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• W2019978707 abstract "Lamins A and C, encoded by the LMNA gene, are nuclear proteins expressed in all post-mitotic cells. Together with B-type lamins, they form a meshwork of proteins beneath the inner nuclear membrane, the lamina, in connection with the cytoskeleton. Lamins A/C also interact with chromatin and numerous proteins, including transcription factors. Mutations in LMNA are responsible for more than ten different disorders, commonly called laminopathies. These diseases affect tissues in a specific (striated muscle, adipose tissue, peripheral nerve) or in a systemic manner (premature ageing syndromes). This wide spectrum of phenotypes is associated to a wide variety of mutations. This large clinical and genetic heterogeneity, unique to the LMNA gene, makes genotype-phenotype relations particularly difficult to establish. However, correlations have been obtained in several cases. Hence, LMNA mutations identified in premature ageing syndromes lead to the accumulation of immature proteins with a toxic effect for cells. Mutations in laminopathies of the adipose tissue mainly localize in the Ig-like domain of the proteins, potentially affecting the interaction with the SREBP-1 transcription factor. In laminopathies of the striated muscles, the mutations are spread throughout the gene. These mutations are thought to induce structural modifications of the proteins, thereby affecting their polymerization into nuclear lamina. Such defect would lead to a mechanical weakness of the nuclear lamina and of the cells, particularly in striated muscles continuously stretching. The exploration of pathophysiological mechanisms of LMNA mutations largely benefits from the numerous mouse models created, which have been widely used to analyze affected molecular pathways and to test putative therapeutic treatments." @default.
• W2019978707 created "2016-06-24" @default.
• W2019978707 creator A5009194217 @default.
• W2019978707 creator A5031640092 @default.
• W2019978707 creator A5048371134 @default.
• W2019978707 creator A5062086232 @default.
• W2019978707 date "2011-01-01" @default.
• W2019978707 modified "2023-09-23" @default.
• W2019978707 title "Laminopathies : un seul gène, de nombreuses pathologies" @default.
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• W2019978707 doi "https://doi.org/10.1051/jbio/2011017" @default.
• W2019978707 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21982404" @default.
• W2019978707 hasPublicationYear "2011" @default.
• W2019978707 type Work @default.

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