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    Research 811–840 of 1000+

    1. Inflammation in androgenetic alopecia and hair loss: linking neurosciences-endocrinology-dermatology Hair transplant forum international · 2012 · 1 citations
    2. Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia Journal of Investigative Dermatology · 2025
    3. Advances in the human skin microbiota and its roles in cutaneous diseases Microbial Cell Factories · 2022 · 100 citations
    4. The role of the microbiome in scalp hair follicle biology and disease Experimental Dermatology · 2019 · 73 citations
    5. Generalized atrophic benign epidermolysis bullosa. PubMed · 1997 · 51 citations
    6. Regulatory pathway analysis of coat color genes in Mongolian horses Hereditas · 2017 · 14 citations
    7. Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats Journal of Investigative Dermatology Symposium Proceedings · 2005 · 13 citations
    8. A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family 2018 · 9 citations
    9. miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway Animals · 2025
    10. Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits International journal of molecular sciences · 2024
    11. <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i> New phytologist · 2023
    12. 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達 Institutional Repositories DataBase (IRDB) · 2022
    13. Does Vitamin D play a role on Msx1 homeoprotein expression involving an endogenous antisense mRNA?*1 2004
    14. The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis PLoS Genetics · 2012 · 99 citations
    15. Chronic overlapping pain conditions and nociplastic pain Human Genetics and Genomics Advances · 2024 · 16 citations
    16. Characterisation of Four New Genes in the Ovine KAP19 Family International Journal of Molecular Sciences · 2025
    17. Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study Medicine · 2024
    18. Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans American journal of human genetics · 2009 · 234 citations
    19. GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride Neuropsychopharmacology · 2005 · 134 citations
    20. Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome American journal of human genetics · 2016 · 119 citations
    21. Keratin disorders: from gene to therapy 2011 · 109 citations
    22. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 Mammalian genome · 2010 · 75 citations
    23. Plasticity and Cytokinetic Dynamics of the Hair Follicle Mesenchyme During the Hair Growth Cycle: Implications for Growth Control and Hair Follicle Transformations 2003 · 54 citations
    24. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    25. Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages Human Molecular Genetics · 2018 · 25 citations
    26. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    27. New-Generation Therapies for the Treatment of Hair Loss in Men Dermatologic Clinics · 2017 · 15 citations
    28. A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient Journal of Dermatological Science · 2009 · 13 citations
    29. A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype ˜The œAmerican journal of pathology · 2014 · 11 citations
    30. Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles Animals · 2023 · 10 citations