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    Research 151–180 of 1000+

    1. Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms Genome Biology and Evolution · 2014 · 72 citations
    2. COVID-19: The question of genetic diversity and therapeutic intervention approaches Genetics and Molecular Biology · 2021 · 4 citations
    3. Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation Journal of Clinical and Investigative Dermatology · 2026
    4. General Dermatology Springer eBooks · 2017
    5. Severe cutaneous adverse reactions to drugs The Lancet · 2017 · 273 citations
    6. Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty Endocrine journal · 2022
    7. Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings Scholars Journal of Medical Case Reports · 2021
    8. Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation Dermatologica Sinica · 2010 · 3 citations
    9. The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice bioRxiv (Cold Spring Harbor Laboratory) · 2020
    10. The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults Rheumatology · 2017 · 213 citations
    11. 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
    12. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    13. 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
    14. Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings International journal of contemporary pediatrics · 2020
    15. Mechanisms regulating skin immunity and inflammation Nature Reviews Immunology · 2014 · 610 citations
    16. Regulatory T Cells: the Many Faces of Foxp3 Journal of Clinical Immunology · 2019 · 125 citations
    17. Autoimmunity and autoimmune co-morbidities in psoriasis Immunology · 2018 · 49 citations
    18. Therapeutic strategies for treating hair loss Drug Discovery Today: Therapeutic Strategies · 2006 · 42 citations
    19. Aromatase deficiency in a male patient - Case report and review of the literature. Bone · 2016 · 36 citations
    20. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    21. Acne-Associated Syndromes Springer eBooks · 2019
    22. Genetic Defects of Female Sexual Differentiation Elsevier eBooks · 2016
    23. Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma British Journal of Dermatology · 2011 · 11 citations
    24. Alopecia Areata KARGER eBooks · 2008 · 24 citations
    25. Congenital atrichia and hypotrichosis World Journal of Pediatrics · 2011 · 11 citations
    26. A Cell Membrane-Level Approach to Cicatricial Alopecia Management: Is Caveolin-1 a Viable Therapeutic Target in Frontal Fibrosing Alopecia? Biomedicines · 2021 · 4 citations
    27. Immunopathogenesis of Primary Cicatricial Alopecia Research Portal (King's College London) · 2013
    28. Highlights from the 68th Annual Meeting of the Society of Investigative Dermatology Journal of Investigative Dermatology · 2007
    29. INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York) · 2018
    30. Studying the genetic predisposing factors in the pathogenesis of acne vulgaris Human Immunology · 2011 · 39 citations