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المؤلفون: Frédéric M. Vaz, Thomas Landes, Patrice X. Petit, Guillaume Vial, Pascale Bellenguer, Nellie Taleux, Christian Slomianny, Jean-Philippe Puech, Francois Gonzalvez, Ian M. Møller, Marilena D'Aurelio, Marie Boutant, Giovanni Manfredi, Aoula Moustapha, Eyal Gottlieb, Ronald J.A. Wanders, Laeticia Arnauné-Pelloquin, Riekelt H. Houtkooper
المساهمون: AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Laboratory Genetic Metabolic Diseases
المصدر: Gonzalvez, F, D'Aurelio, M, Boutant, M, Moustapha, A, Puech, J-P, Landes, T, Arnauné-Pelloquin, L, Vial, G, Taleux, N, Slomianny, C, Wanders, R J, Houtkooper, R H, Bellenguer, P, Møller, I M, Gottlieb, E, Vaz, F M, Manfredi, G & Petit, P X 2013, ' Barth syndrome : cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation ', B B A-Molecular Basis of Disease, vol. 1832, no. 8, pp. 1194-1206 . https://doi.org/10.1016/j.bbadis.2013.03.005
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1832(8), 1194-1206. Elsevierمصطلحات موضوعية: Cardiolipins, Tafazzin, Respiratory chain, Apoptosis, Citrate (si)-Synthase, Biology, Mitochondrion, Cell Line, chemistry.chemical_compound, Adenosine Triphosphate, Superoxides, medicine, Cardiolipin, Humans, Citrate synthase, Respiratory complex, Lymphocytes, Molecular Biology, Caspase 8, Cell Death, Monolysocardiolipin, Barth syndrome, medicine.disease, Mitochondria, Cell biology, Electron Transport Chain Complex Proteins, chemistry, Barth Syndrome, Mutation, Respirasome, biology.protein, Molecular Medicine, Lysophospholipids, Reactive oxygen species, Acyltransferases, Signal Transduction, Transcription Factors