J. Issartel

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A mutation located at the 5' splice junction sequence of intron 3 in the p67phox gene causes the lack of p67phox mRNA in a patient with chronic granulomatous disease.

F. Morel, L. C. Tanugi-Cholley, J. Issartel, 1995, Blood.

Activation of Escherichia coli prohaemolysin to the mature toxin by acyl carrier protein-dependent fatty acylation

J. Issartel, V. Koronakis, C. Hughes, 1991, Nature.

The transcriptomic response of mixed neuron-glial cell cultures to 1,25-dihydroxyvitamin d3 includes genes limiting the progression of neurodegenerative diseases.

D. Wion, F. Berger, J. Brocard, 2013, Journal of Alzheimer's disease : JAD.

Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductase.

V. Procaccio, J. Lunardi, P. Martinez, 1998, Gene.

Ethical issues in brain nanomedicine

P. Caillat, D. Wion, A. Bouamrani, 2005 .

Possible Biohazard Risk from Infectious Tissue and Culture Cells Preserved with RNAlater

E. Brambilla, A. Bouamrani, J. Issartel, 2007 .

Hypoxia-induced expression of VE-cadherin and filamin B in glioma cell cultures and pseudopalisade structures

Jean-Paul Issartel, François Berger, Emmanuel Garcion, 2013, Journal of Neuro-Oncology.

[Oxygen tension and cancer-cell culture: half a century of artifacts?].

D. Wion, F. Berger, J. Issartel, 2008, Medecine sciences : M/S.

Inhibition of H+-transporting ATPase by formation of a tight nucleoside diphosphate-fluoroaluminate complex at the catalytic site.

J. Garin, J. Issartel, J. Lunardi, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Additional clues for a protective role of vitamin D in neurodegenerative diseases: 1,25-dihydroxyvitamin D3 triggers an anti-inflammatory response in brain pericytes.

D. Wion, F. Berger, J. Issartel, 2014, Journal of Alzheimer's disease : JAD.

The heterogeneity of meningioma revealed by multiparameter analysis: infiltrative and non-infiltrative clinical phenotypes.

D. Wion, C. Salon, A. Bouamrani, 2011, International journal of oncology.

Activation of Escherichia coli prohemolysin to the membrane-targetted toxin by HlyC-directed ACP-dependent fatty acylation.

K. Hardie, J. Issartel, P. Stanley, 1992, FEMS microbiology immunology.

Two EPR-detectable [4Fe-4S] clusters, N2a and N2b, are bound to the NuoI (TYKY) subunit of NADH:ubiquinone oxidoreductase (Complex I) from Rhodobacter capsulatus.

J. Lunardi, J. Issartel, M. Chevallet, 2003, Biochimica et biophysica acta.

In vitro activation of Escherichia coli prohaemolysin to the mature membrane‐targeted toxin requires HlyC and a low molecular‐weight cytosolic polypeptide

K. Hardie, J. Issartel, V. Koronakis, 1991, Molecular microbiology.

cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I.

M. Mattei, V. Procaccio, J. Lunardi, 1997, Biochimica et biophysica acta.

The nuoM arg368his mutation in NADH:ubiquinone oxidoreductase from Rhodobacter capsulatus: a model for the human nd4-11778 mtDNA mutation associated with Leber's hereditary optic neuropathy.

J. Lunardi, J. Issartel, E. Darrouzet, 1998, Biochimica et biophysica acta.

The NuoI subunit of the Rhodobacter capsulatus respiratory Complex I (equivalent to the bovine TYKY subunit) is required for proper assembly of the membraneous and peripheral domains of the enzyme.

J. Lunardi, J. Issartel, M. Chevallet, 1997, European journal of biochemistry.

Immuno‐purification of a dimeric subcomplex of the respiratory NAHD‐CoQ reductase of Rhodobacter capsulatus equivalent to the FP fraction of the mitochondrial complex I

A. Chapel, J. Lunardi, S. Kieffer, 1997, FEBS letters.

Inhibition of c-Jun N-terminal kinase by SP600125: a cDNA microarray analysis.

F. Berger, D. Seigneurin, J. Issartel, 2010, Cancer genomics & proteomics.

Extracellular vesicles from myelodysplastic mesenchymal stromal cells induce DNA damage and mutagenesis of hematopoietic stem cells through miRNA transfer

P. Hainaut, J. Deleuze, J. Thevenon, 2020, Leukemia.

Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy

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

Synthesis and properties of azidonitrophenyl pyrophosphate, a photoaffinity probe of the nucleotide binding sites of mitochondrial F1-ATPase.

