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    Research 31–60 of 1000+

    1. Trichothiodystrophy with Dysmyelination and Central Osteosclerosis American Journal of Neuroradiology · 2010 · 16 citations
    2. Cantú syndrome with coexisting familial pituitary adenoma Endocrine · 2018 · 14 citations
    3. Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS 2026
    4. MIXED CONNECTIVE TISSUE DISEASE EVOLVING FROM THE SEQUENTIAL OVERLAP OF SYSTEMIC LUPUS ERYTHEMATOSUS, SJÖGREN’S SYNDROME, RHEUMATOID ARTHRITIS AND DERMATOMYOSITIS: A FOLLOW-UP The Journal of Rheumatology · 2025
    5. What’s New in the Histologic Evaluation of Alopecia and Hair-Related Disorders? Dermatologic Clinics · 2012 · 4 citations
    6. SINDROMA CUSHING PADA KEHAMILAN INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY · 2018 · 2 citations
    7. Hardwiring Stem Cell Communication through Tissue Structure Cell · 2016 · 82 citations
    8. Molecular Cloning and Expression Analysis of Prostaglandin E Receptor 2 Gene in Cashmere Goat (<i>Capra hircus</i>) Skin during Hair Follicle Development Animal Biotechnology · 2014 · 2 citations
    9. Developmental Mechanisms Controlling Cell Fate, Evolution of Elsevier eBooks · 2016
    10. Cosmetic Surgery Considerations in the Female Patient Oral and Maxillofacial Surgery Clinics of North America · 2007 · 4 citations
    11. Intramembrane Proteolysis of Astrotactins Journal of Biological Chemistry · 2017 · 8 citations
    12. Expression of hair-related keratins in a soft epithelium: Subpopulations of human and mouse dorsal tongue keratinocytes express keratin markers for hair-, skin- and esophageal-types of differentiation Experimental Cell Research · 1989 · 128 citations
    13. Omenn syndrome in a 10-month-old male with athymia and VACTERL association Journal of allergy and clinical Immunology. Global · 2023
    14. LHX2: a transcription factor in development, homeostasis, repair, and disease Frontiers in Cell and Developmental Biology · 2026
    15. Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan Journal of Animal Reproduciton and Biotechnology · 2024
    16. Embryonic keratinization in vertebrates in relation to land colonization Acta Zoologica · 2008 · 44 citations
    17. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    18. Hair Follicle Development in Mouse Pluripotent Stem Cell-Derived Skin Organoids Cell Reports · 2018 · 169 citations
    19. Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature Pediatric neurology · 2008 · 23 citations
    20. Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling Biology · 2026
    21. Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics iMeta · 2024
    22. On the Horizon From the ORS Journal of the American Academy of Orthopaedic Surgeons · 2010 · 11 citations
    23. Comparison between low-dose chemotherapy and surgery for the treatment of extremity-associated solitary bone lesions in children with Langerhans cell histiocytosis in South China: A case-control study Journal of bone oncology · 2018 · 2 citations
    24. Late-Onset Systemic Lupus Erythematosus Medicine · 2004 · 227 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. Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains Annals of the New York Academy of Sciences · 2025 · 4 citations
    27. Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome Orphanet Journal of Rare Diseases · 2011 · 71 citations
    28. Single-Cell Transcriptomic Identification of a Proliferative Intermediate State During Early Anagen Hair Follicle Regeneration Genes · 2026
    29. A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2 Revista Paulista de Pediatria · 2023
    30. Rare Case of Alopecia: Alopecia Neoplastica International Journal of Trichology · 2025