S. Duguez

发表

Muscle Gene Sets: a versatile methodological aid to functional genomics in the neuromuscular field

A. Malatras, S. Duguez, W. Duddy, 2019, Skeletal Muscle.

The Neurotoxicity of Vesicles Secreted by ALS Patient Myotubes Is Specific to Exosome-Like and Not Larger Subtypes

P. Pradat, S. Duguez, W. Duddy, 2022, Cells.

Mitochondrial biogenesis during skeletal muscle regeneration.

C. Denis, D. Freyssenet, L. Féasson, 2002, American journal of physiology. Endocrinology and metabolism.

MyoMiner: explore gene co-expression in normal and pathological muscle

I. Michalopoulos, G. Butler-Browne, A. Malatras, 2020, BMC Medical Genomics.

Personalized Medicine and Molecular Interaction Networks in Amyotrophic Lateral Sclerosis (ALS): Current Knowledge

S. Duguez, W. Duddy, Stephen Morgan, 2018, Journal of personalized medicine.

Age-Associated Methylation Suppresses SPRY1, Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle.

A. Bigot, G. Butler-Browne, V. Mouly, 2015, Cell reports.

Optimized method for extraction of exosomes from human primary muscle cells

S. Duguez, W. Duddy, E. Anakor, 2020, Skeletal Muscle.

Age-dependent alteration in muscle regeneration: the critical role of tissue niche

A. Musarò, C. Franceschi, M. Narici, 2013, Biogerontology.

The isolated muscle fibre as a model of disuse atrophy: characterization using PhAct, a method to quantify f-actin.

T. Partridge, S. Duguez, W. Duddy, 2011, Experimental cell research.

Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics.

K. Fischbeck, Barrington G. Burnett, L. Chernomordik, 2014, Human molecular genetics.

GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome

R. Finkel, K. Bushby, J. Jaiswal, 2020, Annals of neurology.

Regulation of ubiquitin–proteasome system, caspase enzyme activities, and extracellular proteinases in rat soleus muscle in response to unloading

C. Denis, D. Freyssenet, L. Féasson, 2007, Pflügers Archiv - European Journal of Physiology.

Bodywide skipping of exons 45–55 in dystrophic mdx52 mice by systemic antisense delivery

E. Hoffman, A. Nakamura, S. Takeda, 2012, Proceedings of the National Academy of Sciences.

Δ-9,11 Modification of Glucocorticoids Dissociates Nuclear Factor-κB Inhibitory Efficacy from Glucocorticoid Response Element-Associated Side Effects

E. Hoffman, D. DuBois, J. Mccall, 2012, Journal of Pharmacology and Experimental Therapeutics.

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

V. Meininger, F. Salachas, D. Devos, 2022, Journal of cachexia, sarcopenia and muscle.

Muscle cells of sporadic ALS patients secrete neurotoxic vesicles

V. Meininger, F. Salachas, D. Devos, 2021, medRxiv.

The Role of Sphingomyelin and Ceramide in Motor Neuron Diseases

K. Morrison, J. Mcconville, S. Duguez, 2022, Journal of personalized medicine.

Δ-9 , 11 modification of glucocorticoids dissociate NF-κ B inhibitory efficacy from GRE-associated side effects

Nagaraju, E. Hoffman, D. DuBois, 2012 .

Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia

K. Nagaraju, T. Partridge, V. Gnocchi, 2015, Skeletal Muscle.

The Rag2-Il2rb-Dmd- Mouse: a Novel Dystrophic and Immunodeficient Model to Assess Innovating Therapeutic Strategies for Muscular Dystrophies.

E. Füchtbauer, G. Butler-Browne, V. Mouly, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

The Rag 2 – Il 2 rb – Dmd – Mouse : a Novel Dystrophic and Immunodeficient Model to Assess Innovating Therapeutic Strategies for Muscular Dystrophies

E. Füchtbauer, G. Butler-Browne, V. Mouly, 2022 .

Necrotizing Soft Tissue Infections S.aureus - but not S.pyogenes- isolates display high rate of internalization and cytotoxicity toward human myoblasts.

V. M. D. Martins dos Santos, F. Vandenesch, P. Leblanc, 2019, The Journal of infectious diseases.

Necrotizing Soft Tissue Infections Staphylococcus aureus - but not Streptococcus pyogenes-isolates display high rate of internalization and cytotoxicity toward human myoblasts

F. Vandenesch, P. Leblanc, A. Norrby-Teglund, 2019, bioRxiv.

The Cellular and Molecular Signature of ALS in Muscle

S. Duguez, W. Duddy, E. Anakor, 2022, Journal of personalized medicine.

Genome-Wide Gene-Set Analysis Approaches in Amyotrophic Lateral Sclerosis

S. Duguez, W. Duddy, C. Vasilopoulou, 2022, Journal of personalized medicine.

HGCA2.0: An RNA-Seq Based Webtool for Gene Coexpression Analysis in Homo sapiens

I. Michalopoulos, V. Iconomidou, A. Malatras, 2023, Cells.

Extracellular Vesicles in Amyotrophic Lateral Sclerosis

K. Morrison, S. Duguez, W. Duddy, 2022, Life.

Exosomes in Ageing and Motor Neurone Disease: Biogenesis, Uptake Mechanisms, Modifications in Disease and Uses in the Development of Biomarkers and Therapeutics

S. Duguez, W. Duddy, J. Dumonceaux, 2021, Cells.

Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System

K. Mamchaoui, V. Mouly, F. Bernardi, 2017, Neuromuscular Disorders.

Molecular and Cellular Mechanisms Affected in ALS

S. Duguez, W. Duddy, E. Anakor, 2020, Journal of personalized medicine.

Gene therapy with AR isoform 2 rescues spinal and bulbar muscular atrophy phenotype by modulating AR transcriptional activity

K. Fischbeck, Jesse Dabney, A. Khvorova, 2021, Science Advances.

Calpain 3: a key regulator of the sarcomere?

