S. Lebon

发表

Immediate remote ischemic postconditioning after hypoxia ischemia in piglets protects cerebral white matter but not grey matter

X. Golay, P. Gressens, K. Broad, 2015, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain.

E. Petretto, W. Birchmeier, D. Rowitch, 2019, Brain : a journal of neurology.

Molecular diagnostics of mitochondrial disorders.

A. Munnich, A. Rötig, E. Sarzi, 2004, Biochimica et biophysica acta.

Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains

P. Gressens, S. Auvin, B. Desnous, 2016, Journal of Neuroinflammation.

Role of microglia in a mouse model of paediatric traumatic brain injury

C. Zuiani, P. Gressens, H. Hagberg, 2017, Brain, Behavior, and Immunity.

Trans-Modulation of the Somatostatin Type 2A Receptor Trafficking by Insulin-Regulated Aminopeptidase Decreases Limbic Seizures

G. Collingridge, P. Gressens, S. Peineau, 2015, The Journal of Neuroscience.

Mitochondrial Complex I Deficiency in Humans

P. Bénit, P. Rustin, A. Rötig, 2004 .

A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia

A. Munnich, M. Brown, V. Procaccio, 2007, American journal of medical genetics. Part A.

Respiratory-chain diseases related to complex III deficiency.

P. Bénit, P. Rustin, S. Lebon, 2009, Biochimica et biophysica acta.

A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome.

A. Munnich, A. Rötig, J. Steffann, 2007, Molecular genetics and metabolism.

A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome.

A. Munnich, A. Rötig, D. Rodriguez, 2007, Molecular genetics and metabolism.

Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndrome

P. Verroust, F. Emma, E. Christensen, 2013, BMC Medical Genetics.

Neuroprotective Effects of Dexmedetomidine against Glutamate Agonist-induced Neuronal Cell Death Are Related to Increased Astrocyte Brain-derived Neurotrophic Factor Expression

P. Gressens, J. Mantz, L. Schwendimann, 2013, Anesthesiology.

High homocysteine induces betaine depletion

H. Blom, A. Imbard, W. Kruger, 2015, Bioscience reports.

Targeting the brain 5-HT7 receptor to prevent hypomyelination in a rodent model of perinatal white matter injuries

T. Vitalis, P. Gressens, Juliette van Steenwinckel, 2022, Journal of Neural Transmission.

A Novel RAB33B Mutation in Smith–McCort Dysplasia

P. Gressens, V. El Ghouzzi, L. Graul-Neumann, 2013, Human mutation.

Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development

A. Munnich, A. Rötig, A. Benachi, 2006, Journal of Medical Genetics.

Stiripentol exhibits higher anticonvulsant properties in the immature than in the mature rat brain

P. Gressens, S. Auvin, B. Desnous, 2013, Epilepsia.

How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption?

M. Schiff, S. Lebon, O. Fenneteau, 2012, Molecular genetics and metabolism.

Characterization of phenotype markers and neuronotoxic potential of polarised primary microglia in vitro

P. Gressens, H. Hagberg, B. Fleiss, 2013, Brain, Behavior, and Immunity.

VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling.

C. Verney, P. Gressens, A. Verloes, 2011, The Journal of clinical investigation.

A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis

P. Rustin, A. Legrand, J. Saudubray, 2003, Human Genetics.

Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes.

P. Bénit, G. Gyapay, J. Weissenbach, 2002, Human molecular genetics.

ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53

M. Vignuzzi, P. Gressens, F. Di Cunto, 2016, Cell Death and Disease.

ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53

M. Vignuzzi, P. Gressens, F. Di Cunto, 2016, Cell Death and Disease.

Vulnerability of white matter towards antenatal hypoxia is linked to a species-dependent regulation of glutamate receptor subunits

P. Gressens, P. Leroux, O. Baud, 2008, Proceedings of the National Academy of Sciences.

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

P. Bénit, A. Munnich, P. Rustin, 2004, Journal of Medical Genetics.

ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects.

K. Shirahige, T. Akiyama, P. Gressens, 2016, American journal of human genetics.

Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies.

P. Rustin, Malgorzata Rak, L. Aubry, 2013, Human molecular genetics.

Fatal manifestation of a de novo ND5 mutation: Insights into the pathogenetic mechanisms of mtDNA ND5 gene defects.

T. Schurr, S. Zhadanov, S. Lebon, 2007, Mitochondrion.

Loss of the Wnt/β-catenin pathway in microglia of the developing brain drives pro-inflammatory activation leading to white matter injury

E. Petretto, W. Birchmeier, D. Rowitch, 2018, bioRxiv.

Cell Metabolic Alterations due to Mcph1 Mutation in Microcephaly.

P. Bénit, J. Oury, P. Gressens, 2020, Cell reports.

The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation.

P. Rustin, A. Rötig, G. Choukroun, 2003, Journal of the American Society of Nephrology : JASN.

Myelination induction by a histamine H3 receptor antagonist in a mouse model of preterm white matter injury

B. Matrot, A. Edwards, P. Gressens, 2018, Brain, Behavior, and Immunity.

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

P. Bénit, A. Munnich, L. Hertz-Pannier, 2003, Journal of medical genetics.

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

P. Bénit, A. Munnich, L. Hertz-Pannier, 2003, Journal of medical genetics.

Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome

P. Bénit, A. Munnich, P. Rustin, 2003, Human Genetics.

Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblasts.

P. Bénit, A. Munnich, P. Rustin, 2003, Biochemical and biophysical research communications.

Liver and brain differential expression of one-carbon metabolism genes during ontogenesis

H. Blom, P. Gressens, A. Imbard, 2021, Scientific Reports.

The Anti-Inflammatory Effects of the Small Molecule Pifithrin-µ on BV2 Microglia

P. Gressens, C. Thornton, H. Hagberg, 2015, Developmental Neuroscience.

Contribution of mast cells to injury mechanisms in a mouse model of pediatric traumatic brain injury

P. Gressens, S. Rasika, B. Fleiss, 2016, Journal of neuroscience research.

Genetic inhibition of caspase‐2 reduces hypoxic‐ischemic and excitotoxic neonatal brain injury

P. Gressens, H. Hagberg, Xiaoyang Wang, 2011, Annals of neurology.

Involvement of the synapse‐specific zinc transporter ZnT3 in cadmium‐induced hippocampal neurotoxicity

P. Gressens, Juliette van Steenwinckel, Tifenn le Charpentier, 2019, Journal of cellular physiology.

Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR.

A. Munnich, N. Frydman, R. Frydman, 2005, Molecular genetics and metabolism.

Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency.

E. Holme, P. Rustin, N. Darín, 2003, Neuropediatrics.

miR‐146b Protects the Perinatal Brain against Microglia‐Induced Hypomyelination

P. Gressens, B. Fleiss, Juliette van Steenwinckel, 2021, Annals of neurology.

A new lysosomal storage disorder resembling Morquio syndrome in sibs.

B. Ilharreborde, A. Verloes, V. El Ghouzzi, 2012, European journal of medical genetics.

VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling.

C. Verney, P. Gressens, A. Verloes, 2011, The Journal of clinical investigation.

Myelination induction by a histamine H3 receptor antagonist in a mouse model of preterm white matter injury

B. Matrot, A. Edwards, B. Fleiss, 2018, Brain, Behavior, and Immunity.

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

L. Hertz-Pannier, P. Rustin, A. Rötig, 2003, Journal of medical genetics.

G protein-coupled receptor 17 is regulated by WNT pathway during oligodendrocyte precursor cell differentiation

Anne-Laure Schang, S. Mani, S. Lebon, 2023, Neurobiology of Disease.