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    Research 151–180 of 1000+

    1. THY1-mediated mechanisms converge to drive YAP activation in skin homeostasis and repair Nature Cell Biology · 2022 · 23 citations
    2. Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene 2015 · 22 citations
    3. Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro American Journal Of Pathology · 2003 · 20 citations
    4. Nuclear Localization of STAT5A Modified with O-Linked N-Acetylglucosamine and Early Involution in the Mammary Gland of Hirosaki Hairless Rat Journal of Biological Chemistry · 2005 · 17 citations
    5. Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes Journal of child neurology · 2012 · 15 citations
    6. Impaired Keratinocyte Proliferative and Clonogenic Potential in Transgenic Mice Overexpressing 14-3-3σ in the Epidermis Journal of Investigative Dermatology · 2011 · 15 citations
    7. A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in <i>Arabidopsis</i> Plant Cell & Environment · 2022 · 14 citations
    8. PR-independent neurosteroid regulation of α2-GABA-A receptors in the hippocampus subfields Brain research · 2017 · 14 citations
    9. HR Gene Variants Identified in Mexican Patients with Alopecia Areata Current Issues in Molecular Biology · 2023 · 6 citations
    10. Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS International Journal of Endocrinology · 2021 · 6 citations
    11. Genetic Variants and Protective Immunity against SARS-CoV-2 Genes · 2022 · 5 citations
    12. The Arabidopsis Receptor-like Kinase CAP1 Promotes Shoot Growth under Ammonium Stress Biology · 2022 · 5 citations
    13. Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita Science Advances · 2025 · 3 citations
    14. Genetic association of wool quality characteristics in United States Rambouillet sheep Frontiers in genetics · 2023 · 1 citations
    15. The Rho GTPase regulator ARHGEF3 orchestrates hair placode budding by coordinating cell fate and P-cadherin patterning in mice PLoS Biology · 2026
    16. Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review Human Genomics · 2025
    17. Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development Case Reports in Genetics · 2025
    18. The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome Frontiers in cell and developmental biology · 2023
    19. Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations Cells · 2023
    20. The GPR30 agonist G-1 promotes hair growth via Wnt/Hedgehog signaling in mice Frontiers in Pharmacology · 2025
    21. Knockout of the ING5 epigenetic regulator confirms roles in stem cell maintenance and tumor suppression in vivo PLoS ONE · 2025
    22. 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
    23. Sox13 is a novel early marker for hair follicle development Biochemical and Biophysical Research Communications · 2019 · 6 citations
    24. <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development Animal Cells and Systems · 2021 · 2 citations
    25. Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet ˜The œFASEB journal · 2013 · 28 citations
    26. Role of the Wnt signaling pathway in keratoacanthoma Cancer reports · 2019 · 2 citations
    27. Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study Research Square (Research Square) · 2022
    28. Polycystic ovary syndrome: a complex condition with psychological, reproductive and metabolic manifestations that impacts on health across the lifespan BMC Medicine · 2010 · 926 citations
    29. Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival Science Translational Medicine · 2016 · 237 citations
    30. Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy Journal of Investigative Dermatology · 2003 · 52 citations