Publications
Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathy
Kwong JQ, Davis J, Baines CP, Sargent MA, Karch J, Wang X, Huang T, Molkentin JD (2014) Cell Death & Differentiation
Apoptosis repressor with a CARD domain (ARC) restrains Bax-mediated pathogenesis in dystrophic skeletal muscle
Davis J, Kwong JQ, Kitsis RN, Molkentin JD (2013) PLoS One
Bax and Bak function as the outer membrane component of the mitochondrial permeability pore in regulating necrotic cell death in mice
Karch J, Kwong JQ, Burr AR, Sargent MA, Elrod JW, Peixoto PM, Martinez-Caballero S, Osinska H, Cheng EH, Robbins J, Kinnally KW, Molkentin JD (2013) Elife
The mitochondrial respiratory chain is a modulator of apoptosis
Kwong JQ, Henning MS, Starkov AA, Manfredi G (2007) Journal of Cell Biology
The role of mitochondria in inherited neurodegenerative diseases
Kwong JQ, Beal MF, Manfredi G (2006) Journal of Neurochemistry
Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis
Shidara Y, Yamagata K, Kanamori T, Nakano K, Kwong JQ, Manfredi G, Oda H, Ohta S (2005) Cancer Research
BCL-2 improves oxidative phosphorylation and modulates adenine nucleotide translocation in mitochondria of cells harboring mutant mtDNA
Manfredi G, Kwong JQ, Oca-Cossio JA, Woischnik M, Gajewski CD, Martushova K, D'Aurelio M, Friedlich AL, Moraes CT (2003) Journal of Bioogical Chemistry
Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus
Manfredi G, Fu J, Ojaimi J, Sadlock JE, Kwong JQ, Guy J, Schon EA (2002) Nature Genetics
In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I
D'Aurelio M, Pallotti F, Barrientos A, Gajewski CD, Kwong JQ, Bruno C, Beal MF, Manfredi G (2001) Journal of Biological Chemistry
Bcl-2 suppresses oxidative phosphorylation defects caused by mitochondrial DNA mutations
Manfredi G, Kwong JQ, Oca-Cossio JA, Aurelio MD, Gajewsky CD, Beal FM, Moraes CT (2001) ScientificWorldJournal