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    Research 421–450 of 1000+

    1. 905 Dysfunction of hair follicle mesenchymal progenitors is associated with age-related hair loss 2019
    2. Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep PloS one · 2017 · 25 citations
    3. Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing BMC Genomics · 2021 · 16 citations
    4. Molecular Genetics of Alopecias Current problems in dermatology · 2015 · 9 citations
    5. Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract FEBS open bio · 2021 · 3 citations
    6. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    7. [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix]. PubMed · 2008 · 2 citations
    8. Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing Molecular Genetics & Genomic Medicine · 2025
    9. Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data Archives of Dermatological Research · 2024
    10. Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease Stem cell biology and regenerative medicine · 2018
    11. Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil Research Square (Research Square) · 2022
    12. RNA sequence analysis of dermal papilla cells’ regeneration in 3D culture Journal of Cellular and Molecular Medicine · 2020 · 6 citations
    13. 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
    14. Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant PloS one · 2012 · 6 citations
    15. ATP-dependent chromatin remodeling during mammalian development Development · 2016 · 182 citations
    16. Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq) Scientific Reports · 2020 · 39 citations
    17. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes European Journal of Human Genetics · 2019 · 36 citations
    18. Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene Journal of Pediatric Endocrinology and Metabolism · 2010 · 36 citations
    19. Gene trajectory inference for single-cell data by optimal transport metrics Nature Biotechnology · 2024 · 32 citations
    20. The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women Journal of Assisted Reproduction and Genetics · 2014 · 28 citations
    21. Formation of regulator/target gene relationships during evolution Gene · 2000 · 25 citations
    22. RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens Genes & Genomics · 2022 · 17 citations
    23. Using WGCNA (weighted gene co-expression network analysis) to identify the hub genes of skin hair follicle development in fetus stage of Inner Mongolia cashmere goat PloS one · 2020 · 16 citations
    24. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    25. Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population International Journal of Dermatology · 2013 · 11 citations
    26. The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears Veterinary Dermatology · 2008 · 10 citations
    27. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    28. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    29. Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene Endocrine · 2011 · 8 citations
    30. Transcriptome analyses of reprogrammed feather / scale chimeric explants revealed co-expressed epithelial gene networks during organ specification BMC genomics · 2018 · 7 citations