Search
for

    Sort by

    Research 31–60 of 1000+

    1. Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome Clinical and Experimental Ophthalmology · 2004 · 6 citations
    2. Skin Development and Disease: A Molecular Perspective Current Issues in Molecular Biology · 2024 · 15 citations
    3. Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages Experimental Cell Research · 2014 · 14 citations
    4. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia Genes · 2024
    5. <i>WNT10A</i> , dermatology and dentistry British Journal of Dermatology · 2021 · 30 citations
    6. Trichoscopy in Hair Shaft Disorders Dermatologic Clinics · 2018 · 36 citations
    7. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    8. Polarized microscopy in genetic hair disorders: case series 2025
    9. Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia Journal of the American Academy of Dermatology · 1985 · 101 citations
    10. Genetics of Structural Hair Disorders Journal of Investigative Dermatology · 2012 · 17 citations
    11. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    12. Hair loss among a group of Egyptian children Journal of the Egyptian Women's Dermatologic Society (Print) · 2017 · 9 citations
    13. WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation Nature Communications · 2017 · 96 citations
    14. Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia The American Journal of Human Genetics · 2012 · 74 citations
    15. Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease Annals of Internal Medicine · 1971 · 32 citations
    16. Hair and Nail Relationship Skinmed · 2005 · 21 citations
    17. Dermatopathology and molecular genetics Journal of The American Academy of Dermatology · 2008 · 12 citations
    18. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    19. Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients Journal of endocrinological investigation · 2021 · 31 citations
    20. Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1 Endocrinology, diabetes & metabolism case reports · 2020 · 2 citations
    21. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    22. Keratin disorders: from gene to therapy 2011 · 109 citations
    23. Distinct tooth regeneration systems deploy a conserved battery of genes bioRxiv (Cold Spring Harbor Laboratory) · 2020
    24. Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine Journal of Personalized Medicine · 2023 · 12 citations
    25. Molecular biology of hair morphogenesis: Development and cycling Journal Of Experimental Zoology Part B: Molecular And Developmental Evolution · 2003 · 155 citations
    26. Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations Hormone research in paediatrics · 2010 · 62 citations
    27. Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor Biochemical and Biophysical Research Communications · 2020 · 4 citations
    28. Hair Loss in Children, Etiologies, and Treatment InTech eBooks · 2017
    29. Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color Journal of the American Academy of Dermatology · 2005 · 25 citations
    30. The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle 2015 · 15 citations