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These results suggest an interplay between mitochondrial dysfunction and epigenetic alterations, which may be a primary determinant of DOX-induced cardiotoxicity.
However, the molecular mechanisms underlying the cross-talk between mitochondrial dysfunction and autophagy remain to be further elucidated.
A close association between mitochondrial dysfunction and insulin resistance is well established [1] [3].
This implies that there is a synergistic interplay between mitochondrial dysfunction and amyloid burden that leads to hyperphosphorylation of tau.
A number of prior studies have found associations between mitochondrial dysfunction and AD, and animal models of AD [26], [44] [46].
Since several decades it has been shown that solid tumor cells are characterized by intense anaerobic glycolysis [32], strongly suggestive of an association between mitochondrial dysfunction and cancer.
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Determining the nature of the connections between mitochondrial dysfunction, ROS and pathogenic mechanisms is a burgeoning area of great importance.
Here, we investigated cause-and-effect relationships between mitochondrial dysfunction, microtubule network disruption and accumulation of autophagosomes and autophagy substrates.
We thus propose that HCCS plays a key role in central nervous system (CNS) development by modulating a novel non-canonical start-up of cell death and provide the first experimental evidence for a mechanistic link between mitochondrial dysfunction, intrinsic apoptosis and developmental disorders.
However, the link between mitochondrial dysfunction, intrinsic apoptosis and developmental anomalies has not been demonstrated to date.
IMPACT: Our results provide the first experimental evidence for a mechanistic link between mitochondrial dysfunction, intrinsic apoptosis, and developmental disorders.
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between thyroid dysfunction and
between sympathetic dysfunction and
between mitochondrial damage and
between metabolic dysfunction and
between mitochondrial fusion and
between endothelial dysfunction and
between mitochondrial mutation and
between mitochondrial activity and
between olfactory dysfunction and
between salivary dysfunction and
between mitochondrial variation and
between erectile dysfunction and
between transcriptional dysfunction and
between mitochondrial length and
between diaphragmatic dysfunction and
between neurocognitive dysfunction and
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