uncoupling channel within the c-subunit ring of the F₁FO ATP synthase is the mitochondrial permeability transition pore von Alavian, Kambiz N, Beutner, Gisela, Lazrove, Emma, Sacchetti, Silvio, Park, Han-A, Licznerski, Pawel, Li, Hongmei, Nabili, Panah, Hockensmith, Kathryn, Graham, Morven, Porter, Jr, George A, Jonas, Elizabeth A

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Role of the Mitochondrial Permeability Transition in Bone Metabolism and Aging von Sautchuk, Rubens, Yu, Chen, McArthur, Matthew, Massie, Christine, Brookes, Paul S., Porter, George A., Awad, Hani, Eliseev, Roman A.

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PPARγ drives mitochondrial stress signaling and the loss of atrial cardiomyocytes in newborn mice exposed to hyperoxia von Cohen, E. David, Roethlin, Kyle, Yee, Min, Woeller, Collynn F., Brookes, Paul S., Porter, George A., O'Reilly, Michael A.

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Caspase-3 cleaved tau impairs mitochondrial function through the opening of the mitochondrial permeability transition pore von Pérez, María José, Ibarra-García-Padilla, Rodrigo, Tang, Maoping, Porter, George A., Johnson, Gail V.W., Quintanilla, Rodrigo A.

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Potassium conservation is impaired in mice with reduced renal expression of Kir4.1 von Malik, Sundeep, Lambert, Emily, Zhang, Junhui, Wang, Tong, Clark, Heather L, Cypress, Michael, Goldman, Bruce I, Porter, Jr, George A, Pena, Salvador, Nino, Wilson, Gray, Daniel A

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Dairy-origin Propionibacterium freudenreichii, turkey-origin Lactobacillus salivarius, and a Salmonella typhimurium vaccine elicit comparable colonization resistance on drug-resist... von Manjankattil, S., Dewi, G., Peichel, C., Creek, M., Bina, P., Lerohl, K., Deniz, K., Akhtar, L., Porter, R., Johnson, T.J., Noll, S., Kollanoor Johny, A.

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Coordinated metabolic responses to cyclophilin D deletion in the developing heart von Beutner, Gisela, Burris, Jonathan Ryan, Collins, Michael P., Kulkarni, Chaitanya A., Nadtochiy, Sergiy M., de Mesy Bentley, Karen L., Cohen, Ethan D., Brookes, Paul S., Porter, George A.

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Analyzing Supercomplexes of the Mitochondrial Electron Transport Chain with Native Electrophoresis, In-gel Assays, and Electroelution von Beutner, Gisela, Porter, Jr, George Arthur

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The complex genetics of hypoplastic left heart syndrome von Liu, Xiaoqin, Yagi, Hisato, Saeed, Shazina, Bais, Abha S, Gabriel, George C, Chen, Zhaohan, Peterson, Kevin A, Li, You, Schwartz, Molly C, Reynolds, William T, Saydmohammed, Manush, Gibbs, Brian, Wu, Yijen, Devine, William, Chatterjee, Bishwanath, Klena, Nikolai T, Kostka, Dennis, de Mesy Bentley, Karen L, Ganapathiraju, Madhavi K, Dexheimer, Phillip, Leatherbury, Linda, Khalifa, Omar, Bhagat, Anchit, Zahid, Maliha, Pu, William, Watkins, Simon, Grossfeld, Paul, Murray, Stephen A, Porter, George A, Tsang, Michael, Martin, Lisa J, Benson, D Woodrow, Aronow, Bruce J, Lo, Cecilia W

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This Article Corrects: “Identifying Patients at Greatest Risk of Mortality due to COVID-19: A New England Perspective” von Smith, Aaron, Fridling, Jeremy, Ibrahim, Danyal, Porter Jr, Paul

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Identifying Patients at Greatest Risk of Mortality due to COVID-19: A New England Perspective von Smith, Aaron A, Fridling, Jeremy, Ibrahim, Danyal, Porter, Jr, Paul S

