Cyclophilin D, Somehow a Master Regulator of Mitochondrial Function

por Porter, George A., Beutner, Gisela
Publicado 2018

Gold salts, D-penicillamine and allopurinol

por Ueda, Shiro, Porter, George A.
Publicado 2008

Initiation of Electron Transport Chain Activity in the Embryonic Heart Coincides with the Activation of Mitochondrial Complex 1 and the Formation of Supercomplexes

por Beutner, Gisela, Eliseev, Roman A., Porter, George A.
Publicado 2014

Cyclophilin D regulates the dynamic assembly of mitochondrial ATP synthase into synthasomes

por Beutner, Gisela, Alanzalon, Ryan E., Porter, George A.
Publicado 2017

Bcl-xL in neuroprotection and plasticity

por Jonas, Elizabeth A., Porter, George A., Alavian, Kambiz N.
Publicado 2014

Extraembryonic but not embryonic SUMO-specific protease 2 is required for heart development

por Maruyama, Eri O., Lin, Heng, Chiu, Shang-Yi, Yu, H.-M. Ivy, Porter, George A., Hsu, Wei
Publicado 2016

Transcriptional regulation of cyclophilin D by BMP/Smad signaling and its role in osteogenic differentiation

por Sautchuk, Rubens, Kalicharan, Brianna H, Escalera-Rivera, Katherine, Jonason, Jennifer H, Porter, George A, Awad, Hani A, Eliseev, Roman A
Publicado 2022

Neonatal hyperoxia inhibits proliferation and survival of atrial cardiomyocytes by suppressing fatty acid synthesis

por Cohen, Ethan David, Yee, Min, Porter, George A., Ritzer, Erin, McDavid, Andrew N., Brookes, Paul S., Pryhuber, Gloria S., O’Reilly, Michael A.
Publicado 2021

A reversible mitochondrial complex I thiol switch mediates hypoxic avoidance behavior in C. elegans

por Onukwufor, John O., Farooqi, M. Arsalan, Vodičková, Anežka, Koren, Shon A., Baldzizhar, Aksana, Berry, Brandon J., Beutner, Gisela, Porter, George A., Belousov, Vsevolod, Grossfield, Alan, Wojtovich, Andrew P.
Publicado 2022

Mitochondrial Oxidative Phosphorylation defect in the Heart of Subjects with Coronary Artery Disease

por Ait-Aissa, Karima, Blaszak, Scott C., Beutner, Gisela, Tsaih, Shirng-Wern, Morgan, Garrett, Santos, Janine H., Flister, Michael J., Joyce, David L., Camara, Amadou K. S., Gutterman, David D., Donato, Anthony J., Porter, George A., Beyer, Andreas M.
Publicado 2019

The Congenital Heart Disease Genetic Network Study: Cohort description

por Hoang, Thanh T., Goldmuntz, Elizabeth, Roberts, Amy E., Chung, Wendy K., Kline, Jennie K., Deanfield, John E., Giardini, Alessandro, Aleman, Adolfo, Gelb, Bruce D., Mac Neal, Meghan, Porter, George A., Kim, Richard, Brueckner, Martina, Lifton, Richard P., Edman, Sharon, Woyciechowski, Stacy, Mitchell, Laura E., Agopian, A. J.
Publicado 2018

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

por Martin-Trujillo, Alejandro, Patel, Nihir, Richter, Felix, Jadhav, Bharati, Garg, Paras, Morton, Sarah U., McKean, David M., DePalma, Steven R., Goldmuntz, Elizabeth, Gruber, Dorota, Kim, Richard, Newburger, Jane W., Porter, George A., Giardini, Alessandro, Bernstein, Daniel, Tristani-Firouzi, Martin, Seidman, Jonathan G., Seidman, Christine E., Chung, Wendy K., Gelb, Bruce D., Sharp, Andrew J.
Publicado 2020

Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease

por Morton, Sarah U., Shimamura, Akiko, Newburger, Peter E., Opotowsky, Alexander R., Quiat, Daniel, Pereira, Alexandre C., Jin, Sheng Chih, Gurvitz, Michelle, Brueckner, Martina, Chung, Wendy K., Shen, Yufeng, Bernstein, Daniel, Gelb, Bruce D., Giardini, Alessandro, Goldmuntz, Elizabeth, Kim, Richard W., Lifton, Richard P., Porter, George A., Srivastava, Deepak, Tristani-Firouzi, Martin, Newburger, Jane W., Seidman, J. G., Seidman, Christine E.
Publicado 2020

EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

por Hsieh, Alexander, Morton, Sarah U., Willcox, Jon A. L., Gorham, Joshua M., Tai, Angela C., Qi, Hongjian, DePalma, Steven, McKean, David, Griffin, Emily, Manheimer, Kathryn B., Bernstein, Daniel, Kim, Richard W., Newburger, Jane W., Porter, George A., Srivastava, Deepak, Tristani-Firouzi, Martin, Brueckner, Martina, Lifton, Richard P., Goldmuntz, Elizabeth, Gelb, Bruce D., Chung, Wendy K., Seidman, Christine E., Seidman, J. G., Shen, Yufeng
Publicado 2020

Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency

por Ward, Tarsha, Tai, Warren, Morton, Sarah, Impens, Francis, Van Damme, Petra, Van Haver, Delphi, Timmerman, Evy, Venturini, Gabriela, Zhang, Kehan, Jang, Min Young, Willcox, Jon A.L., Haghighi, Alireza, Gelb, Bruce D., Chung, Wendy K., Goldmuntz, Elizabeth, Porter, George A., Lifton, Richard P., Brueckner, Martina, Yost, H. Joseph, Bruneau, Benoit G., Gorham, Joshua, Kim, Yuri, Pereira, Alexandre, Homsy, Jason, Benson, Craig C., DePalma, Steven R., Varland, Sylvia, Chen, Christopher S., Arnesen, Thomas, Gevaert, Kris, Seidman, Christine, Seidman, J.G.
Publicado 2021

De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease

por Boskovski, Marko T., Homsy, Jason, Nathan, Meena, Sleeper, Lynn A., Morton, Sarah, Manheimer, Kathryn B., Tai, Angela, Gorham, Joshua, Lewis, Matthew, Swartz, Michael, Alfieris, George M., Bacha, Emile A., Karimi, Mohsen, Meyer, David, Nguyen, Khanh, Bernstein, Daniel, Romano-Adesman, Angela, Porter, George A., Goldmuntz, Elizabeth, Chung, Wendy K., Srivastava, Deepak, Kaltman, Jonathan R., Tristani-Firouzi, Martin, Lifton, Richard, Roberts, Amy E., Gaynor, J. William, Gelb, Bruce D., Kim, Richard, Seidman, Jonathan G., Brueckner, Martina, Mayer, John E., Newburger, Jane W., Seidman, Christine E.
Publicado 2020

Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease

por Morton, Sarah U., Norris-Brilliant, Ami, Cunningham, Sean, King, Eileen, Goldmuntz, Elizabeth, Brueckner, Martina, Miller, Thomas A., Thomas, Nina H., Liu, Chunyan, Adams, Heather R., Bellinger, David C., Cleveland, John, Cnota, James F., Dale, Anders M., Frommelt, Michele, Gelb, Bruce D., Grant, P. Ellen, Goldberg, Caren S., Huang, Hao, Kuperman, Joshua M., Li, Jennifer S., McQuillen, Patrick S., Panigrahy, Ashok, Porter, George A., Roberts, Amy E., Russell, Mark W., Seidman, Christine E., Tivarus, Madalina E., Anagnoustou, Evdokia, Hagler, Donald J., Chung, Wendy K., Newburger, Jane W.
Publicado 2023

Genomic analyses implicate noncoding de novo variants in congenital heart disease

por Richter, Felix, Morton, Sarah U., Won Kim, Seong, Kitaygorodsky, Alexander, Wasson, Lauren K., Chen, Kathleen M., Zhou, Jian, Qi, Hongjian, Patel, Nihir, DePalma, Steven R., Parfenov, Michael, Homsy, Jason, Gorham, Joshua M., Manheimer, Kathryn B., Velinder, Matthew, Farrell, Andrew, Marth, Gabor, Schadt, Eric E., Kaltman, Jonathan R., Newburger, Jane W., Giardini, Alessandro, Goldmuntz, Elizabeth, Brueckner, Martina, Kim, Richard, Porter, George A., Bernstein, Daniel, Chung, Wendy K., Srivastava, Deepak, Tristani-Firouzi, Martin, Troyanskaya, Olga G., Dickel, Diane E., Shen, Yufeng, Seidman, Jonathan G., Seidman, Christine E., Gelb, Bruce D.
Publicado 2020

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

por Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R., Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C., Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D., Castaldi, Christopher, Tikhonoa, Irina R., Bilguvar, Kaya, Mane, Shrikant M., Sanders, Stephan J., Mital, Seema, Russell, Mark, Gaynor, William, Deanfield, John, Giardini, Alessandro, Porter, George A., Srivastava, Deepak, Lo, Cecelia W., Shen, Yufeng, Watkins, W. Scott, Yandell, Mark, Yost, H. Joseph, Tristani-Firouzi, Martin, Newburger, Jane W., Roberts, Amy E., Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R., Goldmuntz, Elizabeth, Chung, Wendy K., Seidman, Jonathan G., Gelb, Bruce D., Seidman, Christine E., Lifton, Richard P., Brueckner, Martina
Publicado 2017