Citation Impact
Citing Papers
EglN2 associates with the NRF 1‐ PGC 1α complex and controls mitochondrial function in breast cancer
2015 StandoutNobel
Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism
2024 StandoutNobel
The epidemiology of severe sepsis in England, Wales and Northern Ireland, 1996 to 2004: secondary analysis of a high quality clinical database, the ICNARC Case Mix Programme Database
2006
Imaging beyond the proteome
2012 StandoutNobel
Homozygous acute intermittent porphyria: compound heterozygosity for adjacent base transitions in the same codon of the porphobilinogen deaminase gene
1992
AMPK: guardian of metabolism and mitochondrial homeostasis
2017 Standout
The mitochondrial UPR: mechanisms, physiological functions and implications in ageing
2017
Melanin Pigmentation in Mammalian Skin and Its Hormonal Regulation
2004 Standout
Energy metabolism in tumor cells
2007
The genetics of ageing
2010 StandoutNature
Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene
2006
The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease
2015 Standout
Analysis of the glucocerebrosidase gene and mutation profile in 144 Italian gaucher patients
2002
An overview of mortality and sequelae of preterm birth from infancy to adulthood
2008 Standout
A New Gene–Pseudogene Fusion Allele Due to a Recombination in Intron 2 of the Glucocerebrosidase Gene Causes Gaucher Disease
2000
Porphyrias
2010 Standout
Whither Ribosome Structure and Dynamics Research? (A Perspective)
2016 StandoutNobel
Severe Sepsis and Septic Shock
2013 Standout
A new role for the von Hippel-Lindau tumor suppressor protein: stimulation of mitochondrial oxidative phosphorylation complex biogenesis
2004
Heat Shock Protein A12B Protects Vascular Endothelial Cells Against Sepsis-Induced Acute Lung Injury in Mice
2017 Standout
Are mitochondria critical in the pathogenesis of Alzheimer's disease?
2005
HIF-1 Inhibits Mitochondrial Biogenesis and Cellular Respiration in VHL-Deficient Renal Cell Carcinoma by Repression of C-MYC Activity
2007 StandoutNobel
Assembly of mitochondrial complex I and defects in disease
2008
Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride
2006
Mitochondria: In Sickness and in Health
2012 Standout
Mechanisms of NAFLD development and therapeutic strategies
2018 Standout
High efficiency of ROS production by glycerophosphate dehydrogenase in mammalian mitochondria
2008
Proteolytic Cleavage of Opa1 Stimulates Mitochondrial Inner Membrane Fusion and Couples Fusion to Oxidative Phosphorylation
2014
Regulation of cancer cell metabolism
2011 Standout
Translation of nonSTOP mRNA is repressed post‐initiation in mammalian cells
2007
Charting the travels of copper in eukaryotes from yeast to mammals
2012
Sepsis and septic shock
2018 Standout
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
A Targetable Fluorescent Sensor Reveals That Copper-Deficient SCO1 and SCO2 Patient Cells Prioritize Mitochondrial Copper Homeostasis
2011
Hydrocortisone Therapy for Patients with Septic Shock
2008 Standout
Alzheimer's disease
2006 Standout
Mitochondrial Membrane Permeabilization in Cell Death
2007 Standout
Incidence of sepsis in hospitalized patients
2006
Mitochondrial disorders caused by mutations in respiratory chain assembly factors
2011
HIF-1 Regulates Cytochrome Oxidase Subunits to Optimize Efficiency of Respiration in Hypoxic Cells
2007 StandoutNobel
Oxidative stress in developmental brain disorders
2009
Mitochondria as multifaceted regulators of cell death
2019 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Electron transfer and energy transduction in the terminal part of the respiratory chain — Lessons from bacterial model systems
2009
Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease Evidence for a disease specific abnormality of the myocardial interstitium
2003
AIF deficiency compromises oxidative phosphorylation
2004
International Study of the Prevalence and Outcomes of Infection in Intensive Care Units
2009 Standout
Rapid increase in hospitalization and mortality rates for severe sepsis in the United States: A trend analysis from 1993 to 2003*
2007 Standout
Two distinct forms of minor neurological dysfunction: perspectives emerging from a review of data of the Groningen Perinatal Project
2002
Increased longevity and refractoriness to Ca2+-dependent neurodegeneration in Surf1 knockout mice
2007
Epidemiologic Trend of Severe Sepsis in Taiwan From 1997 Through 2006
2010
Mitochondrial Diseases: Hope for the Future
2020
Selective Inhibition of Hypoxia-Inducible Factor (HIF) Prolyl-Hydroxylase 1 Mediates Neuroprotection against Normoxic Oxidative Death via HIF- and CREB-Independent Pathways
2009 StandoutNobel
A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase
2020
The complete structure of the large subunit of the mammalian mitochondrial ribosome
2014 Nature
Assembly of nuclear DNA‐encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria
2009
What is new in CDG?
