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    Research 121–150 of 1000+

    1. Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle Scientific Reports · 2011 · 9 citations
    2. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    3. Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein Scientific Reports · 2018 · 27 citations
    4. Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells Plant Physiology · 2010 · 122 citations
    5. Structure of human type II 5 alpha-reductase gene. Endocrinology · 1992 · 124 citations
    6. Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia American Journal of Human Genetics · 2005 · 195 citations
    7. Age-associated inflammation inhibits epidermal stem cell function Genes & development · 2012 · 144 citations
    8. Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1 Journal of Investigative Dermatology · 1994 · 25 citations
    9. The Genetics of Human Skin Disease Cold Spring Harbor Perspectives in Medicine · 2014 · 24 citations
    10. A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient Journal of Dermatological Science · 2009 · 13 citations
    11. 196 The endocannabinoid tone regulates human sebocyte biology Journal of Investigative Dermatology · 2016
    12. 192 MicroRNAs and their regulatory interactions in the human hair follicle Journal of Investigative Dermatology · 2016
    13. Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in the<i>Arabidopsis</i>Root The Plant Cell · 2010 · 84 citations
    14. A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice 2008 · 60 citations
    15. Single-strand DNA breaks in human hair root cells exposed to mobile phone radiation International Journal of Radiation Biology · 2012 · 37 citations
    16. Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle Frontiers in genetics · 2020 · 26 citations
    17. Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling PLOS ONE · 2012 · 9 citations
    18. CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne Postepy Dermatologii I Alergologii · 2019 · 7 citations
    19. Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD) Journal of Steroid Biochemistry · 1990 · 3 citations
    20. Role of the Wnt signaling pathway in keratoacanthoma Cancer reports · 2019 · 2 citations
    21. Role of hair as Evidence in Investigation: A Forensic Approach 2013 · 2 citations
    22. Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats Research Square (Research Square) · 2019 · 1 citations
    23. Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients OSMANGAZİ JOURNAL OF MEDICINE · 2024
    24. Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese 2022
    25. 9. Immunology and Genetics Medical & surgical dermatology · 2009
    26. Exogenous stimulation with Eclipta alba promotes hair matrix keratinocyte proliferation and downregulates TGF-β1 expression in nude mice International Journal of Molecular Medicine · 2014 · 24 citations
    27. A curated catalog of canine and equine keratin genes PLoS ONE · 2017 · 20 citations
    28. Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer Communications biology · 2020 · 113 citations
    29. Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1 The Journal of Clinical Endocrinology and Metabolism · 2001 · 93 citations
    30. Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase PLoS Genetics · 2010 · 73 citations