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Olga Goldberger

Howard Hughes Medical Institute · US
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Area of research
Molecular Biology · Clinical Biochemistry
Research interest
Research interests include Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Proteoglycans and glycosaminoglycans research, and ATP Synthase and ATPases Research.
h-index
25
citations
6,713
works
37
NIH funding
primary concept
email

Recent publications

ChREBP is activated by reductive stress and mediates GCKR-associated metabolic traits
Cell Metabolism 2023cited by 40position: middledoi
Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOS
Nature Communications 2022cited by 98position: middledoi
Hypoxia ameliorates brain hyperoxia and NAD+ deficiency in a murine model of Leigh syndrome
Molecular Genetics and Metabolism 2021cited by 31position: middledoi
Hepatic NADH reductive stress underlies common variation in metabolic traits
Nature 2020cited by 202position: middledoi
Evolutionary divergence reveals the molecular basis of EMRE dependence of the human MCU
Life Science Alliance 2020cited by 15position: middledoi
Leigh Syndrome Mouse Model Can Be Rescued by Interventions that Normalize Brain Hyperoxia, but Not HIF Activation
Cell Metabolism 2019cited by 125position: middledoi
Exploring the In Vivo Role of the Mitochondrial Calcium Uniporter in Brown Fat Bioenergetics
Cell Reports 2019cited by 43position: middledoi
Impaired hypoxic pulmonary vasoconstriction in a mouse model of Leigh syndrome
American Journal of Physiology-Lung Cellular and Molecular Physiology 2018cited by 6position: middledoi
Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome
Proceedings of the National Academy of Sciences 2017cited by 165position: middledoi
Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter
Proceedings of the National Academy of Sciences 2017cited by 69position: middledoi
Mitochondrial dysfunction remodels one-carbon metabolism in human cells
eLife 2016cited by 452position: middledoi
Hypoxia as a therapy for mitochondrial disease
Science 2016cited by 446position: middledoi
Hypoxia as a therapy for mitochondrial disease
DSpace@MIT (Massachusetts Institute of Technology) 2016cited by 3position: middle
EMRE Is an Essential Component of the Mitochondrial Calcium Uniporter Complex
Science 2013cited by 660position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Vamsi K. Mootha · Harvard University14 papers (2013–2023) · 6 papers (2016–2021)Hardik Shah · Sylvester Comprehensive Cancer Center4 papers (2020–2023)Isha H. Jain · Gladstone Institutes4 papers (2016–2019)Andrew L. Markhard · Stanford University4 papers (2013–2023)Fumito Ichinose · Harvard University4 papers (2016–2021) · 4 papers (2016–2021)Yasemin Sancak · University of Washington4 papers (2013–2020)Rohit Sharma · Vivekananda Global University4 papers (2016–2021) · 3 papers (2018–2021)Clary B. Clish · Broad Institute3 papers (2016–2023)Jun Peng · Fudan University3 papers (2016–2016)Sarah E. Calvo · Massachusetts Institute of Technology3 papers (2013–2023)Wolfram Goessling · Harvard University3 papers (2016–2016)L. Zazzeron · Harvard University3 papers (2016–2019)Gregory R. Wojtkiewicz · Harvard University2 papers (2019–2021)Steven A. Carr · Broad Institute2 papers (2013–2016)Donald B. Bloch · Case Western Reserve University2 papers (2018–2021) · 2 papers (2017–2018)Amy Deik · Broad Institute2 papers (2020–2023)
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