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Research 751–780 of 1000+
- Peptide-Based Approaches for Pain Relief and Healing in Wounds
- Treg–tissue cell interactions in repair and regeneration
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Finasteride delays atherosclerosis progression in mice and is associated with a reduction in plasma cholesterol in men
- Diphenyl cresyl phosphate [MAK Value Documentations, 2003]
- 25-Year-Old Woman With New-Onset Seizures
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- 3D spheroid culture synchronizes heterogeneous MSCs into an immunomodulatory phenotype with enhanced anti-inflammatory effects
- Antigen presenting cells in the skin of a patient with hair loss and systemic lupus erythematosus.
- Macrophages in Skin Wounds: Functions and Therapeutic Potential
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Pericyte Plasticity in the Brain
- Aggressive treatment in paediatric or young patients with drug-induced hypersensitivity syndrome (DiHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) is associated with future development of type III polyglandular autoimmune syndrome
- The Link Between Obesity and the Skin
- Exploring Platelet-Rich Plasma Therapy for Knee Osteoarthritis: An In-Depth Analysis
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Severe Acute SARS-CoV-2 Infection and Long COVID: What Do We Know So Far? New Challenges in Diagnosis and Management
- Skin Manifestations of Rheumatological Diseases
- ESCITALOPRAM
- Syphilitic alopecia: uncommon trichoscopic findings
- Multiple potential roles of thymosin β4 in the growth and development of hair follicles
- Pathologic Quiz Case: Unexplained Hair Loss—1 Boy, 2 Cats, and 1 Dog
- Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Epigenetics of Colorectal Cancer
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Peptidylarginine Deiminase Isoforms Are Differentially Expressed in the Anagen Hair Follicles and Other Human Skin Appendages
- The Potential of Ginkgo biloba as a Source of Biologically Active Compounds—A Review of the Recent Literature and Patents