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    Research 511–540 of 1000+

    1. Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome Fertility and Sterility · 2003 · 48 citations
    2. Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets. PubMed · 2016 · 39 citations
    3. Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2 Clinical Therapeutics · 2021 · 22 citations
    4. Transcriptional profiling of putative human epithelial stem cells BMC Genomics · 2008 · 16 citations
    5. Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis 2022 · 6 citations
    6. Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome 2022 · 3 citations
    7. Abstracts Experimental Dermatology · 2018 · 3 citations
    8. Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek Genes · 2022 · 2 citations
    9. A Rare Case of Cutis Verticis Gyrata with Underlying Cerebriform Intradermal Nevus Cureus · 2019 · 2 citations
    10. The genetics of autism and steroid-related traits in prenatal and postnatal life Frontiers in Endocrinology · 2023 · 1 citations
    11. Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family Frontiers in genetics · 2021 · 1 citations
    12. Acne-Associated Syndromes InTech eBooks · 2017 · 1 citations
    13. Extra-nasal odorant receptors: molecular mechanisms and therapeutic implications Frontiers in Physiology · 2026
    14. Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy Therapeutics · 2026
    15. Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy Clinical Case Reports · 2024
    16. Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings International journal of contemporary pediatrics · 2020
    17. Genetics and Pathophysiology of Congenital Adrenal Hyperplasia Contemporary Endocrinology · 2017
    18. Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation Hormones · 2016
    19. This Month in the Journal The American Journal of Human Genetics · 2005
    20. Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways Preprints.org · 2025
    21. Ectopic olfactory receptors in human: New therapeutic possibilities Authorea (Authorea) · 2020
    22. The complex relationship between TFEB transcription factor phosphorylation and subcellular localization EMBO journal · 2018 · 344 citations
    23. ATP-dependent chromatin remodeling during mammalian development Development · 2016 · 182 citations
    24. FGF Family: From Drug Development to Clinical Application International Journal of Molecular Sciences · 2018 · 103 citations
    25. A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice. Proceedings of the National Academy of Sciences · 1996 · 89 citations
    26. A complete guide to human microbiomes: Body niches, transmission, development, dysbiosis, and restoration Frontiers in Systems Biology · 2022 · 72 citations
    27. Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep PloS one · 2013 · 55 citations
    28. Therapeutic Potential of Brassinosteroids in Biomedical and Clinical Research Biomolecules · 2020 · 29 citations
    29. Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases Molecular Neurodegeneration · 2024 · 26 citations
    30. Myc and Fgf Are Required for Zebrafish Neuromast Hair Cell Regeneration PloS one · 2016 · 21 citations