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    Research 511–540 of 1000+

    1. A symphony of signals: the intricate role of lncRNAs in dermatological disorders Clinical and Experimental Medicine · 2025 · 1 citations
    2. The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity Frontiers in Microbiology · 2019 · 91 citations
    3. Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter Animals · 2019 · 25 citations
    4. Expression of Neutrophil Gelatinase-Associated Lipocalin in Calcium-Induced Keratinocyte Differentiation Journal of Korean Medical Science · 2008 · 20 citations
    5. Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep Animals · 2024 · 4 citations
    6. A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle Genes · 2021 · 2 citations
    7. p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials Cell Death Discovery · 2026
    8. Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits Animals · 2025
    9. Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts Cells · 2025
    10. How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns Pigment Cell & Melanoma Research · 2013
    11. A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds Scientific reports · 2017 · 17 citations
    12. The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted Current Biology · 1998 · 153 citations
    13. BMI1 is required for melanocyte stem cell maintenance and hair pigmentation Pigment Cell & Melanoma Research · 2023 · 4 citations
    14. Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Frontiers in Genetics · 2023 · 1 citations
    15. A Receptor-Like Kinase Mediates Ammonium Homeostasis and Is Important for the Polar Growth of Root Hairs in<i>Arabidopsis</i> ˜The œPlant cell · 2014 · 107 citations
    16. A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA The Journal of Clinical Endocrinology & Metabolism · 2022 · 4 citations
    17. Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion Journal of Clinical Medicine · 2021 · 4 citations
    18. Promoter Methylation Changes in KRT17: A Novel Epigenetic Marker for Wool Production in Angora Rabbit International journal of molecular sciences · 2022 · 2 citations
    19. The Role of Histone Demethylases in Disease Springer eBooks · 2011 · 1 citations
    20. Down‐regulation of Shh in the hair follicles of mice during chemotherapy‐induced hair loss is mediated by the JAK / STAT1 signaling pathway FEBS Open Bio · 2025
    21. RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters BMC Genomics · 2025
    22. Discovery of HAP Stem Cells Methods in molecular biology · 2016
    23. Identification of functional circRNAs regulating ovarian follicle development in goats BMC Genomics · 2024 · 8 citations
    24. Sox2-positive dermal papilla cells specify hair follicle type in mammalian epidermis Development · 2009 · 338 citations
    25. SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin Journal of Investigative Dermatology · 2018 · 225 citations
    26. Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart Journal of Investigative Dermatology · 2004 · 22 citations
    27. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    28. Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss EBioMedicine · 2020 · 19 citations
    29. Comparative transcriptomic analysis of human mesenchymal stem cells derived from dental pulp and adipose tissues Journal of Stem Cells & Regenerative Medicine · 2019 · 8 citations
    30. Dermal lymphatic dilation in a mouse model of alopecia areata Experimental and molecular pathology · 2016 · 5 citations