREPARATIONS
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Monitoring of clinical signs in goats with transmissible spongiform encephalopathies
- Heterogeneous nutrient supply promotes maize growth and phosphorus acquisition: additive and compensatory effects of lateral roots and root hairs
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Ligand‐independent epidermal growth factor receptor hyperactivation increases sebaceous gland size and sebum secretion in mice
- The neurosteroid environment in the hippocampus exerts bi-directional effects on seizure susceptibility in mice
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Disrupted Pancreatic Exocrine Differentiation and Malabsorption in Response to Chronic Elevated Systemic Glucocorticoid
- Association of epidemiological and biochemical factors with premature graying of hair: A case–control study
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Converging physiological roles of the anthrax toxin receptors
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Extracellular Vesicles as Surrogates for Drug Metabolism and Clearance: Promise vs. Reality
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Essential resources and best practices for laboratory mouse research