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    Research 271–300 of 1000+

    1. CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy Cureus · 2026
    2. Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor Biomolecules · 2023
    3. Signaling pathways in hair aging Frontiers in cell and developmental biology · 2023
    4. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    5. Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns Developmental Biology · 2017 · 33 citations
    6. 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
    7. 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation Journal of Investigative Dermatology · 2017
    8. A Case Report of Werner’s Syndrome With a Novel Mutation From India Cureus · 2020 · 4 citations
    9. Mediator1: An Important Intermediary of Vitamin D Receptor–Regulated Epidermal Function and Hair Follicle Biology Journal of Investigative Dermatology · 2012 · 5 citations
    10. Revealing novel insights on how oral supplementation with collagen peptides may prevent hair loss: Lessons from the human hair follicle organ culture Journal of functional foods · 2024
    11. Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis PloS one · 2015 · 63 citations
    12. NAD⁺ Biology in Ageing and Chronic Disease: Mechanisms and Evidence across Skin, Fertility, Osteoarthritis, Hearing and Vision Loss, Gut Health, Cardiovascular–Hepatic Metabolism, Neurological Disorders, and Muscle Annals of Clinical Endocrinology and Metabolism · 2026
    13. Deimination in epidermal barrier and hair formation Philosophical transactions - Royal Society. Biological sciences · 2023 · 2 citations
    14. Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice Immunogenetics · 2008 · 7 citations
    15. Pathogenesis and management of TRPV3-related Olmsted syndrome Frontiers in Genetics · 2024
    16. Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant PloS one · 2012 · 8 citations
    17. A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice. Proceedings of the National Academy of Sciences · 1996 · 89 citations
    18. An essential role for <i>Rxrα</i> in the development of Th2 responses European Journal of Immunology · 2005 · 50 citations
    19. Ptch2 is a Potential Regulator of Mesenchymal Stem Cells Frontiers in Physiology · 2022 · 3 citations
    20. TRP Channels in Skin Biology and Pathophysiology Pharmaceuticals · 2016 · 124 citations
    21. Hairless triggers reactivation of hair growth by promoting Wnt signaling Proceedings of the National Academy of Sciences of the United States of America · 2005 · 137 citations
    22. Keratinocyte Stem Cells: Role in Aging IntechOpen eBooks · 2022 · 1 citations
    23. Molecular Mechanisms Regulating Hair Follicle Development 2002 · 854 citations
    24. Spreading of Isolated Ptch Mutant Basal Cell Carcinoma Precursors Is Physiologically Suppressed and Counteracts Tumor Formation in Mice International journal of molecular sciences · 2020 · 1 citations
    25. Animal and in vitro Models for the Study of Hair Follicles Journal of Investigative Dermatology Symposium Proceedings · 2003 · 45 citations
    26. A Case of IFAP Syndrome with Severe Atopic Dermatitis Case reports in medicine · 2015 · 5 citations
    27. MitoQ upregulates CYP19A1 to protect dermal papilla cells from DHT-induced mitochondrial dysfunction and apoptosis in androgenetic alopecia Biochemical Pharmacology · 2026
    28. TRPV3 Ion Channel: From Gene to Pharmacology International Journal of Molecular Sciences · 2023 · 2 citations
    29. SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets Journal of the Endocrine Society · 2024
    30. Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia ˜The œAmerican journal of pathology · 2000 · 179 citations