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    Research 931–960 of 1000+

    1. Preliminary study on microR-148a and microR-10a in dermal papilla cells of Hu sheep BMC Genetics · 2019 · 28 citations
    2. Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep PloS one · 2017 · 25 citations
    3. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report BMC Medical Genetics · 2017 · 23 citations
    4. Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ iScience · 2020 · 22 citations
    5. Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans Journal of Interferon & Cytokine Research · 2014 · 22 citations
    6. Developmental genetics of color pattern establishment in cats Nature communications · 2021 · 20 citations
    7. Spatial Distribution and Functional Impact of Human Scalp Hair Follicle Microbiota Journal of Investigative Dermatology · 2023 · 19 citations
    8. The circular RNA circNlgnmediates doxorubicin-inducedcardiac remodeling and fibrosis Molecular therapy. Nucleic acids · 2022 · 19 citations
    9. A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report BMC dermatology · 2018 · 18 citations
    10. Alterations of gut microbiota composition in post-finasteride patients: a pilot study Journal of Endocrinological Investigation · 2020 · 17 citations
    11. Cellular heterogeneity and microenvironmental control of skin cancer Journal of Internal Medicine · 2020 · 16 citations
    12. Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction International Journal of Molecular Sciences · 2015 · 16 citations
    13. Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica 2010 · 16 citations
    14. Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat Animals · 2024 · 15 citations
    15. Screening of microRNA and mRNA related to secondary hair follicle morphogenesis and development and functional analysis in cashmere goats Functional & Integrative Genomics · 2022 · 14 citations
    16. Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats BMC genomics · 2020 · 14 citations
    17. Ranitidine and finasteride inhibit the synthesis and release of trimethylamine N-oxide and mitigates its cardiovascular and renal damage through modulating gut microbiota International Journal of Biological Sciences · 2020 · 14 citations
    18. The first case report of kerion-type scalp mycosis caused by Aspergillus protuberus BMC infectious diseases · 2019 · 14 citations
    19. Application of Cell-Derived Extracellular Vesicles and Engineered Nanovesicles for Hair Growth: From Mechanisms to Therapeutics Frontiers in cell and developmental biology · 2022 · 13 citations
    20. Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells Stem Cell Research & Therapy · 2020 · 13 citations
    21. Let-7b promotes alpaca hair growth via transcriptional repression of TGFβR I Gene · 2015 · 13 citations
    22. Effect of Sun exposure-induced ferroptosis mechanisms on pathology and potential biological processes of primary melanoma by microarray data analysis Frontiers in Genetics · 2022 · 12 citations
    23. Generation of VEGF knock-in Cashmere goat via the CRISPR/Cas9 system International Journal of Biological Sciences · 2021 · 12 citations
    24. Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers JBMR plus · 2021 · 11 citations
    25. Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome British Journal of Dermatology · 2021 · 11 citations
    26. Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women Bioscience Reports · 2019 · 11 citations
    27. Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype Journal of Investigative Dermatology · 2007 · 11 citations
    28. Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population Journal of Ovarian Research · 2014 · 10 citations
    29. Semidominant Inheritance in Epidermolytic Ichthyosis Journal of Investigative Dermatology · 2013 · 10 citations
    30. Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>) Veterinary pathology · 2010 · 10 citations