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    Research 211–240 of 295

    1. PA33 When bones speak through nails: insights from a paediatric case series British Journal of Dermatology · 2025
    2. The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus PLoS ONE · 2019 · 9 citations
    3. A Case of Onycholemmal Carcinoma in a 77-Year-Old Man American Journal of Dermatopathology · 2016 · 7 citations
    4. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    5. Do Changes in Chromosomes Cause Aging? Cell · 1996 · 50 citations
    6. Systemic Lupus Erythematosus With Acute Inflammatory Demyelinating Polyneuropathy: A Case Report and Review of the Literature Journal of Clinical Medicine Research · 2016 · 18 citations
    7. Chilblains in Turkey: a case-control study Anais Brasileiros de Dermatologia · 2014 · 14 citations
    8. Adult Kawasaki's disease with myocarditis, splenomegaly, and highly elevated serum ferritin levels Heart & Lung · 2009 · 13 citations
    9. Localised Skin Hyperpigmentation as a Presenting Symptom of Vitamin B12 Deficiency Complicating Chronic Atrophic Gastritis Sultan Qaboos University medical journal · 2015 · 5 citations
    10. The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin International journal of molecular sciences · 2023 · 1 citations
    11. Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways Preprints.org · 2025
    12. Fibroblast state switching orchestrates dermal maturation and wound healing Molecular Systems Biology · 2018 · 126 citations
    13. RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome The American Journal of Human Genetics · 2012 · 112 citations
    14. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis American journal of human genetics · 2019 · 53 citations
    15. The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects Developmental Dynamics · 2006 · 49 citations
    16. A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus Frontiers in Cell and Developmental Biology · 2021 · 42 citations
    17. Myotonic Dystrophy—A Progeroid Disease? Frontiers in Neurology · 2018 · 41 citations
    18. Palatogenesis and cutaneous repair: A two‐headed coin Developmental Dynamics · 2014 · 20 citations
    19. Wnt/β-Catenin Signaling during Cardiac Development and Repair Journal of Cardiovascular Development and Disease · 2014 · 9 citations
    20. Monkeypox: A Histopathological and Transmission Electron Microscopy Study Microorganisms · 2023 · 5 citations
    21. Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation Development · 2025 · 2 citations
    22. The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal Biomedicines · 2022 · 1 citations
    23. Cutaneous manifestations associated with substance use disorders JAAD reviews. · 2025
    24. Glucocorticoid-Induced Side Effects Cause Oral Lesions in Systemic Lupus Erythematosus: A Case Report International Medical Case Reports Journal · 2024
    25. Acute severe hypokalemia caused by treatment of tongue squamous cell carcinoma with docetaxel and cisplatin: A case report World Journal of Clinical Oncology · 2024
    26. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    27. Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path? Stem Cells Translational Medicine · 2017 · 32 citations
    28. Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway ˜The œAmerican journal of pathology · 2009 · 137 citations
    29. Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations 2009 · 115 citations
    30. Hox genes in development and beyond Development · 2023 · 83 citations