Assessment of mitochondrial membrane potential using an on-chip microelectrode in a microfluidic device

par Lim, Tae-Sun, Dávila, Antonio, Wallace, Douglas C., Burke, Peter
Publié 2010

D-Dimer and Fibrin Degradation Products Impair Platelet Signaling: Plasma D-Dimer Is a Predictor and Mediator of Platelet Dysfunction During Trauma

par Verni, Christopher C, Davila, Antonio, Sims, Carrie A, Diamond, Scott L
Publié dans J Appl Lab Med (2020)

Nanofluidic Platform for Single Mitochondria Analysis Using Fluorescence Microscopy

par Zand, Katayoun, Pham, Ted, Davila, Antonio, Wallace, Douglas C., Burke, Peter J.
Publié 2013

Role of SUV3 Helicase in Maintaining Mitochondrial Homeostasis in Human Cells

par Khidr, Lily, Wu, Guikai, Davila, Antonio, Procaccio, Vincent, Wallace, Douglas, Lee, Wen-Hwa
Publié 2008

Wafer-scale Mitochondrial Membrane Potential Assays

par Lim, Tae-Sun, Davila, Antonio, Zand, Katayoun, Douglas, Wallace C., Burke, Peter J.
Publié 2012

Platelet dysfunction during trauma involves diverse signaling pathways and an inhibitory activity in patient-derived plasma

par Verni, Christopher C., Davila, Antonio, Balian, Steve, Sims, Carrie A., Diamond, Scott L.
Publié dans J Trauma Acute Care Surg (2019)

Nicotinamide mononucleotide preserves mitochondrial function and increases survival in hemorrhagic shock

par Sims, Carrie A., Guan, Yuxia, Mukherjee, Sarmistha, Singh, Khushboo, Botolin, Paul, Davila, Antonio, Baur, Joseph A.
Publié dans JCI Insight (2018)

Increasing NAD Synthesis in Muscle via Nicotinamide Phosphoribosyltransferase Is Not Sufficient to Promote Oxidative Metabolism

par Frederick, David W., Davis, James G., Dávila, Antonio, Agarwal, Beamon, Michan, Shaday, Puchowicz, Michelle A., Nakamaru-Ogiso, Eiko, Baur, Joseph A.
Publié dans J Biol Chem (2015)

A novel NDUFA1 mutation leads to a progressive mitochondrial complex I- specific neurodegenerative disease

par Potluri, Prasanth, Davila, Antonio, Ruiz-Pesini, Eduardo, Mishmar, Dan, O'Hearn, Sean, Hancock, Saege, Simon, Mariella, Scheffler, Immo, Wallace, Douglas C., Procaccio, Vincent
Publié 2009

Nicotinamide adenine dinucleotide is transported into mammalian mitochondria

par Davila, Antonio, Liu, Ling, Chellappa, Karthikeyani, Redpath, Philip, Nakamaru-Ogiso, Eiko, Paolella, Lauren M, Zhang, Zhigang, Migaud, Marie E, Rabinowitz, Joshua D, Baur, Joseph A
Publié dans eLife (2018)

Purinergic glio-endothelial coupling during neuronal activity: role of P2Y(1) receptors and eNOS in functional hyperemia in the mouse somatosensory cortex

par Toth, Peter, Tarantini, Stefano, Davila, Antonio, Valcarcel-Ares, M. Noa, Tucsek, Zsuzsanna, Varamini, Behzad, Ballabh, Praveen, Sonntag, William E., Baur, Joseph A., Csiszar, Anna, Ungvari, Zoltan
Publié dans Am J Physiol Heart Circ Physiol (2015)

Testing the Oxidative Stress Hypothesis of Aging in Primate Fibroblasts: Is There a Correlation Between Species Longevity and Cellular ROS Production?

par Csiszar, Anna, Podlutsky, Andrej, Podlutskaya, Natalia, Sonntag, William E., Merlin, Steven Z., Philipp, Eva E. R., Doyle, Kristian, Davila, Antonio, Recchia, Fabio A., Ballabh, Praveen, Pinto, John T., Ungvari, Zoltan
Publié 2012

