Author details

Full Name

Olga Goldberger

Affiliation

ORCID

Career Start Year

1993

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35513392	Combinatorial GxGxE CRISPR screen identifies SLC25A39 in mitochondrial glutathione transport linking iron homeostasis to OXPHOS.	Nat Commun	2022
33752971	Hypoxia ameliorates brain hyperoxia and NAD<sup>+</sup> deficiency in a murine model of Leigh syndrome.	Mol Genet Metab	2021
32769116	Evolutionary divergence reveals the molecular basis of EMRE dependence of the human MCU.	Life Sci Alliance	2020
32461692	Hepatic NADH reductive stress underlies common variation in metabolic traits.	Nature	2020
31402314	Leigh Syndrome Mouse Model Can Be Rescued by Interventions that Normalize Brain Hyperoxia, but Not HIF Activation.	Cell Metab	2019
30520688	Impaired hypoxic pulmonary vasoconstriction in a mouse model of Leigh syndrome.	Am J Physiol Lung Cell Mol Physiol	2019
31042465	Exploring the InÂ Vivo Role of the Mitochondrial Calcium Uniporter in Brown Fat Bioenergetics.	Cell Rep	2019
29073106	Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter.	Proc Natl Acad Sci U S A	2017
28483998	Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome.	Proc Natl Acad Sci U S A	2017
27307216	Mitochondrial dysfunction remodels one-carbon metabolism in human cells.	Elife	2016
26917594	Hypoxia as a therapy for mitochondrial disease.	Science	2016
24231807	EMRE is an essential component of the mitochondrial calcium uniporter complex.	Science	2013
21685886	Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter.	Nature	2011
21907147	Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.	Cell Metab	2011
20080599	A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells.	Proc Natl Acad Sci U S A	2010
20818383	High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.	Nat Genet	2010
16582907	Systematic identification of human mitochondrial disease genes through integrative genomics.	Nat Genet	2006
16807246	Syndecan-1 expression in epithelial cells is induced by transforming growth factor beta through a PKA-dependent pathway.	Journal of Biological Chemistry	2006
16669614	Insulin promotes shedding of syndecan ectodomains from 3T3-L1 adipocytes: a proposed mechanism for stabilization of extracellular lipoprotein lipase.	Biochemistry	2006
15226297	Chondroitin sulfate chains on syndecan-1 and syndecan-4 from normal murine mammary gland epithelial cells are structurally and functionally distinct and cooperate with heparan sulfate chains to bind growth factors. A novel function to control binding of m	Journal of Biological Chemistry	2004
12571251	Syndecan-1 and -4 synthesized simultaneously by mouse mammary gland epithelial cells bear heparan sulfate chains that are apparently structurally indistinguishable.	Journal of Biological Chemistry	2003
12414997	Defects in keratinocyte activation during wound healing in the syndecan-1-deficient mouse.	Journal of Cell Science	2002
11461706	Transgenic expression of syndecan-1 uncovers a physiological control of feeding behavior by syndecan-3.	Cell	2001
10652286	Syndecan-1 shedding is enhanced by LasA, a secreted virulence factor of Pseudomonas aeruginosa.	Journal of Biological Chemistry	2000
7959737	Mapping of the syndecan genes in the mouse: linkage with members of the myc gene family.	Genomics	1994
7812048	Members of the syndecan family of heparan sulfate proteoglycans are expressed in distinct cell-, tissue-, and development-specific patterns.	Molecular Biology of the Cell	1994
8496192	Organization and promoter activity of the mouse syndecan-1 gene.	Journal of Biological Chemistry	1993