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    Research 331–360 of 1000+

    1. A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis Mammalian genome · 2009 · 21 citations
    2. The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis Journal of Investigative Dermatology · 2012 · 11 citations
    3. Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change BMC Genomics · 2025 · 1 citations
    4. Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia DOAJ (DOAJ: Directory of Open Access Journals) · 2011 · 1 citations
    5. FGF5 is a crucial regulator of hair length in humans Proceedings of the National Academy of Sciences of the United States of America · 2014 · 136 citations
    6. Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene Science · 1998 · 412 citations
    7. Is the Loose Anagen Hair Syndrome a Keratin Disorder? Archives of Dermatology · 2002 · 84 citations
    8. CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep ˜The œFEBS journal · 2017 · 47 citations
    9. The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs BMC Genomics · 2025
    10. Influence of NUDT15 Genotyping on Dose Intensity of Thiopurine Administration and Long-Term Clinical Outcomes (Hospitalization and Surgery) Research Square (Research Square) · 2023
    11. CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen Genes · 2020 · 13 citations
    12. Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family Frontiers in genetics · 2021 · 1 citations
    13. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    14. Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population Molecular genetics and metabolism reports · 2019 · 8 citations
    15. Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits Frontiers in genetics · 2021 · 7 citations
    16. Sox13 is a novel early marker for hair follicle development Biochemical and Biophysical Research Communications · 2019 · 6 citations
    17. Keratin 79 is a PPARA target that is highly expressed by liver damage Biochemical and biophysical research communications · 2023 · 1 citations
    18. Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome Steroids · 2019 · 1 citations
    19. Cornified Epithelial Teeth of Jawless Vertebrates Contain Proteins Similar to Keratin-Associated Proteins of Mammalian Skin Appendages Journal of Developmental Biology · 2025
    20. mTOR signaling in hair follicle and hair diseases: recent progress Frontiers in medicine · 2023
    21. Supplementary Methods, Tables 1-2 and Figures from Tumor Stroma–Derived Wnt5a Induces Differentiation of Basal Cell Carcinoma of <i>Ptch</i>-Mutant Mice via CaMKII 2023
    22. Corticotropin releasing hormone and the skin Frontiers in bioscience · 2006 · 137 citations
    23. Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects Molecules · 2020 · 37 citations
    24. Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells Medical Sciences · 2017 · 37 citations
    25. Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin Frontiers in Physiology · 2021 · 18 citations
    26. Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research Animals · 2024 · 10 citations
    27. Tissue Regeneration, Stem Cells, and Wound Healing Journal of Investigative Dermatology · 2012 · 3 citations
    28. Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome Dermatopathology · 2025
    29. Junctional Epidermolysis Bullosa, Generalized Intermediate Type 2015
    30. Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients Medicina · 2025 · 1 citations