Search
for

    Sort by

    Research 931–960 of 1000+

    1. Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population Skin Health and Disease · 2025
    2. Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review Clinical Medicine Insights Case Reports · 2025
    3. Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report BMC Urology · 2025
    4. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    5. Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations Cells · 2023
    6. https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/# 2020
    7. Engineered Hair Follicle Mesenchymal Stem Cells Overexpressing Controlled-Release Insulin Reverse Hyperglycemia in Mice with Type l Diabetes Cell transplantation · 2014 · 17 citations
    8. Predictive factors for therapeutic response and cluster analysis in syndrome of undifferentiated recurrent fever (SURF) RMD Open · 2025 · 2 citations
    9. Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement Genes · 2024
    10. Melatonin promotes the development of the secondary hair follicles by regulating circMPP5 Journal of Animal Science and Biotechnology · 2023 · 1 citations
    11. Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza Scientific reports · 2020 · 8 citations
    12. SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder Cell · 2010 · 260 citations
    13. Drug Repurposing for Rare Diseases Trends in Pharmacological Sciences · 2021 · 246 citations
    14. Associations between sugar-sweetened beverages consumption, duration of physical exercise, and depressive symptoms among Tibetan university students at high altitude Frontiers in Psychology · 2024 · 2 citations
    15. Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings 1995 · 124 citations
    16. Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa Journal of Clinical Investigation · 2017 · 87 citations
    17. Exploring Acne Treatments: From Pathophysiological Mechanisms to Emerging Therapies International Journal of Molecular Sciences · 2024 · 68 citations
    18. Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review Oncotarget · 2018 · 65 citations
    19. 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
    20. Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin Nature communications · 2019 · 36 citations
    21. Hyaluronic Acid Hydrogel Incorporating Dexpanthenol-Engineered Extracellular Vesicles for Accelerated Wound Closure and Mitigated Secondary Infection Risk Pharmaceutics · 2026
    22. Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture Cell · 2018 · 249 citations
    23. Biological Function of Long Non-coding RNA (LncRNA) Xist Frontiers in Cell and Developmental Biology · 2021 · 247 citations
    24. Molecular basis of hair cell loss 2015 · 66 citations
    25. Symptomatology of Long COVID Associated with Inherited and Acquired Thrombophilic Conditions: A Systematic Review Viruses · 2025 · 1 citations
    26. Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle PloS one · 2015 · 31 citations
    27. Acute COVID-19 Syndrome Predicts Severe Long COVID-19: An Observational Study Cureus · 2022 · 5 citations
    28. Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects Frontiers in Immunology · 2026
    29. A Profuse Pipeline of Promising Options Sustainable development goals series · 2022
    30. [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis]. PubMed · 2007 · 1 citations