Publikationen in Zusammenarbeit mit Forschern von French Institute of Health and Medical Research (18)

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2020

  1. Five insights from the Global Burden of Disease Study 2019

    The Lancet, Vol. 396, Núm. 10258, pp. 1135-1159

  2. Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019

    The Lancet, Vol. 396, Núm. 10258, pp. 1160-1203

  3. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019

    The Lancet, Vol. 396, Núm. 10258, pp. 1204-1222

  4. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019

    The Lancet, Vol. 396, Núm. 10258, pp. 1223-1249

  5. Semi-mechanistic PK/PD modelling of combined polymyxin B and minocycline against a polymyxin-resistant strain of Acinetobacter baumannii

    Clinical Microbiology and Infection, Vol. 26, Núm. 9, pp. 1254.e9-1254.e15

2018

  1. Heterogeneity of spontaneous DNA replication errors in single isogenic Escherichia coli cells

    Science Advances, Vol. 4, Núm. 6

2017

  1. The SOS and RpoS regulons contribute to bacterial cell robustness to genotoxic stress by synergistically regulating DNA polymerase pol II

    Genetics, Vol. 206, Núm. 3, pp. 1349-1360

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

  3. Stress-Induced Depressive Behaviors Require a Functional NLRP3 Inflammasome

    Molecular Neurobiology, Vol. 53, Núm. 7, pp. 4874-4882

  4. The COQ2 genotype predicts the severity of Coenzyme Q10 deficiency

    Human Molecular Genetics, Vol. 25, Núm. 19, pp. 4256-4265

2012

  1. Guidelines for the use and interpretation of assays for monitoring autophagy

    Autophagy, Vol. 8, Núm. 4, pp. 445-544

2011

  1. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

    Journal of Clinical Investigation, Vol. 121, Núm. 5, pp. 2013-2024

2009

  1. Expression of the Ciona intestinalis Alternative Oxidase (AOX) in Drosophila Complements Defects in Mitochondrial Oxidative Phosphorylation

    Cell Metabolism, Vol. 9, Núm. 5, pp. 449-460

2006

  1. Resuscitation of severe but brief haemorrhagic shock with PFC in rabbits restores skeletal muscle oxygen delivery and does not alter skeletal muscle metabolism

    Resuscitation, Vol. 70, Núm. 1, pp. 124-132

2005

  1. Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition

    Neurology, Vol. 65, Núm. 4, pp. 606-608

2003

  1. Analysis of a key regulatory region upstream of the Myf5 gene reveals multiple phases of myogenesis, orchestrated at each site by a combination of elements dispersed throughout the locus

    Development, Vol. 130, Núm. 15, pp. 3415-3426