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    Research 91–120 of 1000+

    1. Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes Biology of Sex Differences · 2022 · 52 citations
    2. Combinatorial Biosynthesis of Sulfated Benzenediol Lactones with a Phenolic Sulfotransferase from Fusarium graminearum PH-1 mSphere · 2020 · 22 citations
    3. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    4. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    5. Cell Polarization Defects in Early Heart Development Circulation Research · 2007 · 9 citations
    6. Advancing Design Strategy of PROTACs for Cancer Therapy MedComm · 2025 · 4 citations
    7. Evaluating the Metabolomic Profile and Anti-Pathogenic Properties of Cannabis Species Metabolites · 2024 · 9 citations
    8. Recent Advances in the Electro-Active Therapeutic Phytochemical-Based Sensors Electrochem · 2022 · 2 citations
    9. Mixed-Culture Fermentation of Coffee Pulp Induces Metabolomic Changes and Enhances Multi-Target Bioactivity Relevant to Androgenetic Alopecia International Journal of Molecular Sciences · 2026
    10. The Anti-atopic Lotions Containing Fucoidan Extracted from Ecklonia Cava Impact on Hairless Mice Atopic Dermatitis Skin 한국생물공학회 학술대회 · 2011
    11. The Influence of Allium cepa Extracts on Promotion of Hair Growth 한국생물공학회 학술대회 · 2009 · 1 citations
    12. Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita Journal of Investigative Dermatology · 2012 · 22 citations
    13. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    14. Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene Endocrine · 2011 · 8 citations
    15. Autosomal recessive hereditary hypotrichosis simplex: A case report JAAD Case Reports · 2024
    16. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    17. TRPV3 Ion Channel: From Gene to Pharmacology International Journal of Molecular Sciences · 2023 · 2 citations
    18. Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023 Irish Journal of Medical Science (1971 -) · 2024
    19. Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa EMBO molecular medicine · 2024
    20. The Role of Nrf2 in Hearing Loss Frontiers in Pharmacology · 2021 · 17 citations
    21. Research progress on the natural products in the intervention of myocardial infarction Frontiers in Pharmacology · 2024 · 9 citations
    22. Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives Fermentation · 2023
    23. Riboflavin-responsive glutaryl CoA dehydrogenase deficiency Molecular Genetics and Metabolism · 2005 · 25 citations
    24. Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients Clinical Cosmetic and Investigational Dermatology · 2025
    25. Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings Scholars Journal of Medical Case Reports · 2021
    26. Ischemic Stroke in a Young Adult Male During Finasteride Therapy Cureus · 2026
    27. Alopecia in women submitted to childhood X-ray epilation for tinea capitis treatment British Journal of Dermatology · 2010 · 7 citations
    28. The Genetics of Human Skin Disease Cold Spring Harbor Perspectives in Medicine · 2014 · 24 citations
    29. Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review Cureus · 2025
    30. Tsukushi is involved in the wound healing by regulating the expression of cytokines and growth factors Journal of Cell Communication and Signaling · 2014 · 21 citations