Search
for

    Sort by

    Research 331–360 of 595

    1. <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i> New phytologist · 2023
    2. Barbering in Laboratory Rodents: Problems and Prospects Российский физиологический журнал им  И  М  Сеченова · 2024
    3. Epimorphic regeneration in mice is p53-independent Cell Cycle · 2010 · 20 citations
    4. Roles of tumor suppressors in regulating tumor-associated inflammation Cell Death & Differentiation · 2014 · 44 citations
    5. Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia Journal of Investigative Dermatology · 2025
    6. Direct conversion of mouse and human fibroblasts to functional melanocytes by defined factors Nature Communications · 2014 · 66 citations
    7. Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities Signal Transduction and Targeted Therapy · 2022 · 318 citations
    8. Feasibility of repairing full-thickness skin defects by iPSC-derived epithelial stem cells seeded on a human acellular amniotic membrane Stem cell research & therapy · 2019 · 23 citations
    9. Promotion of homology-directed DNA repair by polyamines Nature communications · 2019 · 47 citations
    10. The role of WNT10B in physiology and disease: A 10-year update Frontiers in Cell and Developmental Biology · 2023 · 27 citations
    11. Exosomes in Aesthetic Medicine: An Overview Aesthetic Surgery Journal · 2025
    12. The Potential Role of Exosomes in Aesthetic Plastic Surgery: A Review of Current Literature Plastic and Reconstructive Surgery – Global Open · 2023
    13. Epithelial Stem Cells: Turning over New Leaves Cell · 2007 · 508 citations
    14. Knockout of the ING5 epigenetic regulator confirms roles in stem cell maintenance and tumor suppression in vivo PLoS ONE · 2025
    15. Trichotillomania in children and adolescents: Review of the literature and case report Child Psychiatry & Human Development · 1990 · 27 citations
    16. Depletion of S100A4+ stromal cells results in abnormal nipple development and nursing failure 2026
    17. Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase PLoS Genetics · 2010 · 73 citations
    18. Parents May Over-report Use of Home Safety Interventions Aap Grand Rounds · 2003
    19. Management of congenital ichthyoses: European guidelines of care, part two British Journal of Dermatology · 2018 · 66 citations
    20. Improvement of androgenic alopecia by extracellular vesicles secreted from hyaluronic acid-stimulated induced mesenchymal stem cells Stem Cell Research & Therapy · 2024
    21. Evaluation of quality of life scores and family impact scales in pediatric patients with alopecia areata: a cross‐sectional cohort study International Journal of Dermatology · 2024 · 7 citations
    22. Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study Frontiers in Immunology · 2023 · 4 citations
    23. The Use of 308-nm Excimer Laser Therapy in Alopecia Areata and Primary Cicatricial Alopecia: A Systematic Review Applied Sciences · 2026
    24. Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease Cell Reports · 2022 · 14 citations
    25. 126 cAMP response element-binding protein 1 (CREB) is a β-catenin-regulated transcription factor in squamous cell carcinoma (SCC) cells Journal of Investigative Dermatology · 2018
    26. Sp6 downregulation of follistatin gene expression in ameloblasts Journal of medical investigation · 2008 · 28 citations
    27. Heavy Metals (Cadmium, Zinc, Nickel, Chrome, Lead, and Copper) Contamination in Kohl Available in Iran’s Market 2016 · 3 citations
    28. Alopecia Areata in Children: Quality of Life for Children and Their Parents American journal of clinical medicine research · 2023
    29. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    30. What is the Rationale for Androgen Therapy for Women? Treatments in Endocrinology · 2003 · 20 citations