Search
for

    Sort by

    Research 271–300 of 494

    1. Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle Frontiers in genetics · 2020 · 26 citations
    2. Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs Chemico-Biological Interactions · 1998 · 26 citations
    3. The Molecular Basis of Androgen Insensitivity Hormone Research in Paediatrics · 2000 · 25 citations
    4. Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome Genes · 2019 · 20 citations
    5. Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats Asian-Australasian Journal of Animal Sciences · 2007 · 20 citations
    6. A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation International Journal of Biological Markers · 2014 · 16 citations
    7. The genetics of alopecia areata Dermatologic Therapy · 2001 · 16 citations
    8. The Effect of Parathyroid Hormones on Hair Follicle Physiology: Implications for Treatment of Chemotherapy-Induced Alopecia Skin Pharmacology and Physiology · 2015 · 15 citations
    9. Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women Reproduction, Fertility and Development · 2010 · 15 citations
    10. Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment Scientific Reports · 2024 · 13 citations
    11. Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle Histochemistry and Cell Biology · 2021 · 13 citations
    12. Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease Translational Psychiatry · 2021 · 12 citations
    13. Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study PLoS ONE · 2019 · 12 citations
    14. MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia BMC Medical Genetics · 2019 · 12 citations
    15. Fibrous Papule of the Face, Similar to Tuberous Sclerosis Complex-Associated Angiofibroma, Shows Activation of the Mammalian Target of Rapamycin Pathway: Evidence for a Novel Therapeutic Strategy? PLoS ONE · 2014 · 12 citations
    16. Polymorphisms in androgen and estrogen receptor genes: effects on male aging Experimental Gerontology · 2004 · 12 citations
    17. The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris Advances in Dermatology and Allergology · 2020 · 10 citations
    18. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions Human Genetics · 2019 · 10 citations
    19. STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone Cell calcium · 2019 · 9 citations
    20. Physiological Doses of Red Light Induce IL‐4 Release in Cocultures between Human Keratinocytes and Immune Cells Photochemistry and Photobiology · 2017 · 9 citations
    21. Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population PLOS ONE · 2013 · 9 citations
    22. Lentiginosis within plaques of linear atrophoderma of Moulin: a twin-spotting phenomenon? British Journal of Dermatology · 2010 · 9 citations
    23. No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia British Journal of Dermatology · 2013 · 7 citations
    24. Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer Medical Oncology · 2013 · 6 citations
    25. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    26. Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment 2015 · 4 citations
    27. SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection Frontiers in Bioscience-Scholar · 2024 · 3 citations
    28. Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia PLOS ONE · 2019 · 3 citations
    29. 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
    30. Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2024 · 2 citations