2017
Assessment of Clinical Criteria for Sepsis
2016 Standout
The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3)
2016 Standout
Nanozymes: Classification, Catalytic Mechanisms, Activity Regulation, and Applications
2019 Standout
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
1995 Standout
Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondria
2016
Meeting Report: Exploiting the Tumor Microenvironment for Therapeutics
2006 StandoutNobel
The Protein Kinase Complement of the Human Genome
2002 StandoutScience
Worldwide Occurrences of Arsenic in Ground Water
2002 StandoutScience
Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients With Mitochondrial Disease
2004
Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model
2013
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
The epidemiology of sepsis in a Brazilian teaching hospital
2010
Aggregation-Induced Emission: Together We Shine, United We Soar!
2015 Standout
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
The epidemiology of sepsis in a Brazilian teaching hospital
2010
Sepsis syndrome in Croatian intensive care units: piloting a national comparative clinical database.
2006
The cutaneous porphyrias: a review
1999
Review: Mitochondrial medicine--cardiomyopathy caused by defective oxidative phosphorylation.
2003
Fibroblast Growth Factor 21—Metabolic Role in Mice and Men
2017
The Caenorhabditis elegans ARIP-4 DNA helicase couples mitochondrial surveillance to immune, detoxification, and antiviral pathways
2022 StandoutNobel
Fluorescent Sensors for Measuring Metal Ions in Living Systems
2014 Standout
Arsenic in Ground Water of the United States: Occurrence and Geochemistry
2000
The Ecology of Arsenic
2003 StandoutScience
Copper induces cell death by targeting lipoylated TCA cycle proteins
2022 StandoutScience
Two distinct forms of minor neurological dysfunction: perspectives emerging from a review of data of the Groningen Perinatal Project
2002
Fabry Disease, an Under-Recognized Multisystemic Disorder: Expert Recommendations for Diagnosis, Management, and Enzyme Replacement Therapy
2003
Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet
2011 StandoutNobel
Activation of mitochondrial protease OMA1 by Bax and Bak promotes cytochrome c release during apoptosis
2014
Copper Metallochaperones
2010
Investigating the functional link between TMEM165 and SPCA1
2019 StandoutNobel
Developing a New Definition and Assessing New Clinical Criteria for Septic Shock
2016 Standout
Regulation of mRNA Translation and Stability by microRNAs
2010 Standout
Design Strategies for Water-Soluble Small Molecular Chromogenic and Fluorogenic Probes
2013 Standout
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
2009 StandoutScience
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel
Proton-Coupled Electron Transfer
2012 Standout
Works of J Zeman being referenced
[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome].
1999
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
2007
Knockdown of Human Oxa1l Impairs the Biogenesis of F1Fo-ATP Synthase and NADH:Ubiquinone Oxidoreductase
2007
Specific Properties of Heavy Fraction of Mitochondria from Human-term Placenta – Glycerophosphate-dependent Hydrogen Peroxide Production
2005
The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues
2008
A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis
2001
Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome
2003
Decreased affinity for oxygen of cytochrome-c oxidase in Leigh syndrome caused by SURF1 mutations
2004
Loss of function of Sco1 and its interaction with cytochrome c oxidase
2009
Epidemiology of Severe Sepsis in Intensive Care Units in the Slovak Republic
2005
Monoamine Neurotransmitters and Metabolites in the Cerebrospinal Fluid following Perinatal Asphyxia
1995
SURF1 missense mutations promote a mild Leigh phenotype
2009
Assembly factors and ATP-dependent proteases in cytochrome c oxidase biogenesis
2010
Biogenesis of eukaryotic cytochrome c oxidase
2006
New insights in cardiac structural changes in patients with Fabry’s disease
2000
Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation
2014
Genetic defects of cytochrome c oxidase assembly
2004
Increased erythrocyte protoporphyrin in homozygous variegate porphyria.
1985
Analysis of the β-Glucocerebrosidase Gene in Czech and Slovak Gaucher Patients: Mutation Profile and Description of Six Novel Mutant Alleles
1999
Outcome measures for children with mitochondrial disease: consensus recommendations for future studies from a Delphi‐based international workshop
2018
Acute hyperammonaemic encephalopathy in a female newborn caused by a novel, de novo mutation in the ornithine transcarbamylase gene
2004
Vascular presentation of cystathionine beta‐synthase deficiency in adulthood
2010
Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1
2005
The Clinical Spectrum of Mitochondrial Disease in 75 Pediatric Patients
2003
Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206
2004
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation
2012
Oxidation of arsenopyrite by Thiobacillus ferrooxidans detected by a mineral electrode
1995
Clinical manifestation of mitochondrial diseases.
2016