Sentence examples for be specific for mitochondrial from inspiring English sources

Taken together, the effect of mitochondrial uncoupling seems to be specific for mitochondrial p53 accumulation and non-transcriptional p53 activities.

We capitalized on the specificity of RhodZin-3 and FluoZin-3, Zn-specific fluorophores which are specific for mitochondrial and "labile" Zn pools in vesicles to explore this hypothesis.

In accordance with evidence shown (Fig. 5D) for specific p53 deacetylation, we tested whether the SirT3 lysine deacetylase activity from human embryonic lung fibroblasts IMR-90 transduced with the MSCV-SirT3 retrovirus is specific for mitochondrial p53.

This emphasizes the necessity for developing more bioinformatics tools that are specific for mitochondrial genome analysis.

The low-speed pellet (Pm/N) was positive for both plasma membrane (Na K ATPase) and nuclear (PCNA) markers, but negative for cytosolic (GAPDH) and mitochondrial (F1 ATP synthase β subunit); the high-speed pellet (M) was specific for mitochondrial proteins, while the high speed supernatant (C) was positive only for cytosolic markers.

To determine whether autophagy was specific for mitochondria, we first examined mitochondrial mass in BMCs derived from FM patients.

The effect was specific for OPA1 since degradation of other mitochondrial protein, including Hsp60, ATP synthase and Tims and Toms was not observed (data not shown).

Thus, although both Ames and WT mice experience these age-associated down regulations of CI and CIV activities, we propose that these mitochondrial changes are specific for WT (ROS) and dwarf (decreased levels of oxidative stress).

Electron microscopy (EM) may also be performed on muscle specimens and demonstrate a variety of abnormalities associated with MM, although these are rarely specific for mitochondrial diseases.

And so while there is some thought that CVS is genetically distinct based on onset of disease, the association with migraine, high KSP scores in adult-onset CVS which are specific and sensitive for mitochondrial dysfunction and similar response to treatment suggests otherwise and underscores the need for further analysis [ 9, 10].

For example, there are specific regions of the mitochondrial genome that have corresponding nuclear mitochondrial pseudogenes (numts) distributed across multiple chromosomes.