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Research 211–240 of 1000+
- ATP-dependent chromatin remodeling during mammalian development
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- Differential Expression of Fibromodulin, a Transforming Growth Factor-β Modulator, in Fetal Skin Development and Scarless Repair
- Anthracycline analogs The past, present, and future
- Pharmacophore Modeling and Three Dimensional Database Searching for Drug Design Using Catalyst: Recent Advances
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Probiotic Bacteria Induce a ‘Glow of Health’
- Extraskeletal actions of vitamin D
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- MicroRNA-214 controls skin and hair follicle development by modulating the activity of the Wnt pathway
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Human Epidermal Neural Crest Stem Cells (hEPI-NCSC)—Characterization and Directed Differentiation into Osteocytes and Melanocytes
- Learning from nudity: lessons from the nude phenotype
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Applications of Mesenchymal Stem Cells in Skin Regeneration and Rejuvenation
- Stem cell quiescence acts as a tumour suppressor in squamous tumours
- Systematic Review of Platelet-Rich Plasma Use in Androgenetic Alopecia Compared with Minoxidil®, Finasteride®, and Adult Stem Cell-Based Therapy
- Induced Pluripotent Stem Cells from Human Hair Follicle Mesenchymal Stem Cells
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Small molecules and small molecule drugs in regenerative medicine
- Stem cell-derived motor neurons from spinal and bulbar muscular atrophy patients
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?