J. Garin, J. Issartel, P. Vignais, 1989, Biochemistry.

Large functional range of steady-state levels of nuclear and mitochondrial transcripts coding for the subunits of the human mitochondrial OXPHOS system.

B. Mousson de Camaret, J. Issartel, R. Beugnot, 2002, Genome research.

[70] Modifiers of F1-ATPases and associated peptides

J. Lunardi, G. Klein, M. Satre, 1986 .

Photolabeling of the phosphate binding site of mitochondrial F1-ATPase by [32P]azidonitrophenyl phosphate. Identification of the photolabeled amino acid residues.

J. Garin, J. Lunardi, J. Issartel, 1989, Biochemistry.

Identification of amino acid residues photolabeled with 2-azido[alpha-32P]adenosine diphosphate in the beta subunit of beef heart mitochondrial F1-ATPase.

J. Garin, J. Issartel, J. Lunardi, 1986, Biochemistry.

The complex I from Rhodobacter capsulatus.

J. Lunardi, J. Issartel, M. Chevallet, 1998, Biochimica et biophysica acta.

Interactions between the oligomycin sensitivity conferring protein (OSCP) and beef heart mitochondrial F1-ATPase. 2. Identification of the interacting F1 subunits by cross-linking.

J. Issartel, J. Lunardi, P. Vignais, 1985, Biochemistry.

Interactions between the oligomycin sensitivity conferring protein (OSCP) and beef heart mitochondrial F1-ATPase. 1. Study of the binding parameters with a chemically radiolabeled OSCP.

J. Lunardi, M. Satre, J. Issartel, 1985, Biochemistry.

Fluoride, beryllium and ADP combine as a ternary complex in aqueous solution as revealed by a multinuclear NMR study

J. Issartel, J. Girardet, A. Dupuis, 2004, European Biophysics Journal.

MicroRNAs: molecular features and role in cancer.

F. Berger, J. Issartel, Audrey Guttin, 2012, Frontiers in bioscience.

Chemical modification of F1-ATPase by dicyclohexylcarbodiimide: application to analysis of the stoichiometry of subunits in Escherichia coli F1.

M. Satre, J. Issartel, P. Vignais, 1982, Biochemistry.

Direct identification of the fluoroaluminate and fluoroberyllate species responsible for inhibition of the mitochondrial F1‐ATPase

J. Issartel, P. Vignais, A. Dupuis, 1989 .

Synthesis and enzymatic incorporation of morpholino thymidine-5′-triphosphate in DNA fragments

Sylvie Sauvaigo, Jean-Paul Issartel, J. Issartel, 1999 .

MicroRNA and Target Protein Patterns Reveal Physiopathological Features of Glioma Subtypes

C. Godfraind, D. Wion, C. Salon, 2011, PloS one.

Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin.

C. Remacle, P. Cardol, G. Hofhaus, 2004, The Biochemical journal.

MicroRNA-Based Drugs for Brain Tumors.

C. Loussouarn, P. Baril, M. Garnett, 2018, Trends in cancer.

Brain mesenchymal stem cells: The other stem cells of the brain?

D. Wion, F. Berger, F. Appaix, 2014, World journal of stem cells.

PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice

N. Thierry-Mieg, B. Conne, P. Ray, 2018, EMBO Molecular Medicine.

Mapping to 1q23 of the human gene (NDUFS2) encoding the 49-kDa subunit of the mitochondrial respiratory Complex I and immunodetection of the mature protein in mitochondria

V. Procaccio, J. Lunardi, P. Soularue, 1998, Mammalian Genome.

Towards a new standardized method for circulating miRNAs profiling in clinical studies: Interest of the exogenous normalization to improve miRNA signature accuracy

S. Lheureux, B. Clarisse, F. Joly, 2016, Molecular oncology.

Aurovertin binding sites on beef heart mitochondrial F1-ATPase. Study with [14C]aurovertin D of the binding stoichiometry and of the interaction between aurovertin and the natural ATPase inhibitor for binding to F1.

G. Klein, M. Satre, J. Issartel, 1983, Biochemistry.

Binding of [14C]aurovertin D to Escherichia coli F1-ATPase and the isolated .beta. subunit. Correlation with inhibition of the ATPase activity

G. Klein, M. Satre, J. Issartel, 1983 .

Quantification of mitochondrial DNA deletion, depletion, and overreplication: application to diagnosis.

