M. Corral‐Debrinski

发表

Pse1/Kap121‐dependent nuclear localization of the major yeast multidrug resistance (MDR) transcription factor Pdr1

C. Jacq, M Corral-Debrinski, A. Delahodde, 2001, Molecular microbiology.

Cell Contact-Mediated Regulation of Hepatocyte Differentiation/Proliferation: Role of LRP(s)

C. Guguen-Guillouzo, P. Loyer, S. Cariou, 1994 .

mRNA specific subcellular localization represents a crucial step for fine-tuning of gene expression in mammalian cells.

M. Corral‐Debrinski, 2007, Biochimica et biophysica acta.

Neuroglobin and prion cellular localization: investigation of a potential interaction.

D. Hamdane, L. Kiger, M. Marden, 2009, Journal of molecular biology.

Interactions of Human Hepatocytes with Hepatitis B Virus

C. Guguen-Guillouzo, P. Gripon, J. Cillard, 1994 .

Coevolution predicts direct interactions between mtDNA-encoded and nDNA-encoded subunits of oxidative phosphorylation complex i.

D. Frishman, A. Fuchs, D. Mishmar, 2010, Journal of molecular biology.

Neuroglobin effectively halts vision loss in Harlequin mice at an advanced stage of optic nerve degeneration

Christophe Lechauve, T. Debeir, M. Corral‐Debrinski, 2021, Neurobiology of Disease.

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

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

Drug development for mitochondrial disease: recent progress, current challenges, and future prospects

P. Bénit, P. Rustin, M. Schiff, 2016 .

The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes.

P. Bénit, J. Sahel, P. Rustin, 2008, Biochimica et biophysica acta.

Nuclear expression of mitochondrial ND4 leads to the protein assembling in complex I and prevents optic atrophy and visual loss

J. Sahel, Christophe Lechauve, M. Corral‐Debrinski, 2015, Molecular therapy. Methods & clinical development.

Downregulation of apoptosis-inducing factor in Harlequin mice induces progressive and severe optic atrophy which is durably prevented by AAV2-AIF1 gene therapy.

P. Bénit, J. Sahel, P. Rustin, 2012, Brain : a journal of neurology.

Focus on optic neuropathies due to mitochondrial dysfunction: molecular bases and putative therapies

J. Sahel, M. Corral‐Debrinski, M. Corral-Debrinski, 2008 .

Long‐term productive episomal hepatitis B virus replication in primary cultures of adult human hepatocytes infected in vitro

C. Guguen-Guillouzo, P. Gripon, M. Corral‐Debrinski, 1996, Journal of viral hepatitis.

mRNA localization to the mitochondrial surface allows the efficient translocation inside the organelle of a nuclear recoded ATP6 protein.

J. Sahel, V. Forster, C. Bonnet, 2006, RNA.

Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.

D. Wallace, M. Lott, J. Shoffner, 1991, JAMA.

Mitochondrial medicine: to a new era of gene therapy for mitochondrial DNA mutations

J. Sahel, M. Corral‐Debrinski, Hélène Cwerman-Thibault, 2011, Journal of Inherited Metabolic Disease.

Yeast Functional Analysis: Identification of Two Essential Genes Involved in ER to Golgi Trafficking

R. Haguenauer‐Tsapis, T. Munder, S. Le Panse, 2003, Traffic.

In Saccharomyces cerevisiae, ATP2 mRNA sorting to the vicinity of mitochondria is essential for respiratory function

C. Jacq, C. Blugeon, A. Margeot, 2002, The EMBO journal.

In Yeast, the 3′ Untranslated Region or the Presequence ofATM1 Is Required for the Exclusive Localization of Its mRNA to the Vicinity of Mitochondria

C. Jacq, C. Blugeon, M. Corral‐Debrinski, 2000, Molecular and Cellular Biology.

Overexpression of yeast karyopherin Pse1p/Kap121p stimulates the mitochondrial import of hydrophobic proteins in vivo

C. Jacq, M. Claros, V. Doye, 1999, Molecular microbiology.

Genome‐wide analysis of mRNAs targeted to yeast mitochondria

Antoine Margeot, Claude Jacq, Philippe Marc, 2002, EMBO reports.

Gene therapy for mitochondrial diseases: Leber Hereditary Optic Neuropathy as the first candidate for a clinical trial.

J. Sahel, M. Corral‐Debrinski, S. Augustin, 2014, Comptes rendus biologies.

Differential proto-oncogene mRNA induction from rats treated with peroxisome proliferators.

N. Latruffe, Y. Lone, M. Corral‐Debrinski, 1990, Biochemical and biophysical research communications.

Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients

M. Beal, D. Wallace, B. Graham, 1995, Neurology.

Neuroglobin involvement in visual pathways through the optic nerve.

J. Sahel, Christophe Lechauve, M. Corral‐Debrinski, 2013, Biochimica et biophysica acta.

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.

D. Wallace, M. Lott, J. Shoffner, 1992, Mutation research.

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.

M. Beal, D. Wallace, A. McKee, 1994, Genomics.

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

M. Beal, D. Wallace, M. Lott, 1992, Nature Genetics.

Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits.

P. Bénit, J. Sahel, P. Rustin, 2007, Rejuvenation research.

The role of the 3' untranslated region in mRNA sorting to the vicinity of mitochondria is conserved from yeast to human cells.

C. Jacq, A. Margeot, G. Dujardin, 2003, Molecular biology of the cell.

Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction.

J. Sahel, S. Picaud, V. Forster, 2008, American journal of human genetics.

Brain oxidative damage in murine models of neonatal hypoxia/ischemia and reoxygenation.

P. Gressens, I. Torres-Cuevas, M. Corral‐Debrinski, 2019, Free radical biology & medicine.

Neuroglobin involvement in respiratory chain function and retinal ganglion cell integrity.

J. Sahel, P. Rustin, M. Marden, 2012, Biochimica et biophysica acta.

Mitochondrial DNA mutations in human degenerative diseases and aging.

D. Wallace, M. Lott, S. Ballinger, 1995, Biochimica et biophysica acta.

Neuroglobin Can Prevent or Reverse Glaucomatous Progression in DBA/2J Mice

Christophe Lechauve, Hong Liang, F. Brignole-Baudouin, 2017, Molecular therapy. Methods & clinical development.

Transient mitochondrial transcript level decay in oxidative stressed chondrocytes

M. Adolphe, M. Corral‐Debrinski, F. Vincent, 1994, Journal of cellular physiology.

Neuroglobin gene therapy prevents optic atrophy and preserves durably visual function in Harlequin mice.

J. Sahel, Christophe Lechauve, T. Debeir, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.