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    Research 811–840 of 1000+

    1. ANDROGEN AND CORTISOL SECRETING ADRENOCORTICAL ONCOCYTOMA WITTH UNCERTAIN MALIGNANT POTENTIAL Journal of the ASEAN Federation of Endocrine Societies · 2019
    2. POOR WELFARE DUE TO A RARE FUNGAL SKIN DISEASE Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) · 2018
    3. To σύνδρομο της δερματίτιδας από λείξη των άκρων στο σκύλο Journal of the Hellenic Veterinary Medical Society · 2017
    4. A rash diagnosis The Medical Journal of Australia · 2017
    5. A case report and brief literature review of Klippel-Trénaunay syndrome Research and reports in neonatology · 2012
    6. P‐51 
Drug‐induced erythema multiforme or drug‐induced pemphigus foliaceus: a case report Veterinary Dermatology · 2004
    7. Androgenetic Alopecia: How It Happens Hair transplant forum international · 2015
    8. Involvement of Follicular Stem Cells in Forming Not Only the Follicle but Also the Epidermis Cell · 2000 · 1010 citations
    9. Mesenchymal Stem Cell Secretome: Toward Cell-Free Therapeutic Strategies in Regenerative Medicine International Journal of Molecular Sciences · 2017 · 773 citations
    10. Pre-Clinical Cell-Based Therapy for Limbal Stem Cell Deficiency Journal of functional biomaterials · 2015 · 28 citations
    11. Ptosis in childhood Medicine · 2018 · 15 citations
    12. Breast cancer resistance protein identifies clonogenic keratinocytes in human interfollicular epidermis Stem Cell Research & Therapy · 2015 · 14 citations
    13. The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus PLoS ONE · 2019 · 9 citations
    14. The Potential Reversible Transition between Stem Cells and Transient-Amplifying Cells: The Limbal Epithelial Stem Cell Perspective Cells · 2024 · 1 citations
    15. Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses PNAS Nexus · 2025
    16. Ocular manifestations in a case of Kallmann syndrome – An interesting case report on isolated gonadotropin-releasing hormone deficiency Indian Journal of Ophthalmology - Case Reports · 2023
    17. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria Journal of Investigative Dermatology · 2013 · 99 citations
    18. Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse Journal of Investigative Dermatology · 2009 · 92 citations
    19. Growth of secondary hair follicles of the Cashmere goat in vitro and their response to prolactin and melatonin. PubMed · 1994 · 56 citations
    20. Hyperaldosteronism and Hyperprogesteronism in a Cat Journal of Feline Medicine and Surgery · 2009 · 55 citations
    21. Regeneration Genetics Annual Review of Genetics · 2017 · 39 citations
    22. Ichthyosis with confetti: clinics, molecular genetics and management Orphanet Journal of Rare Diseases · 2015 · 36 citations
    23. Cidea Control of Lipid Storage and Secretion in Mouse and Human Sebaceous Glands Molecular and Cellular Biology · 2014 · 36 citations
    24. Androgenetic alopecia: new insights into the pathogenesis and mechanism of hair loss F1000Research · 2015 · 33 citations
    25. Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene Journal of Veterinary Internal Medicine · 2009 · 30 citations
    26. Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding Seminars in Cell & Developmental Biology · 2019 · 28 citations
    27. Dupilumab side effect in a patient with atopic dermatitis: a case report study Biologics · 2019 · 25 citations
    28. Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles Development · 2018 · 24 citations
    29. Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets Arquivos Brasileiros de Endocrinologia & Metabologia · 2008 · 24 citations
    30. Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma JAAD case reports · 2017 · 23 citations