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    Research 391–420 of 1000+

    1. 3,4,5-Tri-O-Caffeoylquinic Acid Promoted Hair Pigmentation Through β-Catenin and Its Target Genes Frontiers in cell and developmental biology · 2020 · 13 citations
    2. A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient Journal of Dermatological Science · 2009 · 13 citations
    3. The effect of night shift work on the expression of clock genes in beard hair follicle cells Sleep medicine · 2019 · 12 citations
    4. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    5. 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
    6. Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin Skin pharmacology and physiology · 2015 · 11 citations
    7. 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
    8. Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model Tissue Engineering and Regenerative Medicine · 2024 · 9 citations
    9. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    10. The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata Medicine · 2019 · 9 citations
    11. Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India Journal of Natural Fibers · 2018 · 9 citations
    12. A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family 2018 · 9 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. Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome Reproductive Biomedicine Online · 2015 · 9 citations
    15. The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth Archives of Dermatological Research · 2013 · 9 citations
    16. Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle Scientific Reports · 2011 · 9 citations
    17. The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets? 2005 · 9 citations
    18. Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon Mammalian genome · 2004 · 8 citations
    19. Shh Gene Regulates the Proliferation and Apoptosis of Dermal Papilla Cells to Affect Its Differential Expression in Secondary Hair Follicle Growth Cycle of Cashmere Goats Animals · 2024 · 7 citations
    20. HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome Journal of the Formosan Medical Association · 2019 · 7 citations
    21. Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum Neurodegenerative Diseases · 2018 · 7 citations
    22. Disease causing homozygous variants in the human hairless gene International Journal of Dermatology · 2015 · 7 citations
    23. Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System Pharmaceutics · 2024 · 6 citations
    24. A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat Animal Biotechnology · 2023 · 6 citations
    25. HR Gene Variants Identified in Mexican Patients with Alopecia Areata Current Issues in Molecular Biology · 2023 · 6 citations
    26. CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico Anais Brasileiros de Dermatologia · 2020 · 6 citations
    27. A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients BMC Medical Genetics · 2020 · 6 citations
    28. Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study The application of clinical genetics · 2019 · 6 citations
    29. 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
    30. Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis Springer eBooks · 2010 · 6 citations