B. Chabi, B. Mousson de Camaret, J. Issartel, 2003, Clinical chemistry.

Is pyrophosphate an analog of adenosine diphosphate for beef heart mitochondrial F1-ATPase.

J. Issartel, J. Lunardi, P. Vignais, 1987, The Journal of biological chemistry.

Does pyrophosphate bind to the catalytic sites of mitochondrial F1-ATPase?

J. Issartel, J. Lunardi, P. Vignais, 1992, Biochemistry.

Direct-tissue SELDI-TOF mass spectrometry analysis: a new application for clinical proteomics.

A. Benabid, E. Brambilla, A. Bouamrani, 2006, Clinical chemistry.

Increased Phosphorylation of Vimentin in Noninfiltrative Meningiomas

M. Cubizolles, D. Wion, A. Bouamrani, 2010, PloS one.

Translation of the ecological trap concept to glioma therapy: the cancer cell trap concept.

D. Wion, F. Berger, F. Appaix, 2013, Future oncology.

The 49‐kDa subunit of NADH‐ubiquinone oxidoreductase (Complex I) is involved in the binding of piericidin and rotenone, two quinone‐related inhibitors

J. Lunardi, J. Issartel, E. Darrouzet, 1998, FEBS letters.

Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial Complex I: genomic organization and expression

P. Lescuyer, H. Smeets, V. Procaccio, 2000, Mammalian Genome.

Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.

H. Smeets, V. Procaccio, G. Putet, 1999, The Journal of clinical investigation.

Structure, Function and Pathology of Complex I

V. Procaccio, J. Lunardi, J. Issartel, 1999 .

The ATP synthase (F0−F1) complex in oxidative phosphorylation

J. Garin, J. Lunardi, J. Issartel, 1992, Experientia.

Network-Based Integration of Multi-Omics Data Identifies the Determinants of miR-491-5p Effects

E. Barillot, L. Martignetti, D. Loew, 2021, Cancers.

Atomic structure and composition of the 2 × N reconstruction of the Ge wetting layer on Si(001) investigated by surface x-ray diffraction

G. Renaud, Â. Malachias, J. Issartel, 2011 .

Novel methods of powder preparation and ceramic forming for improving reliability of multilayer ceramic actuators

William J. Dawson, Scott L. Swartz, Craig D. Near, 1993, Smart Structures.

Computational identification of transcriptionally co-regulated genes, validation with the four ANT isoform genes

J. Issartel, Audrey Guttin, G. Stepien, 2012, BMC Genomics.

Comparative proteomic profiles of Aspergillus fumigatus and Aspergillus lentulus strains by surface-enhanced laser desorption ionization time-of-flight mass spectrometry (SELDI-TOF-MS)

R. Grillot, F. Berger, J. Issartel, 2011, BMC Microbiology.

Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out mice

P. Ray, C. Coutton, C. Arnoult, 2013, Basic and Clinical Andrology.

Analytic Hamiltonian Systems, the Vicinity of a Periodic Solution

C. Marchal, J. Issartel, 1995 .

Characterization of exchangeable and nonexchangeable bound adenine nucleotides in F1-ATPase from Escherichia coli.

J. Issartel, J. Lunardi, P. Vignais, 1986, The Journal of biological chemistry.

Fluoroaluminum and fluoroberyllium nucleoside diphosphate complexes as probes of the enzymatic mechanism of the mitochondrial F1-ATPase.

J. Issartel, J. Lunardi, P. Vignais, 1991, Biochemistry.

Translation of the ecological trap concept to glioma therapy: the cancer cell trap concept.

D. Wion, F. Berger, F. Appaix, 2013, Future oncology.

The transcriptomic response of mixed neuron-glial cell cultures to 1,25-dihydroxyvitamin d3 includes genes limiting the progression of neurodegenerative diseases.

D. Wion, F. Berger, J. Brocard, 2013, Journal of Alzheimer's disease : JAD.

Fluoroaluminum and Fluoroberyllium Complexes as Probes of the Catalytic Sites of Mitochondrial F1-ATPase

J. Garin, J. Lunardi, J. Issartel, 1992 .

Mapping of nucleotide-depleted mitochondrial F1-ATPase with 2-azido-[alpha-32P]adenosine diphosphate. Evidence for two nucleotide binding sites in the beta subunit.

J. Garin, J. Issartel, J. Lunardi, 1987, The Journal of biological chemistry.

Identification of five Rhodobacter capsulatus genes encoding the equivalent of ND subunits of the mitochondrial NADH-ubiquinone oxidoreductase.

V. Procaccio, J. Lunardi, J. Issartel, 1995, Gene.