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Neonatal hyperoxia inhibits proliferation and survival of atrial cardiomyocytes by suppressing fatty acid synthesis von Cohen, Ethan David, Yee, Min, Porter, Jr, George A, Ritzer, Erin, McDavid, Andrew N, Brookes, Paul S, Pryhuber, Gloria S, O'Reilly, Michael A

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The mitochondrial citrate carrier SLC25A1 regulates metabolic reprogramming and morphogenesis in the developing heart von Ohanele, Chiemela, Peoples, Jessica N., Karlstaedt, Anja, Geiger, Joshua T., Gayle, Ashley D., Ghazal, Nasab, Sohani, Fateemaa, Brown, Milton E., Davis, Michael E., Porter, George A., Faundez, Victor, Kwong, Jennifer Q.

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Caspases 3 and 7: Key Mediators of Mitochondrial Events of Apoptosis von Lakhani, Saquib A., Masud, Ali, Kuida, Keisuke, Porter, George A., Booth, Carmen J., Menal, Wajahat Z., Inayat, Irteza, Flavell, Richard A.

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Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study von Griffin, Emily L., Nees, Shannon N., Morton, Sarah U., Wynn, Julia, Patel, Nihir, Jobanputra, Vaidehi, Robinson, Scott, Kochav, Stephanie M., Tao, Alice, Andrews, Carli, Cross, Nancy, Geva, Judith, Lanzilotta, Kristen, Ritter, Alyssa, Taillie, Eileen, Thompson, Alexandra, Meyer, Chris, Akers, Rachel, King, Eileen C., Cnota, James F, Kim, Richard W., Porter, George A., Brueckner, Martina, Seidman, Christine E., Shen, Yufeng, Gelb, Bruce D., Goldmuntz, Elizabeth, Newburger, Jane W., Roberts, Amy E., Chung, Wendy K.

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Association of genetic and sulcal traits with executive function in congenital heart disease von Maleyeff, Lara, Newburger, Jane W., Wypij, David, Thomas, Nina H., Anagnoustou, Evdokia, Brueckner, Martina, Chung, Wendy K., Cleveland, John, Cunningham, Sean, Gelb, Bruce D., Goldmuntz, Elizabeth, Hagler, Donald J, Huang, Hao, King, Eileen, McQuillen, Patrick, Miller, Thomas A., Norris‐Brilliant, Ami, Porter, George A., Roberts, Amy E., Grant, P. Ellen, Im, Kiho, Morton, Sarah U.

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Reduction in Intracellular Calcium Levels Inhibits Myoblast Differentiation von Porter, Jr, George A, Makuck, Ryan F, Rivkees, Scott A

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Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease von Jang, Min Young, Patel, Parth N., Pereira, Alexandre C., Willcox, Jon A.L., Haghighi, Alireza, Tai, Angela C., Ito, Kaoru, Morton, Sarah U., Gorham, Joshua M., McKean, David M., DePalma, Steven R., Bernstein, Daniel, Brueckner, Martina, Chung, Wendy K., Giardini, Alessandro, Goldmuntz, Elizabeth, Kaltman, Jonathan R., Kim, Richard, Newburger, Jane W., Shen, Yufeng, Srivastava, Deepak, Tristani-Firouzi, Martin, Gelb, Bruce D., Porter, George A., Seidman, Christine E., Seidman, Jonathan G.

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Synthesis and Patterning of Gold Nanostructures on InP and GaAs via Galvanic Displacement von Hormozi Nezhad, Mohammad R., Aizawa, Masato, Porter Jr, Lon A., Ribbe, Alexander E., Buriak, Jillian M.

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A 235 Kb deletion at 17q21.33 encompassing the COL1A1, and two additional secondary copy number variants in an infant with type I osteogenesis imperfecta: A rare case report von Numbere, Numbereye, Weber, David R., Porter, George, Iqbal, Mohammed A.

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