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    Research 451–480 of 1000+

    1. Runx Family Genes in Tissue Stem Cell Dynamics Advances in Experimental Medicine and Biology · 2017 · 6 citations
    2. Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis Cell Reports · 2025 · 5 citations
    3. Physiology of Testicular Function Andrology · 2023 · 4 citations
    4. JAK inhibition decreases the autoimmune burden in Down syndrome eLife · 2024 · 2 citations
    5. A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia 2020 · 2 citations
    6. Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese Human Genomics · 2024 · 1 citations
    7. A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome AACE Clinical Case Reports · 2015 · 1 citations
    8. Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management Russian Journal of Child Neurology · 2024
    9. Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders ACS Omega · 2023
    10. Hair & Cutaneous Development Journal of Investigative Dermatology · 2012
    11. Genetically separable determinants of hair keratin gene expression Developmental Dynamics · 2000 · 27 citations
    12. Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1 Proceedings of the National Academy of Sciences · 2000 · 380 citations
    13. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease Journal of Cell Science · 2008 · 85 citations
    14. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    15. Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype Developmental Dynamics · 2000 · 75 citations
    16. Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions Journal of Investigative Dermatology · 2006 · 81 citations
    17. In vivo function of VDR in gene expression-VDR knock-out mice 1999 · 73 citations
    18. Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse Biochemical and Biophysical Research Communications · 2002 · 35 citations
    19. Formation of regulator/target gene relationships during evolution Gene · 2000 · 25 citations
    20. Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population Gene · 2013 · 15 citations
    21. Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1 2004
    22. Vitamin D and calcium regulation of epidermal wound healing The Journal of Steroid Biochemistry and Molecular Biology · 2015 · 86 citations
    23. 1α,25(OH)2-Dihydroxyvitamin D3/VDR protects the skin from UVB-induced tumor formation by interacting with the β-catenin pathway The Journal of Steroid Biochemistry and Molecular Biology · 2012 · 45 citations
    24. Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels Kuwait Journal of Science · 2025
    25. Human Hair Keratin‐Associated Proteins (KAPs) International review of cytology · 2006 · 226 citations
    26. Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium Mechanisms of Development · 2004 · 56 citations
    27. Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis Developmental Biology · 2003 · 53 citations
    28. Dynamic expression of Runx1 in skin affects hair structure Mechanisms of Development · 2006 · 46 citations
    29. Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament Genomics · 2007 · 27 citations
    30. A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses Bone · 2014 · 12 citations