Reduced protein kinase C delta in a high molecular weight complex in mitochondria and elevated creatine uptake into Barth syndrome B lymphoblasts. [PDF]
J Transl Genet GenomMejia EM +3 more
europepmc +1 more source
Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth syndrome. [PDF]
Hum Mol GenetSniezek Carney O +8 more
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What are the symptoms and concerns of young adults living with life-limiting conditions and how well are they captured by patient reported outcome measures? A mixed-methods systematic review and framework synthesis. [PDF]
Palliat MedChambers RL +4 more
europepmc +1 more source
Proteolytic regulation of mitochondrial magnesium channel by m-AAA protease and prohibitin complex. [PDF]
GeneticsJoshi A +3 more
europepmc +1 more source
Temporal Effects of Safflower Oil Diet-Based Linoleic Acid Supplementation on Barth Syndrome Cardiomyopathy. [PDF]
CirculationZhu S +10 more
europepmc +1 more source
A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice. [PDF]
Int J Mol SciSnider PL +14 more
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Tafazzin deficiency causes substantial remodeling in the lipidome of a mouse model of Barth Syndrome cardiomyopathy. [PDF]
Front Mol MedHachmann M +10 more
europepmc +1 more source
Editorial: Mitochondrial dysfunction affects mechano-energetic coupling in heart failure. [PDF]
Front Mol MedDudek J, Ritterhoff J.
europepmc +1 more source
Mitochondrial cardiolipin remodeling facilitates efficient myoblast differentiation. [PDF]
J Lipid ResOhba Y, Fujiwara CA, Arita M.
europepmc +1 more source