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François Taddei

Researcher at Paris Descartes University

Publications -  96
Citations -  10684

François Taddei is an academic researcher from Paris Descartes University. The author has contributed to research in topics: Population & Gene. The author has an hindex of 46, co-authored 95 publications receiving 9916 citations. Previous affiliations of François Taddei include French Institute of Health and Medical Research & École Normale Supérieure.

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Robust growth of Escherichia coli.

TL;DR: The long-term growth and division patterns of Escherichia coli cells are studied by employing a microfluidic device designed to follow steady-state growth anddivision of a large number of cells at a defined reproductive age to conclude that E. coli has a robust mechanism of growth that is decoupled from cell death.
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Stress-Induced Mutagenesis in Bacteria

TL;DR: It is suggested that irrespective of the causes of their emergence, stress-induced mutations participate in adaptive evolution and could be a by-product of genetic strategies for improving survival under stress.
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Role of mutator alleles in adaptive evolution

TL;DR: Whether high mutation rates might play an important role in adaptive evolution is considered, as models of large, asexual, clonal populations adapting to a new environment show that strong mutator genes can accelerate adaptation, even if the mutator gene remains at a very low frequency.
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Aging and Death in an Organism That Reproduces by Morphologically Symmetric Division

TL;DR: It is concluded that the two supposedly identical cells produced during cell division are functionally asymmetric; the old pole cell should be considered an aging parent repeatedly producing rejuvenated offspring and therefore immortality may be either too costly or mechanistically impossible in natural organisms.
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Asymmetric segregation of protein aggregates is associated with cellular aging and rejuvenation

TL;DR: This work followed the appearance and inheritance of spontaneous protein aggregation within lineages of Escherichia coli grown under nonstressed conditions using time-lapse microscopy and a fluorescently tagged chaperone involved in aggregate processing to faithfully identify in vivo the localization of aggregated proteins.