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    Research 271–300 of 1000+

    1. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria Journal of Investigative Dermatology · 2013 · 99 citations
    2. Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds BMC Veterinary Research · 2021 · 55 citations
    3. Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan Genes · 2016 · 9 citations
    4. A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice DNA Research · 2004 · 6 citations
    5. Exome analysis for Cronkhite-Canada syndrome: A case report World Journal of Clinical Cases · 2022 · 2 citations
    6. Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient International journal of dermatology and venereology · 2022
    7. Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review Oncotarget · 2018 · 65 citations
    8. Hair Keratins and Hair Follicle–Specific Epithelial Keratins Methods in cell biology · 2004 · 31 citations
    9. The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome Frontiers in Endocrinology · 2023
    10. Regulation of Involucrin Gene Expression Journal of Investigative Dermatology · 2004 · 138 citations
    11. 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
    12. Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes Journal of Investigative Dermatology · 2004 · 49 citations
    13. Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits International Journal of Genomics · 2020 · 46 citations
    14. A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue Journal of Investigative Dermatology · 2004 · 31 citations
    15. 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
    16. Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation 2002 · 25 citations
    17. Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes Hormones · 2017 · 15 citations
    18. An important role of podoplanin in hair follicle growth PLoS ONE · 2019 · 13 citations
    19. Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle Animals · 2022 · 10 citations
    20. Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken Development · 2022 · 10 citations
    21. Recent Advances in Genome-Editing Technology with CRISPR/Cas9 Variants and Stimuli-Responsive Targeting Approaches within Tumor Cells: A Future Perspective of Cancer Management International Journal of Molecular Sciences · 2023 · 1 citations
    22. Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>) Animal Advances · 2026
    23. Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review Human Genomics · 2025
    24. Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics iMeta · 2024
    25. A comprehensive atlas of endogenous peptides in maize iMeta · 2024
    26. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia Genes · 2024
    27. Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome The Application of Clinical Genetics · 2022 · 2 citations
    28. A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers The American Journal of Human Genetics · 1998 · 83 citations
    29. Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2) Journal of Investigative Dermatology · 2003 · 22 citations
    30. A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds Scientific reports · 2017 · 17 citations