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Research 901–930 of 1000+
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Store-operated calcium channels in skin
- Frizzled Receptors in Development and Disease
- Subcellular localization of the five members of the human steroid 5α-reductase family
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Arabidopsis PCaP2 Functions as a Linker Between ABA and SA Signals in Plant Water Deficit Tolerance
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
- Proteome Analysis of Alpine Merino Sheep Skin Reveals New Insights into the Mechanisms Involved in Regulating Wool Fiber Diameter
- Advancing Aesthetic Medicine Through Exosome-Based Regenerative Therapies with Dr. Face Innovations: Molecular Mechanisms, Nanotechnology Integration, and Data-Driven Insights
- Macrophage-Derived Extracellular Vesicle Promotes Hair Growth
- Lipid signaling in keratinocytes: Lipin-1 plays a PArt
- Scientific opinion on the tolerable upper intake level for selenium
- Sex Differences in Animal Models of Sodium-Valproate-Induced Autism in Postnatal BALB/c Mice: Whole-Brain Histoarchitecture and 5-HT2A Receptor Biomarker Evidence
- Reductive Stress Selectively Disrupts Collagen Homeostasis and Modifies Growth Factor-independent Signaling Through the MAPK/Akt Pathway in Human Dermal Fibroblasts
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Changes in the proteomic profile of adipose tissue-derived mesenchymal stem cells during passages
- Extremely Low-Frequency Electromagnetic Fields Increase Cytokines in Human Hair Follicles through Wnt/β-Catenin Signaling
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Lambertianic Acid from Platycladus orientalis Inhibits Muscle Atrophy in Dexamethasone-Induced C2C12 Muscle Atrophy Cells
- In Vitro Stability and Preclinical Safety Evaluation of High-Dose Intravitreal Topotecan in Rabbits: Impact of Dose and Concentration
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Catecholaminergic neurons boost fibroblast osteogenic activity in keloid