Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases

by Wallace, Douglas C.
Published 2013

Microchambers with Solid-State Phosphorescent Sensor for Measuring Single Mitochondrial Respiration

by Pham, Ted D., Wallace, Douglas C., Burke, Peter J.
Published 2016

Genetic analysis of dTSPO, an outer mitochondrial membrane protein, reveals its functions in apoptosis, longevity, and Aβ42-induced neurodegeneration

by Lin, Ran, Angelin, Alessia, Da Settimo, Federico, Martini, Claudia, Taliani, Sabrina, Zhu, Shigong, Wallace, Douglas C
Published 2014

TSPO, a Mitochondrial Outer Membrane Protein, Controls Ethanol-Related Behaviors in Drosophila

by Lin, Ran, Rittenhouse, Danielle, Sweeney, Katelyn, Potluri, Prasanth, Wallace, Douglas C.
Published 2015

Peripheral Blood Mitochondrial DNA as a Biomarker of Cerebral Mitochondrial Dysfunction following Traumatic Brain Injury in a Porcine Model

by Kilbaugh, Todd J., Lvova, Maria, Karlsson, Michael, Zhang, Zhe, Leipzig, Jeremy, Wallace, Douglas C., Margulies, Susan S.
Published 2015

Succinate Dehydrogenase Is a Direct Target of Sirtuin 3 Deacetylase Activity

by Finley, Lydia W. S., Haas, Wilhelm, Desquiret-Dumas, Valérie, Wallace, Douglas C., Procaccio, Vincent, Gygi, Steven P., Haigis, Marcia C.
Published 2011

TGF-β1 induction of the adenine nucleotide translocator 1 in astrocytes occurs through Smads and Sp1 transcription factors

by Law, Alick KT, Gupta, Deepak, Levy, Shawn, Wallace, Douglas C, McKeon, Robert J, Buck, Charles R
Published 2004

MITOMAP: a human mitochondrial genome database—2004 update

by Brandon, Marty C., Lott, Marie T., Nguyen, Kevin Cuong, Spolim, Syawal, Navathe, Shamkant B., Baldi, Pierre, Wallace, Douglas C.
Published 2005

Cristae remodeling causes acidification detected by integrated graphene sensor during mitochondrial outer membrane permeabilization

by Pham, Ted D., Pham, Phi Q., Li, Jinfeng, Letai, Anthony G., Wallace, Douglas C., Burke, Peter J.
Published 2016

Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages

by Schurr, Theodore G., Ballinger, Scott W., Gan, Yik Yuen, Hodge, Judith A., Merriwether, David Andrew, Lawrence, Dale N., Knowler, William C., Weiss, Kenneth M., Wallace, Douglas C.
Published 1990

An enhanced MITOMAP with a global mtDNA mutational phylogeny

by Ruiz-Pesini, Eduardo, Lott, Marie T., Procaccio, Vincent, Poole, Jason C., Brandon, Marty C., Mishmar, Dan, Yi, Christina, Kreuziger, James, Baldi, Pierre, Wallace, Douglas C.
Published 2007

The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment

by Yarosh, Will, Monserrate, Jessica, Tong, James Jiayuan, Tse, Stephanie, Le, Phung Khanh, Nguyen, Kimberly, Brachmann, Carrie B, Wallace, Douglas C, Huang, Taosheng
Published 2008

Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespan

by Chen, Phang-Lang, Chen, Chi-Fen, Chen, Yumay, Guo, Xuning Emily, Huang, Chun-Kai, Shew, Jin-Yuh, Reddick, Robert L., Wallace, Douglas C., Lee, Wen-Hwa
Published 2012

An Inherited Heteroplasmic Mutation in Mitochondrial Gene COI in a Patient with Prostate Cancer Alters Reactive Oxygen, Reactive Nitrogen and Proliferation

by Arnold, Rebecca S., Sun, Qian, Sun, Carrie Q., Richards, Jendai C., O'Hearn, Sean, Osunkoya, Adeboye O., Wallace, Douglas C., Petros, John A.
Published 2013

Acute exercise remodels mitochondrial membrane interactions in mouse skeletal muscle

by Picard, Martin, Gentil, Benoit J., McManus, Meagan J., White, Kathryn, St. Louis, Kyle, Gartside, Sarah E., Wallace, Douglas C., Turnbull, Douglass M.
Published 2013

Trans-mitochondrial coordination of cristae at regulated membrane junctions

by Picard, Martin, McManus, Meagan J., Csordás, György, Várnai, Péter, Dorn II, Gerald W., Williams, Dewight, Hajnóczky, György, Wallace, Douglas C.
Published 2015

Mitochondrial Mutations and Polymorphisms in Psychiatric Disorders

by Sequeira, Adolfo, Martin, Maureen V., Rollins, Brandi, Moon, Emily A., Bunney, William E., Macciardi, Fabio, Lupoli, Sara, Smith, Erin N., Kelsoe, John, Magnan, Christophe N., van Oven, Mannis, Baldi, Pierre, Wallace, Douglas C., Vawter, Marquis P.
Published 2012

Human Retinal Transmitochondrial Cybrids with J or H mtDNA Haplogroups Respond Differently to Ultraviolet Radiation: Implications for Retinal Diseases

by Malik, Deepika, Hsu, Tiffany, Falatoonzadeh, Payam, Cáceres-del-Carpio, Javier, Tarek, Mohamed, Chwa, Marilyn, Atilano, Shari R., Ramirez, Claudio, Nesburn, Anthony B., Boyer, David S., Kuppermann, Baruch D., Jazwinski, S. Michal, Miceli, Michael V., Wallace, Douglas C., Udar, Nitin, Kenney, M. Cristina
Published 2014

Targeting ACLY sensitizes castration-resistant prostate cancer cells to AR antagonism by impinging on an ACLY-AMPK-AR feedback mechanism

by Shah, Supriya, Carriveau, Whitney J., Li, Jinyang, Campbell, Sydney L., Kopinski, Piotr K., Lim, Hee-Woong, Daurio, Natalie, Trefely, Sophie, Won, Kyoung-Jae, Wallace, Douglas C., Koumenis, Constantinos, Mancuso, Anthony, Wellen, Kathryn E.
Published 2016

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

by Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I., Dyck, Peter J.
Published 2011