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Research 331–360 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A role for p75 neurotrophin receptor in the control of apoptosis‐driven hair follicle regression
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Biology and Genetics of Hair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- FOXO1, TGF-β Regulation and Wound Healing
- Learning from nudity: lessons from the nude phenotype
- Female pattern hair loss
- Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Cutaneous lupus erythematosus
- Effects of 5-alpha reductase inhibitors on erectile function, sexual desire and ejaculation
- Mechanisms of Disease: selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 as a novel treatment for the metabolic syndrome
- Pathways to inflammation: acne pathophysiology
- From neural crest cells to melanocytes: cellular plasticity during development and beyond
- The Role of Micronutrients in Alopecia Areata: A Review
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Zinc as an ambivalent but potent modulator of murine hair growth in vivo- preliminary observations
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Bacteria induce skin regeneration via IL-1β signaling
- How to diagnose a lipodystrophy syndrome
- Prolactin delays hair regrowth in mice
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16