M. Gomes-Pereira

发表

Non-ATG–initiated translation directed by microsatellite expansions

Brian B. Gibbens, M. Swanson, W. Low, 2010, Proceedings of the National Academy of Sciences.

Ethidium Bromide Modifies The Agarose Electrophoretic Mobility of CAG•CTG Alternative DNA Structures Generated by PCR

D. Monckton, M. Gomes-Pereira, 2017, Front. Cell. Neurosci..

Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy

G. Cheron, M. Swanson, A. Leroy, 2017, Cell reports.

Disease neuropathogenesis beyond missplicing

L. Buée, N. Sergeant, O. Hernández-Hernández, 2013 .

Synaptic protein dysregulation in myotonic dystrophy type 1

A. Munnich, L. Buée, N. Sergeant, 2013, Rare diseases.

Myotonic dystrophy mouse models: towards rational therapy development.

T. Cooper, M. Gomes-Pereira, G. Gourdon, 2011, Trends in molecular medicine.

Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue specificity, but no association with cell division rates.

D. Monckton, M. Gomes-Pereira, D G Monckton, 2001, Human molecular genetics.

Disease-associated CAG·CTG triplet repeats expand rapidly in non-dividing mouse cells, but cell cycle arrest is insufficient to drive expansion

D. Monckton, J. Hilley, M. Gomes-Pereira, 2014, Nucleic acids research.

Chronic Exposure to Cadmium and Antioxidants Does Not Affect the Dynamics of Expanded CAG•CTG Trinucleotide Repeats in a Mouse Cell Culture System of Unstable DNA

D. Monckton, M. Gomes-Pereira, 2021, Frontiers in Cellular Neuroscience.

CTG Trinucleotide Repeat “Big Jumps”: Large Expansions, Small Mice

A. Munnich, C. Junien, M. Gomes-Pereira, 2007, PLoS genetics.

Myotonic dystrophy RNA toxicity alters morphology, adhesion and migration of mouse and human astrocytes

N. Rouach, D. Auboeuf, A. González-Barriga, 2021, Nature Communications.

Defects in Mouse Cortical Glutamate Uptake Can Be Unveiled In Vivo by a Two-in-One Quantitative Microdialysis.

S. Parrot, J. Comte, M. Gomes-Pereira, 2021, ACS chemical neuroscience.

Chemically induced increases and decreases in the rate of expansion of a CAG*CTG triplet repeat.

D. Monckton, M. Gomes-Pereira, 2004, Nucleic acids research.

Of Mice and Men: Advances in the Understanding of Neuromuscular Aspects of Myotonic Dystrophy

M. Gomes-Pereira, G. Gourdon, Sandra O. Braz, 2018, Front. Neurol..

Muscleblind-like 2-Mediated Alternative Splicing in the Developing Brain and Dysregulation in Myotonic Dystrophy

M. Ares, R. Darnell, M. Cline, 2012, Neuron.

RNA toxicity in human disease and animal models: from the uncovering of a new mechanism to the development of promising therapies.

G. Sicot, M. Gomes-Pereira, 2013, Biochimica et biophysica acta.

Chemical modifiers of unstable expanded simple sequence repeats: what goes up, could come down.

D. Monckton, M. Gomes-Pereira, 2006, Mutation research.

MBNL‐dependent impaired development within the neuromuscular system in myotonic dystrophy type 1

C. Legay, D. Furling, A. González-Barriga, 2022, Neuropathology and applied neurobiology.

Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.

L. Ingram, D. Monckton, M. Gomes-Pereira, 2004, Human molecular genetics.

DM1 Transgenic Mice Exhibit Abnormal Neurotransmitter Homeostasis and Synaptic Plasticity in Association with RNA Foci and Mis-Splicing in the Hippocampus

P. Dutar, S. Parrot, B. Potier, 2022, International journal of molecular sciences.

Analysis of unstable triplet repeats using small-pool polymerase chain reaction.

S. Bidichandani, D. Monckton, M. Gomes-Pereira, 2004, Methods in molecular biology.

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.

F. Metzger, A. Munnich, L. Buée, 2013, Brain : a journal of neurology.

Molecular, Physiological, and Motor Performance Defects in DMSXL Mice Carrying >1,000 CTG Repeats from the Human DM1 Locus

F. Metzger, A. Munnich, A. Hoeflich, 2012, PLoS genetics.

Myotonic dystrophy, when simple repeats reveal complex pathogenic entities: new findings and future challenges.

G. Sicot, M. Gomes-Pereira, G. Gourdon, 2011, Human molecular genetics.

Integrative Cell Type-Specific Multi-Omics Approaches Reveal Impaired Programs of Glial Cell Differentiation in Mouse Culture Models of DM1

J. Claude, D. Auboeuf, I. Guerrera, 2021, Frontiers in Cellular Neuroscience.

Chapter 36 - Transgenic Mouse Models of Unstable Trinucleotide Repeats: Toward an Understanding of Disease-Associated Repoeat Size Mutation

M. Gomes-Pereira, G. Gourdon, Laurent Foiry, 2006 .

DM1 CTG expansions affect insulin receptor isoforms expression in various tissues of transgenic mice.

C. Junien, G. Bassez, M. Gomes-Pereira, 2007, Biochimica et biophysica acta.

Non-Radioactive Detection of Trinucleotide Repeat Size Variability

M. Gomes-Pereira, G. Gourdon, S. Tomé, 2014, PLoS currents.

Non-Radioactive Detection of Trinucleotide Repeat Size

M. Gomes-Pereira, G. Gourdon, S. Tomé, 2014 .

Mouse tissue culture models of unstable triplet repeats.

D. Monckton, M. Gomes-Pereira, 2004, Methods in molecular biology.

Myotonic dystrophy type 1-associated CTG repeats disturb the expression and subcellular distribution of microtubule-associated proteins MAP1A, MAP2, and MAP6/STOP in PC12 cells

O. Hernández-Hernández, B. Cisneros, F. García-Sierra, 2011, Molecular Biology Reports.

Consensus on cerebral involvement in myotonic dystrophy Workshop report: May 24–27, 2013, Ferrere (AT), Italy

G. Meola, G. Bassez, L. Ranum, 2014, Neuromuscular Disorders.

Upregulation of FasII underlies synergistic neuropathological and behavioral defects in a Drosophila model of myotonic dystrophy

Z. Chen, A. Koon, A. Bargiela, 2024, bioRxiv.

Defects in Mouse Cortical Glutamate Uptake Can Be Unveiled In Vivo by a Two-in-One Quantitative Microdialysis.

J. Comte, M. Gomes-Pereira, Aline Huguet-Lachon, 2021, ACS chemical neuroscience.