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    Research 391–420 of 1000+

    1. A Simple Method to Extract DNA from Hair Shafts Using Enzymatic Laundry Powder PLoS ONE · 2013 · 8 citations
    2. Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study Immunological Investigations · 2020 · 7 citations
    3. Interaction between estrogens and androgen receptor genes microsatellites, prostate-specific antigen and androgen receptor expressions in breast cancer Neoplasma · 2010 · 6 citations
    4. Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele Journal of the European Academy of Dermatology and Venereology · 2009 · 6 citations
    5. Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin Archives of Dermatological Research · 2019 · 5 citations
    6. Genetic correlation analysis does not associate male pattern baldness with COVID-19 Journal of The American Academy of Dermatology · 2021 · 4 citations
    7. Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels PloS one · 2018 · 4 citations
    8. SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels Meta Gene · 2018 · 3 citations
    9. Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population Postępy Dermatologii i Alergologii · 2018 · 3 citations
    10. Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium AFRICAN JOURNAL OF BIOTECHNOLOGY · 2011 · 2 citations
    11. Growth of the Mouse Coat VII. Hair Cycles and Sebaceous Glands in Homozygous and Heterozygous Naked Mice Australian Journal of Biological Sciences · 1960 · 2 citations
    12. 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells Journal of Investigative Dermatology · 2019 · 1 citations
    13. Global Landscapes of Human Phenotypic Variation in Inherited Traits Evolutionary studies · 2017 · 1 citations
    14. Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata The Annals of Clinical and Analytical Medicine · 2017 · 1 citations
    15. The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study Egyptian Journal of Medical Human Genetics · 2024
    16. The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study Research Square (Research Square) · 2023
    17. Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study Research Square (Research Square) · 2022
    18. 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy Journal of Investigative Dermatology · 2019
    19. 316 Specialized ribosomes in human dermal fibroblast senescence Journal of Investigative Dermatology · 2019
    20. 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients Journal of Investigative Dermatology · 2019
    21. 643 Male pattern baldness and risk of incident skin cancer in a cohort of men Journal of Investigative Dermatology · 2016
    22. Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes Jurnal Natural (Faculty of Mathematics and Natural Science, Syiah Kuala University) · 2010
    23. 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients Journal of The American Academy of Dermatology · 2020
    24. Anti-TNF antibody-induced psoriasiform skin lesions in patients with inflammatory bowel disease are characterised by interferon-γ-expressing Th1 cells and IL-17A/IL-22-expressing Th17 cells and respond to anti-IL-12/IL-23 antibody treatment Gut · 2013 · 278 citations
    25. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex Nature · 2010 · 199 citations
    26. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    27. The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology Best Practice & Research in Clinical Obstetrics & Gynaecology · 2004 · 131 citations
    28. THE PATHOGENESIS OF ALOPECIA AREATA Dermatologic Clinics · 1996 · 89 citations
    29. Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations Hormone research in paediatrics · 2010 · 62 citations
    30. De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle Journal of Investigative Dermatology · 2010 · 41 citations