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    Research 61–90 of 1000+

    1. Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways InTech eBooks · 2017 · 1 citations
    2. 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
    3. ER-located Ca2+ ATPase ACA2 regulates Ca2+ cytoplasmic pool linked to root hair growth in Arabidopsis thaliana bioRxiv (Cold Spring Harbor Laboratory) · 2026
    4. Guía de Procedimientos en Cirugía Plástica Reconstructiva Vol. 4 Juan Cuevas eBooks · 2023
    5. K <sub>ATP</sub> Channels and Cardiovascular Disease Circulation Research · 2013 · 144 citations
    6. Hair coat characteristics in Friesian heifers in the Netherlands and Kenya : experimental data and a review of literature 1978 · 12 citations
    7. Scalp Advancement and the Pretrichial Brow Lift Facial Plastic Surgery · 2018 · 10 citations
    8. Cellular therapeutics and immunotherapies in wound healing – on the pulse of time? 2024
    9. Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype Journal of Investigative Dermatology · 1999 · 62 citations
    10. A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix Human Genetics · 1997 · 100 citations
    11. Is the Loose Anagen Hair Syndrome a Keratin Disorder? Archives of Dermatology · 2002 · 84 citations
    12. A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients Journal of Investigative Dermatology · 1998 · 34 citations
    13. Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression Experimental Dermatology · 1998 · 26 citations
    14. 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
    15. Hair follicle-specific keratins and their diseases Experimental cell research · 2007 · 138 citations
    16. An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2006 · 97 citations
    17. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations
    18. Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix Journal of Investigative Dermatology · 1999 · 20 citations
    19. EBS in Children with De Novo Pathogenic Variants Disturbing Krt14 International journal of molecular sciences · 2024
    20. The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine Cosmetics · 2024
    21. Alopezien und Hypotrichosen im Kindesalter Der Hautarzt · 2014 · 5 citations
    22. Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice Journal of Investigative Dermatology · 1998 · 22 citations
    23. Transient skin stretching stimulates immune surveillance and promotes vaccine delivery via hair follicles Cell Reports · 2025
    24. The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth 2018 · 109 citations
    25. SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation Frontiers in Immunology · 2024 · 26 citations
    26. <i>ZmSPL10</i>, <i>ZmSPL14</i> and <i>ZmSPL26</i> act together to promote stigmatic papilla formation in maize through regulating auxin signaling and <i>ZmWOX3A</i> expression New Phytologist · 2024 · 1 citations
    27. Chirality Effect on Physical and Biological Properties of Peptide-Based Hydrogels Gels · 2026
    28. Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia Archives of Dermatological Research · 2024
    29. Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets Arquivos Brasileiros de Endocrinologia & Metabologia · 2008 · 24 citations
    30. Foxn1 in Skin Development, Homeostasis and Wound Healing International Journal of Molecular Sciences · 2018 · 21 citations