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    Research 421–450 of 1000+

    1. RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome The American Journal of Human Genetics · 2012 · 112 citations
    2. Hair-Cycle-Associated Remodeling of the Peptidergic Innervation of Murine Skin, and Hair Growth Modulation by Neuropeptides Journal of Investigative Dermatology · 2001 · 112 citations
    3. Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development Proceedings of the National Academy of Sciences of the United States of America · 2003 · 93 citations
    4. Towards Defining the Pathogenesis of the Hairless Phenotype Journal of Investigative Dermatology · 1998 · 86 citations
    5. Role of FGFR2-signaling in the pathogenesis of acne Dermato-endocrinology · 2009 · 63 citations
    6. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    7. Neuropeptídeos na pele Anais Brasileiros de Dermatologia · 2003 · 27 citations
    8. Evolution of Trichocyte Keratins Advances in experimental medicine and biology · 2018 · 18 citations
    9. The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle 2015 · 15 citations
    10. Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice Journal of Biological Chemistry · 2002 · 15 citations
    11. Skin tissue engineering Stembook · 2009 · 12 citations
    12. Pilot study: Autologous platelet‐rich plasma used in a topical cream for facial rejuvenation Journal of cosmetic dermatology · 2019 · 9 citations
    13. Generation and integration of hair follicle-primed spheroids in bioengineered skin constructs Biomedical Materials · 2022 · 8 citations
    14. Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease PloS one · 2019 · 5 citations
    15. Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia Children · 2023 · 4 citations
    16. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies 2022 · 2 citations
    17. Apoptosis in Hair and Skin: A Review Journal of skin and stem cell · 2019 · 2 citations
    18. Acne Syndromes and Mosaicism Biomedicines · 2021 · 1 citations
    19. Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells Pharmaceutics · 2021 · 1 citations
    20. Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins IntechOpen eBooks · 2021 · 1 citations
    21. Current Genetics in Hair Diseases InTech eBooks · 2013 · 1 citations
    22. Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia Our Dermatology Online · 2025
    23. Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome Animal genetics · 2024
    24. EBS in Children with De Novo Pathogenic Variants Disturbing Krt14 International journal of molecular sciences · 2024
    25. The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway Cells · 2024
    26. Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report Clinical, cosmetic and investigational dermatology · 2024
    27. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
    28. Cardiovascular risk in patients with selected cutaneous diseases Journal of Education, Health and Sport · 2022
    29. ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer 2013 · 224 citations
    30. Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment GenomeBiology.com · 2015 · 153 citations