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    Research 361–390 of 1000+

    1. Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs Frontiers in Genetics · 2023
    2. Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations 2009 · 115 citations
    3. New-Generation Therapies for the Treatment of Hair Loss in Men Dermatologic Clinics · 2017 · 15 citations
    4. Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments BMC genomics · 2014 · 65 citations
    5. Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families The Journal of Dermatology · 2011 · 11 citations
    6. Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene Genetic testing and molecular biomarkers · 2017 · 7 citations
    7. Hair follicle transcriptome profiles during the transition from anagen to catagen in Cashmere goat (Capra hircus) Genetics and molecular research · 2015 · 14 citations
    8. Selection signatures for fiber production in commercial species: A review Animal Genetics · 2022 · 5 citations
    9. Transcriptomic analyses of regenerating adult feathers in chicken BMC Genomics · 2015 · 45 citations
    10. A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair Journal of Medical Genetics · 2015 · 29 citations
    11. Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India Journal of Natural Fibers · 2018 · 9 citations
    12. Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness Animals · 2023
    13. Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report Frontiers in genetics · 2022
    14. Disorders of Keratinization American journal of clinical dermatology · 2004 · 44 citations
    15. A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response American Journal of Medical Genetics Part A · 2021 · 5 citations
    16. Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review Egyptian Journal of Medical Human Genetics · 2019 · 49 citations
    17. Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2012
    18. Androgens and hair loss Current Opinion in Endocrinology, Diabetes and Obesity · 2009 · 52 citations
    19. Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy Experimental Dermatology · 2019 · 20 citations
    20. Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation Veterinary sciences · 2023 · 3 citations
    21. Pharmacological therapeutics in androgenetic alopecia Journal of The Korean Medical Association · 2020 · 3 citations
    22. Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens) Communications Biology · 2026
    23. Системная терапия больных андрогенетической алопецией Вестник дерматологии и венерологии · 2015
    24. Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2010
    25. Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · 2010
    26. Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair Proceedings of the National Academy of Sciences · 2008 · 115 citations
    27. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family British Journal of Dermatology · 2000 · 36 citations
    28. Current understanding of androgenetic alopecia. Part I: etiopathogenesis. PubMed · 2000 · 28 citations
    29. Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands Acta dermato-venereologica · 2017 · 4 citations
    30. Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation Cureus · 2026