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    Research 181–210 of 253

    1. Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure 2007 · 51 citations
    2. Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex Genome Biology · 2019 · 48 citations
    3. Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish European Journal of Cell Biology · 2005 · 47 citations
    4. Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury Cell Reports · 2023 · 46 citations
    5. Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis Proceedings of the National Academy of Sciences of the United States of America · 2013 · 44 citations
    6. Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes ˜The œAmerican journal of pathology · 2010 · 35 citations
    7. The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i> G3 Genes Genomes Genetics · 2021 · 29 citations
    8. Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals Frontiers in Zoology · 2017 · 25 citations
    9. Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages EMBO Reports · 2015 · 25 citations
    10. Mettl3-catalyzed m <sup>6</sup> A regulates histone modifier and modification expression in self-renewing somatic tissue Science Advances · 2023 · 24 citations
    11. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice PLOS genetics · 2020 · 23 citations
    12. Developmental genetics of color pattern establishment in cats Nature communications · 2021 · 20 citations
    13. 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
    14. Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development Biology Direct · 2016 · 19 citations
    15. The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity European Journal of Cell Biology · 2005 · 18 citations
    16. Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells 2019 · 17 citations
    17. Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness eLife · 2022 · 16 citations
    18. Identification of key genes induced by platelet-rich plasma in human dermal papilla cells using bioinformatics methods Molecular Medicine Reports · 2016 · 16 citations
    19. High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders Cell Death and Disease · 2022 · 15 citations
    20. Skin-type-dependent development of murine mechanosensory neurons Developmental Cell · 2023 · 13 citations
    21. Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats Journal of Investigative Dermatology Symposium Proceedings · 2005 · 13 citations
    22. A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits Genetics selection evolution · 2021 · 11 citations
    23. Mechanism of action of bolandiol (19-nortestosterone-3β,17β-diol), a unique anabolic steroid with androgenic, estrogenic, and progestational activities 2009 · 11 citations
    24. Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle Animals · 2022 · 10 citations
    25. Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken Development · 2022 · 10 citations
    26. Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review American Journal of Medical Genetics Part A · 2021 · 10 citations
    27. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    28. Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells International journal of molecular sciences · 2018 · 9 citations
    29. Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses Cancer Research Communications · 2024 · 7 citations
    30. lncRNAs UC.145 and PRKG1-AS1 Determine the Functional Output of DKK1 in Regulating the Wnt Signaling Pathway in Gastric Cancer Cancers · 2022 · 7 citations