Pores for thought: new strategies to re-energize stressed mitochondria in acute kidney injury.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

6 citing papers in PubMed.

1. SS-31, a Mitochondria-Targeting Peptide, Ameliorates Kidney Disease.Oxidative medicine and cellular longevity · 2022
   Review
2. Dynamic multiphoton microscopy: focusing light on acute kidney injury.Physiology (Bethesda, Md.) · 2014
   Review
3. Redox-sensitive glycogen synthase kinase 3β-directed control of mitochondrial permeability transition: rheostatic regulation of acute kidney injury.Free radical biology & medicine · 2013
   Article
4. Reactive oxygen species and IRF1 stimulate IFNα production by proximal tubules during ischemic AKI.American journal of physiology. Renal physiology · 2013
   Article
5. The mitochondrial-targeted compound SS-31 re-energizes ischemic mitochondria by interacting with cardiolipin.Journal of the American Society of Nephrology : JASN · 2013
   Article
6. Endothelial pentraxin 3 contributes to murine ischemic acute kidney injury.Kidney international · 2012
   Article

Corrections and comments

• Comment on
  Mitochondria-targeted peptide accelerates ATP recovery and reduces ischemic kidney injury.2011

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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