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    Research 31–60 of 1000+

    1. The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation American Journal Of Pathology · 1999 · 166 citations
    2. Morphological Approach to Hair Disorders Journal of Investigative Dermatology Symposium Proceedings · 2003 · 38 citations
    3. A Newborn With Hair Loss Clinical pediatrics · 2013 · 1 citations
    4. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    5. Interactions of the Vitamin D Receptor with the Corepressor Hairless Journal of Biological Chemistry · 2007 · 42 citations
    6. Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm Journal of Investigative Dermatology · 2011 · 26 citations
    7. Disease causing homozygous variants in the human hairless gene International Journal of Dermatology · 2015 · 7 citations
    8. Reply Journal of Investigative Dermatology · 2000 · 2 citations
    9. Commonly associated disorders with complete scalp alopecia in early childhood: A review International journal of trichology · 2023
    10. Alopecia totalis in an infant Cosmoderma · 2023
    11. Hairless: A nuclear receptor corepressor essential for skin function Advances in developmental biology · 2006
    12. Molecular basis of congenital atrichia in humans and mice. PubMed · 1999 · 15 citations
    13. Congenital atrichia associated with nevus flammeus: A rare association Indian dermatology online journal · 2014 · 2 citations
    14. Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan Pakistan Journal of Zoology · 2020
    15. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    16. A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia Journal of Investigative Dermatology · 2002 · 26 citations
    17. Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene 2001 · 139 citations
    18. Congenital atrichia associated with situs inversus and mesocardia International journal of trichology · 2012 · 5 citations
    19. Mutation des menschlichen hairless -Gens bei Atrichia universalis Der Hautarzt · 1998 · 2 citations
    20. A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers The American Journal of Human Genetics · 1998 · 83 citations
    21. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    22. Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup> Photochemistry and photobiology · 2008 · 10 citations
    23. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    24. Genetics of Structural Hair Disorders Journal of Investigative Dermatology · 2012 · 17 citations
    25. Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases Indian Dermatology Online Journal · 2025
    26. A review of genotrichoses and hair pathology associated with inherited skin diseases British Journal of Dermatology · 2023 · 8 citations
    27. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    28. The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor Genes & Development · 2001 · 178 citations
    29. Alopecia areata in a rhesus monkey (Macaca mulatta) Journal of Medical Primatology · 2007 · 16 citations
    30. Dermatopathology and molecular genetics Journal of The American Academy of Dermatology · 2008 · 12 citations