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    Research 91–120 of 1000+

    1. Endocrine controls of keratin expression BioEssays · 2009 · 54 citations
    2. A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13 Human Molecular Genetics · 1995 · 54 citations
    3. Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases? BioEssays · 2014 · 26 citations
    4. Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles Journal of Investigative Dermatology · 2003 · 60 citations
    5. Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin Biochemistry and Cell Biology · 1995 · 25 citations
    6. Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes Biochemical and Biophysical Research Communications · 2000 · 12 citations
    7. Biochemical examination of fetal skin biopsy specimens obtained by fetoscopy: Use of the method for analysis of keratins and filaggrin Prenatal Diagnosis · 1986 · 7 citations
    8. Keratin 71 Mutations: From Water Dogs to Woolly Hair 2012 · 11 citations
    9. Identification and characterization of genes for skin and hair disorders bonndoc (University of Bonn) · 2026
    10. A missense mutation in the type II hair keratin hHb3 is associated with monilethrix Journal of Medical Genetics · 2005 · 79 citations
    11. Mutation analysis of type II hair keratin gene in a pedigree with monilethrix Chinese Journal of Dermatology · 2010
    12. Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel Archives of Dermatological Research · 1976 · 4 citations
    13. HOW WIGS AND WOMEN’S BEAUTY SUPPLY PRODUCTS MOVE THROUGHOUT THE SUPPLY CHAIN International Supply Chain Technology Journal · 2017
    14. Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix Journal of Investigative Dermatology · 2001 · 130 citations
    15. Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture The American Journal of Human Genetics · 2010 · 97 citations
    16. Sebaceous gland diseases: clinical picture risk factors and treatment International Journal of Community Medicine and Public Health · 2023
    17. Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response Journal of Investigative Dermatology Symposium Proceedings · 2003 · 148 citations
    18. Pathogenesis of pili annulati Archives of Dermatological Research · 1988 · 36 citations
    19. Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix Experimental Dermatology · 2015 · 18 citations
    20. Alopecia totalis in an infant Cosmoderma · 2023
    21. A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1 Journal of Investigative Dermatology · 1998 · 47 citations
    22. Keratins and skin disease 2015 · 69 citations
    23. 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
    24. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    25. Establishment and characterization of a canine keratinocyte organoid culture system Veterinary Dermatology · 2018 · 34 citations
    26. Circle hairs involving the extremities in a young girl International Journal of Trichology · 2018 · 1 citations
    27. Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex International Journal of Molecular Sciences · 2021 · 40 citations
    28. A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients Journal of Investigative Dermatology · 1998 · 34 citations
    29. Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis PLoS ONE · 2014 · 21 citations
    30. KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies European journal of human genetics · 2022 · 3 citations