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Research 871–900 of 1000+
- SnapshotDx Quiz: May 2022
- Polycystic ovary syndrome: a common reproductive syndrome with long-term metabolic consequences
- The Dual Nature of Cellular Senescence: From Aging Signature to Regenerative Catalyst
- Alternative androgen pathways
- The Possible Role of Antibodies in Alopecia: A Narrative Review
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Importancia de la pseudopelada de Brocq en la práctica de la medicina estética capilar
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- 76708 Risk of Developing Scarring and Non-Scarring Alopecia with GLP-1 and GLP-1/GIP Agonist Utilization
- Trichotillomania and Trichophagia: Modern Diagnostic and Therapeutic Methods
- Recommendations from the 2023 international evidence-based guideline for the assessment and management of polycystic ovary syndrome
- Botulinum Toxins in Medical and Cosmetic Dermatology
- ATP-dependent chromatin remodeling during mammalian development
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Lysophospholipid Mediators in Health and Disease
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Chronic graft versus host disease and skin
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Runx Family Genes in Tissue Stem Cell Dynamics
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy