Results 141 to 150 of about 3,734 (156)
Mechanostimulation-Induced Cell Adhesion and Interaction with the Extracellular Matrix. [PDF]
BiomoleculesKatoh K.
europepmc +1 more source
Co-morbid monogenic disorders at chromosome region 1q2: LMNA- and FLG-related disorders in a patient referred for assessment of joint hypermobility. [PDF]
Chromosome ResOsundiji MA, Bello AO, Hand JL.
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Laminopathies and lamin-associated signaling pathways
Journal of Cellular Biochemistry, 2011 Laminopathies are genetic diseases due to mutations or altered post-translational processing of nuclear envelope/lamina proteins. The majority of laminopathies are caused by mutations in the LMNA gene, encoding lamin A/C, but manifest as diverse ...
Cristina Capanni +2 more
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Lipodystrophic laminopathies: Diagnostic clues [PDF]
Nucleus, 2018 The nuclear lamina is a complex reticular structure that covers the inner face of the nucleus membrane in metazoan cells. It is mainly formed by intermediate filaments called lamins, and exerts essential functions to maintain the cellular viability ...
Antía Fernández-Pombo +2 more
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MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies
Aging Cell, 2018 International audienceHereditary and sporadic laminopathies are caused by mutations in genes encoding lamins, their partners, or the metalloprotease ZMPSTE24/FACE1.
Nicolas Levy, Patrice Roll
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Cardiovascular complications of lipodystrophic syndromes – focus on laminopathies
Annales D'Endocrinologie, 2021Isabelle Jéru +2 more
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Laminopathies: The molecular background of the disease and the prospects for its treatment
Cellular and Molecular Biology Letters, 2011Ryszard Rzepecki +2 more
exaly