A Mutation of β-Actin That Alters Depolymerization Dynamics Is Associated with Autosomal Dominant Developmental Malformations, Deafness, and Dystonia

par Procaccio, Vincent, Salazar, Gloria, Ono, Shoichiro, Styers, Melanie L., Gearing, Marla, Davila, Antonio, Jimenez, Richard, Juncos, Jorge, Gutekunst, Claire-Anne, Meroni, Germana, Fontanella, Bianca, Sontag, Estelle, Sontag, Jean Marie, Faundez, Victor, Wainer, Bruce H.
Publié 2006

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming

par Picard, Martin, Zhang, Jiangwen, Hancock, Saege, Derbeneva, Olga, Golhar, Ryan, Golik, Pawel, O’Hearn, Sean, Levy, Shawn, Potluri, Prasanth, Lvova, Maria, Davila, Antonio, Lin, Chun Shi, Perin, Juan Carlos, Rappaport, Eric F., Hakonarson, Hakon, Trounce, Ian A., Procaccio, Vincent, Wallace, Douglas C.
Publié 2014

Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans

par Ji, Fuyun, Sharpley, Mark S., Derbeneva, Olga, Alves, Leonardo Scherer, Qian, Pin, Wang, Yaoli, Chalkia, Dimitra, Lvova, Maria, Xu, Jiancheng, Yao, Wei, Simon, Mariella, Platt, Julia, Xu, Shiqin, Angelin, Alessia, Davila, Antonio, Huang, Taosheng, Wang, Ping H., Chuang, Lee-Ming, Moore, Lorna G., Qian, Guisheng, Wallace, Douglas C.
Publié 2012

Loss of NAD homeostasis leads to progressive and reversible degeneration of skeletal muscle

par Frederick, David W., Loro, Emanuele, Liu, Ling, Davila, Antonio, Chellappa, Karthikeyani, Silverman, Ian M., Quinn, William J., Gosai, Sager J., Tichy, Elisia D., Davis, James G., Mourkioti, Foteini, Gregory, Brian D., Dellinger, Ryan W., Redpath, Philip, Migaud, Marie E., Nakamaru-Ogiso, Eiko, Rabinowitz, Joshua D., Khurana, Tejvir S., Baur, Joseph A.
Publié dans Cell Metab (2016)

Multimodality assessment of heart failure with preserved ejection fraction skeletal muscle reveals differences in the machinery of energy fuel metabolism

par Zamani, Payman, Proto, Elizabeth A., Wilson, Neil, Fazelinia, Hossein, Ding, Hua, Spruce, Lynn A., Davila, Antonio, Hanff, Thomas C., Mazurek, Jeremy A., Prenner, Stuart B., Desjardins, Benoit, Margulies, Kenneth B., Kelly, Daniel P., Arany, Zoltan, Doulias, Paschalis‐Thomas, Elrod, John W., Allen, Mitchell E., McCormack, Shana E., Schur, Gayatri Maria, D'Aquilla, Kevin, Kumar, Dushyant, Thakuri, Deepa, Prabhakaran, Karthik, Langham, Michael C., Poole, David C., Seeholzer, Steven H., Reddy, Ravinder, Ischiropoulos, Harry, Chirinos, Julio A.
Publié dans ESC Heart Fail (2021)

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

par Simon, Mariella, Richard, Elodie M., Wang, Xinjian, Shahzad, Mohsin, Huang, Vincent H., Qaiser, Tanveer A., Potluri, Prasanth, Mahl, Sarah E., Davila, Antonio, Nazli, Sabiha, Hancock, Saege, Yu, Margret, Gargus, Jay, Chang, Richard, Al-sheqaih, Nada, Newman, William G., Abdenur, Jose, Starr, Arnold, Hegde, Rashmi, Dorn, Thomas, Busch, Anke, Park, Eddie, Wu, Jie, Schwenzer, Hagen, Flierl, Adrian, Florentz, Catherine, Sissler, Marie, Khan, Shaheen N., Li, Ronghua, Guan, Min-Xin, Friedman, Thomas B., Wu, Doris K., Procaccio, Vincent, Riazuddin, Sheikh, Wallace, Douglas C., Ahmed, Zubair M., Huang, Taosheng, Riazuddin, Saima
Publié dans PLoS Genet (2015)