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Research 361–390 of 1000+
- The molecular basis of human keratin disorders
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Emerging roles of Sox6 in the renal and cardiovascular system
- Transposon control as a checkpoint for tissue regeneration
- Molecular characterization of GhPLDα1 and its relationship with secondary cell wall thickening in cotton fibers
- Spatial and single-cell transcriptomics unravel the complex interplay between the body and medical implants
- Semidominant Inheritance in Epidermolytic Ichthyosis
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- Role of EZH2 in Uterine Gland Development
- Humic acids as drivers of plant growth: regulating root development and photobiology through redox modulation
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Prediction and Demonstration of Retinoic Acid Receptor Agonist Ch55 as an Antifibrotic Agent in the Dermis
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- TRPV3 Ion Channel: From Gene to Pharmacology
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Platelet-Rich Plasma in Dermatology: New Insights on the Cellular Mechanism of Skin Repair and Regeneration
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- An ERK-dependent molecular switch antagonizes fibrosis and promotes regeneration in spiny mice ( <i>Acomys</i> )
- ILC3s as central regulators of mucosal homeostasis and disease pathogenesis (Review)
- Extra-nasal odorant receptors: molecular mechanisms and therapeutic implications
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerative Healing
- The citrullinating enzyme PADI4 governs progenitor cell proliferation and translation in developing hair follicles