Results 71 to 80 of about 2,246 (103)

Unrestrained fatty acid oxidation triggers heart failure in mice via cardiolipin loss and mitochondrial dysfunction. [PDF]

J Clin Invest
Kim CW, Vale G, Fu X, McDonald JG, Dai C, Li C, Wang ZV, Sharma G, Khemtong C, Malloy CR, Deja S, Burgess SC, Mitsche MA, Horton JD.   +13 more
europepmc   +1 more source

Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene. [PDF]

Prenat Diagn
Muir CR, Gilmore KL, Singh S, Vora NL.
europepmc   +1 more source

What can ATP content tell us about Barth syndrome muscle phenotypes? [PDF]

J Transl Genet Genom
Brault JJ, Conway SJ.
europepmc   +1 more source

ABHD18 degrades cardiolipin by stepwise hydrolysis of fatty acids. [PDF]

J Biol Chem
Ren M, Chen S, Greenberg ML, Schlame M.
europepmc   +1 more source

[Corrigendum] 17‑AAG synergizes with Belinostat to exhibit a negative effect on the proliferation and invasion of MDA‑MB‑231 breast cancer cells. [PDF]

Oncol Rep
Zuo Y, Xu H, Chen Z, Xiong F, Zhang B, Chen K, Jiang H, Luo C, Zhang H.   +8 more
europepmc   +1 more source

Expanding the phenotypic and genetic landscape of congenital neutropenia through whole-exome and genome sequencing. [PDF]

Hemasphere
Marti S, Pellet P, Beaupain B, Durix L, Buratti J, Réguerre Y, Aladjidi N, Azarnoush S, Clauin S, Chahla WA, Blaison G, Bertand J, Bodet D, Brethon B, Chane-Teng J, Delafoy M, Dupraz C, Gandemer V, Denizeau P, Goldenberg A, Hirsch P, l'Haridon A, Marie-Cardine A, Vera G, Nelken B, Nizery L, Nolla M, Pasquet M, Rosain J, Terriou L, Plo I, Donadieu J, Bellanné-Chantelot C.   +32 more
europepmc   +1 more source

Cardiolipin and mitochondrial membrane integrity in neurodegeneration: insights from α-synuclein-driven Parkinson's disease. [PDF]

Acta Neuropathol Commun
Ruiz-Ortega ED, Wilkaniec A, Juárez J, Adamczyk A.   +3 more
europepmc   +1 more source

Analysis of neuronal cardiolipin and monolysocardiolipin from biological samples with cyclic ion mobility mass spectrometry. [PDF]

Front Physiol
Emaus KJ, Dunbar CA, Caruso J, Ruotolo BT, Wider JM, Sanderson TH.   +5 more
europepmc   +1 more source

3D bioprinted myocardium patches for rare Barth syndrome: TAZ mutation correction in cardioblasts. [PDF]

Ann Med Surg (Lond)
Tahir A, Imtiaz E, Mahato RK.
europepmc   +1 more source