Results 111 to 120 of about 1,103,157 (202)

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Corrigendum: Re-expression of tafazzin isoforms in TAZ-deficient C6 glioma cells restores cardiolipin composition but not proliferation rate and alterations in gene expression

open access: yesFrontiers in Genetics, 2022
Gayatri Jagirdar   +11 more
doaj   +1 more source

Tafazzin-deficient zebrafish display mitochondrial dysfunction, neutropenia, and metabolic defects without myopathy

open access: yesScientific Reports
Barth syndrome is an X-linked syndrome characterized by cardiomyopathy, skeletal myopathy, and neutropenia. This life-threatening disorder results from loss-of-function mutations in TAFAZZIN, which encodes a phospholipid-lysophospholipid transacylase ...
Usua Oyarbide   +10 more
doaj   +1 more source

Stimulating the sir2–spargel axis rescues exercise capacity and mitochondrial respiration in a Drosophila model of Barth syndrome

open access: yesDisease Models & Mechanisms, 2022
Deena Damschroder   +5 more
doaj   +1 more source

Reading: John Barth

open access: yes, 1975
In this audiovisual recording from Friday, March 21, 1975, as part of the 6th Annual UND Writers Conference: “Spirit of Place,” John Barth lectures on his aesthetics and reads a selection of his published and new fiction.
Barth, John
core   +1 more source

Mitochondrial Respiratory Chain Supercomplexes Are Destabilized in Barth Syndrome Patients

open access: yes, 2006
Mutations in the human TAZ gene are associated with Barth Syndrome, an often fatal X-linked disorder that presents with cardiomyopathy and neutropenia.
DR Thorburn (14471730)   +3 more
core  

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