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Research 121–150 of 1000+
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Aging and Immortality: Quasi-Programmed Senescence and Its Pharmacologic Inhibition
- Transforming growth factor-β in stem cells and tissue homeostasis
- Frontal fibrosing alopecia in postmenopausal women
- Cutaneous complications of chemotherapeutic agents
- A matter of life and death: self‐renewal in stem cells
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Exosomes for repair, regeneration and rejuvenation
- Acne, the Skin Microbiome, and Antibiotic Treatment
- Frontal fibrosing alopecia versus lichen planopilaris: a clinicopathological study
- Human epithelial hair follicle stem cells and their progeny: Current state of knowledge, the widening gap in translational research and future challenges
- Biology and Genetics of Hair
- FOXO1, TGF-β Regulation and Wound Healing
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- p53 Involvement in the Control of Murine Hair Follicle Regression
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The role of lymphocytes in the development and treatment of alopecia areata
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner
- Overview of Facial Plastic Surgery and Current Developments
- Ruxolitinib for the treatment of severe alopecia areata
- Androgen Deprivation Therapy in Prostate Cancer: Focusing on Sexual Side Effects
- Hydrogen peroxide and monoethanolamine are the key causative ingredients for hair dye-induced dermatitis and hair loss
- Gender Differences in Cardiac Hypertrophy
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Newborn infant skin gene expression: Remarkable differences versus adults
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain