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Research 871–900 of 1000+
- Targeted protein degradation of Wnt/β-catenin signaling pathway: an effective strategy for cancer therapy
- Identification of functional circRNAs regulating ovarian follicle development in goats
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Androgens in cervical cancer: Their role in epidemiology and biology
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Regulation of cashmere fineness traits by noncoding RNA in Jiangnan cashmere goats
- Keratinocyte-Expressed Podoplanin is Dispensable for Multi-Step Skin Carcinogenesis
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Methyl Jasmonate Activates the 2C Methyl-D-erithrytol 2,4-cyclodiphosphate Synthase Gene and Stimulates Tanshinone Accumulation in Salvia miltiorrhiza Solid Callus Cultures
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Prefrontal 5α-reductase 2 mediates male-specific acute stress response
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Physiology of Testicular Function
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Neutrophil extracellular traps impair regeneration
- Spatiotemporal Labeling of Melanocytes in Mice
- Molecular Engineering of Recombinant Protein Hydrogels: Programmable Design and Biomedical Applications
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Coordination of force-generating actin-based modules stabilizes and remodels membranes in vivo
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms