Search
for

    Sort by

    Research 30 of 1000+

    1. The Roles of Smad2 and Smad3 in Mouse Skin Development The Knowledge Bank (The Ohio State University) · 2008
    2. Loss of ERBB2 and ERBB3 Receptors Impacts Epidermal Differentiation in Mice Journal of Investigative Dermatology · 2024
    3. Ligand-Independent Vitamin D Receptor Actions Essential for Keratinocyte Homeostasis in the Skin 2024
    4. 675 Hair loss in hephaestin knockout mice is associated with iron deficiency Journal of Investigative Dermatology · 2016
    5. KF19418, a new compound for hair growth promotion in vitro and in vivo mouse models Journal of Dermatological Science · 2001 · 15 citations
    6. Cutaneous transcriptome analysis in NIH hairless mice PloS one · 2017 · 7 citations
    7. The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling ˜The œAmerican journal of pathology · 2002 · 146 citations
    8. Making the head: Caspases in life and death Frontiers in Cell and Developmental Biology · 2023 · 7 citations
    9. The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin PLoS ONE · 2025
    10. Dysregulation of Grainyhead-like 3 expression causes widespread developmental defects Research Square (Research Square) · 2021
    11. Continuous MEK inhibition by AZD6244 (ARRY-142886) results in exhaustion of the cutaneous keratinocytic stem cell pool and resembles senescence driven skin aging Journal of Clinical Oncology · 2008 · 2 citations
    12. Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development Developmental Dynamics · 2006 · 178 citations
    13. The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation American Journal Of Pathology · 1999 · 166 citations
    14. Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions Journal of Investigative Dermatology · 2015 · 56 citations
    15. Applications of Plasma-Activated Liquid in the Medical Field Biomedicines · 2021 · 13 citations
    16. Wwox Deficiency Causes Downregulation of Prosurvival ERK Signaling and Abnormal Homeostatic Responses in Mouse Skin Frontiers in cell and developmental biology · 2020 · 6 citations
    17. PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i> 2023
    18. Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice Annals of the New York Academy of Sciences · 2023 · 3 citations
    19. LB1011 Oncogenic ras mutation induces spatiotemporally specific tissue deformation through converting fluctuated into sustained ERK activation Journal of Investigative Dermatology · 2022
    20. Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer Cells · 2020 · 22 citations
    21. Mouse models with a disrupted PTHrP gene or a disrupted PTH gene (PTH−/− mice) Bone · 2010
    22. Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese 2022
    23. Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis PloS one · 2011 · 61 citations
    24. Mutant Cx43 in Skin Differentiation and Disease 2011
    25. An inductive signalling network regulates mammalian tooth morphogenesis with implications for tooth regeneration Cell Proliferation · 2013 · 27 citations
    26. The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling Development · 2011 · 134 citations
    27. The Role of Pannexin 3 in Bone Biology Journal of Dental Research · 2016 · 32 citations
    28. Exogenous IGF-1 promotes hair growth by stimulating cell proliferation and down regulating TGF-β1 in C57BL/6 mice in vivo Growth Hormone & IGF Research · 2014 · 53 citations
    29. Epidemiological Assessment of Testosterone Levels in Women Population: A Factorial Analysis of Cell Proliferation Biology and medicine · 2018 · 2 citations
    30. WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation Nature Communications · 2017 · 96 citations