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Research 181–210 of 1000+
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- The Role of Histone Demethylases in Disease
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- ATP-dependent chromatin remodeling during mammalian development
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Targeting the Wnt pathways for therapies
- Beyond Expectations
- Genetic Fate Mapping Using Site-Specific Recombinases
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- Polycystic ovary syndrome: An update on diagnosis and management
- The Use of Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryos during Organogenesis and Their Role in Regulating the Gene Expression of Normal and Pathological (Stem) Cells
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Transforming growth factor-β in stem cells and tissue homeostasis
- Volatile signalling by sesquiterpenes from ectomycorrhizal fungi reprogrammes root architecture
- The Harmonies Played by TGF-β in Stem Cell Biology
- Mesenchymal Stem Cells from Adipose Tissue in Clinical Applications for Dermatological Indications and Skin Aging
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Obesity and polycystic ovary syndrome
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- COVID-19 and endocrine and metabolic diseases. An updated statement from the European Society of Endocrinology
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- The regeneration blastema of lizards: an amniote model for the study of appendage replacement
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Melatonin promotes Cashmere goat (<i>Capra hircus</i>) secondary hair follicle growth: a view from integrated analysis of long non-coding and coding RNAs
- Stem cells and aberrant signaling of molecular systems in skin aging