Will children reveal their secret? The coronavirus dilemma

por Porter, George James
Publicado 2020

Should lockdown be based on age rather than geography?

por Porter, George James
Publicado 2021

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

A systematic review of qualitative literature on antimicrobial stewardship in Sub-Saharan Africa

por Porter, George James, Owens, Stephen, Breckons, Matthew
Publicado 2021

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

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

por Numbere, Numbereye, Weber, David R., Porter, George, Iqbal, Mohammed A.
Publicado 2020

Reporting quality of surgical randomised controlled trials in head and neck cancer: a systematic review

por Canagarajah, Netanya Aarabi, Porter, George James, Mitra, Kurchi, Chu, Timothy Shun Man
Publicado 2021

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

Health and socioeconomic resource provision for older people in South Asian countries: Bangladesh, India, Nepal, Pakistan and Sri Lanka evidence from NEESAMA

por Matthews, Natasha Roya, Porter, George James, Varghese, Mathew, Sapkota, Nidesh, Khan, Murad Moosa, Lukose, Ammu, Paddick, Stella-Maria, Dissanayake, Malathie, Khan, Naila Zaman, Walker, Richard
Publicado 2022

Neonatal hypoxic ischemic encephalopathy increases acute kidney injury urinary biomarkers in a rat model

por Groves, Angela M., Johnston, Carl J., Beutner, Gisela G., Dahlstrom, Jane E., Koina, Mark, O'Reilly, Michael A., Porter, George, Brophy, Patrick D., Kent, Alison L.
Publicado 2022

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