Isabelle Richard, Marc Bartoli, I. Richard, 2006, The FEBS journal.

Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS

S. Duguez, W. Duddy, G. McCluskey, 2023, International journal of molecular sciences.

What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis?

George Giannakopoulos, Christina Vasilopoulou, Andrew P Morris, 2020, Journal of personalized medicine.

Myogenic and nonmyogenic cells differentially express proteinases, Hsc/Hsp70, and BAG-1 during skeletal muscle regeneration.

D. Freyssenet, L. Féasson, S. Duguez, 2003, American journal of physiology. Endocrinology and metabolism.

Molecular adaptations of neuromuscular disease‐associated proteins in response to eccentric exercise in human skeletal muscle

C. Denis, I. Richard, D. Freyssenet, 2002, The Journal of physiology.

A Systematic Review of Genotype–Phenotype Correlation across Cohorts Having Causal Mutations of Different Genes in ALS

S. Duguez, W. Duddy, C. Donaghy, 2020, Journal of personalized medicine.

Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy

F. Puppo, F. Magdinier, G. Butler-Browne, 2015, Annals of neurology.

A new pathway encompassing calpain 3 and its newly identified substrate cardiac ankyrin repeat protein is involved in the regulation of the nuclear factor‐κB pathway in skeletal muscle

Isabelle Richard, Marc Bartoli, N. Bourg, 2010, The FEBS journal.

Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

A. Bigot, K. Mamchaoui, V. Mouly, 2016, Skeletal Muscle.

A Systematic Review of Suggested Molecular Strata, Biomarkers and Their Tissue Sources in ALS

A. Bjourson, S. Duguez, W. Duddy, 2019, Front. Neurol..

Optimized Molecular Interaction Networks for the Study of Skeletal Muscle.

A. Malatras, S. Duguez, W. Duddy, 2021, Journal of neuromuscular diseases.

Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion

Y. Hathout, A. Bigot, G. Butler-Browne, 2013, Cellular and Molecular Life Sciences.

Age-Associated Methylati on Suppresses SPRY 1 , Leading to a Failure of Re-quiescence and Loss of the Reserve Stem Cell Pool in Elderly Muscle Graphical

A. Bigot, G. Butler-Browne, V. Mouly, 2022 .

Changes in Communication between Muscle Stem Cells and their Environment with Aging

V. Mouly, M. Thorley, A. Malatras, 2015, Journal of neuromuscular diseases.

G.O.15 Correlation between low FAT1 expression and early affected muscle in FSHD

F. Puppo, F. Magdinier, G. Butler-Browne, 2015, Neuromuscular Disorders.

Epidemiology and survival trends of motor neurone disease in Northern Ireland from 2015 to 2019

K. Morrison, S. Duguez, W. Duddy, 2021, European journal of neurology.

Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function

S. Duguez, W. Duddy, 2021, Journal of personalized medicine.

CellWhere: graphical display of interaction networks organized on subcellular localizations

Apostolos Malatras, William Duddy, Matthew Thorley, 2015, Nucleic Acids Res..

Expression and modification proteomics during skeletal muscle ageing

B. Friguet, G. Butler-Browne, D. Béchet, 2013, Biogerontology.

Advances in the proteomic investigation of the cell secretome

Y. Hathout, B. Rood, J. Nazarian, 2012, Expert review of proteomics.

Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

A. Bigot, K. Mamchaoui, V. Mouly, 2016, Skeletal Muscle.

Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion

Y. Hathout, A. Bigot, G. Butler-Browne, 2013, Cellular and Molecular Life Sciences.

Serum Neurofilaments in Motor Neuron Disease and Their Utility in Differentiating ALS, PMA and PLS

K. Morrison, J. Mcconville, S. Duguez, 2023, Life.

Mitochondrial-dependent regulation of myoblast proliferation.

D. Freyssenet, S. Duguez, O. Sabido, 2004, Experimental cell research.

Muscle Gene Sets: a versatile methodological aid to functional genomics in the neuromuscular field

A. Malatras, S. Duguez, W. Duddy, 2019, Skeletal Muscle.

MyoMiner: explore gene co-expression in normal and pathological muscle

I. Michalopoulos, G. Butler-Browne, A. Malatras, 2020, BMC Medical Genomics.

Expression and modification proteomics during skeletal muscle ageing

B. Friguet, G. Butler-Browne, D. Béchet, 2013, Biogerontology.

Atmospheric Oxygen Tension Slows Myoblast Proliferation via Mitochondrial Activation

T. Partridge, V. Gnocchi, S. Duguez, 2012, PloS one.

Skeletal muscle sings a choral stem cell lullaby.

T. Partridge, S. Duguez, 2009, Cell stem cell.