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    Research 151–180 of 1000+

    1. Itchy Black Hair Bristles on Back International journal of trichology · 2012 · 7 citations
    2. INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS 2008
    3. Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia Pediatria i Medycyna Rodzinna · 2025 · 1 citations
    4. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    5. Follicular dysplasia in two cows Veterinary Dermatology · 1999 · 10 citations
    6. Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions Journal of cutaneous pathology · 2012 · 7 citations
    7. Clinical Snippets Journal of Investigative Dermatology · 2003
    8. Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia American Journal of Human Genetics · 2007 · 109 citations
    9. Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements Journal of Human Genetics · 2016 · 30 citations
    10. Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants 2021 · 6 citations
    11. Advances in the genetic understanding of hypohidrotic ectodermal dysplasia Expert opinion on orphan drugs · 2017 · 1 citations
    12. Alopecia Areata with Renal Dysgenesis International Journal of Trichology · 2023
    13. Generalized Congenital Hypotrichosis in a Female Rottweiler Veterinary Dermatology · 1993 · 6 citations
    14. Spontaneous Squamous Cell Carcinoma Induced by the Somatic Inactivation of <i>Retinoblastoma</i> and <i>Trp53</i> Tumor Suppressors Cancer Research · 2008 · 64 citations
    15. Frizzled Receptors in Development and Disease 2016 · 114 citations
    16. Footprints of the EADV: a meeting report from the 17th Congress of the European Academy of Dermatology and Venereology British Journal of Dermatology · 2009 · 4 citations
    17. Developing Optical Biometrics Using Optical Coherence Tomography for Medical Screening and Diagnosis 2018
    18. A Very Unusual Cause of Diarrhea in a 60-Year-Old Man The American Journal of Gastroenterology · 2013
    19. Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis Tissue Antigens · 2002 · 86 citations
    20. Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia Journal of the American Academy of Dermatology · 1994 · 32 citations
    21. Skin Development and Disease: A Molecular Perspective Current Issues in Molecular Biology · 2024 · 15 citations
    22. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study Arquivos Brasileiros de Oftalmologia · 2017 · 5 citations
    23. Current Status of the Applications of Conditioned Media Derived from Mesenchymal Stem Cells for Regenerative Medicine Physiological Research · 2023 · 3 citations
    24. Dysfunction of keratinocyte adhesion Experimental Dermatology · 2004 · 2 citations
    25. Index Harper's Textbook of Pediatric Dermatology · 2019
    26. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study 2018
    27. Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency Molecular and Cellular Biology · 2004 · 75 citations
    28. A second <i>KRT</i>71 allele in curly coated dogs Animal Genetics · 2018 · 13 citations
    29. Minoxidil Cannot Be Used To Target Lysyl Hydroxylases during Postnatal Mouse Lung Development: A Cautionary Note Journal of Pharmacology and Experimental Therapeutics · 2020 · 2 citations
    30. Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners. American Journal of Medical Genetics Part A · 1999