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List of works by Capucine Trollet

A negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis

scientific article published on 22 March 2022

Adeno-associated virus-8-mediated intravenous transfer of myostatin propeptide leads to systemic functional improvements of slow but not fast muscle

scientific article published in April 2009

Anti-prion Drugs Targeting the Protein Folding Activity of the Ribosome Reduce PABPN1 Aggregation

scientific article published on 02 February 2021

Atrophy, Fibrosis, and Increased PAX7-Positive Cells in Pharyngeal Muscles of Oculopharyngeal Muscular Dystrophy Patients

article published in 2013

Autologous myoblast transplantation for oculopharyngeal muscular dystrophy: a phase I/IIa clinical study

scientific article

Cellular Therapies for Muscular Dystrophies: Frustrations and Clinical Successes

scientific article published on 10 December 2015

Central Role of Transforming Ggrowth Factor Type Beta 1 in Skeletal Muscle Dysfunctions: an Update on Therapeutic strategies.

scientific article published on 16 November 2017

Codon and mRNA Sequence Optimization of Microdystrophin Transgenes Improves Expression and Physiological Outcome in Dystrophic mdx Mice Following AAV2/8 Gene Transfer

article

Combination of myostatin pathway interference and dystrophin rescue enhances tetanic and specific force in dystrophic mdx mice

scientific article

Combined methods to evaluate human cells in muscle xenografts

scientific article published on 02 May 2019

Correlation between PABPN1 genotype and disease severity in oculopharyngeal muscular dystrophy.

scientific article published on 23 December 2016

Current advances in cell therapy strategies for muscular dystrophies

scientific article published on February 2011

DNA electroporation in rabbits as a method for generation of high-titer neutralizing antisera: examples of the botulinum toxins types A, B, and E

scientific article published on 22 July 2013

Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx mice.

scientific article published on 25 May 2011

Delivery of DNA into muscle for treating systemic diseases: advantages and challenges

scientific article published on January 2008

Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients

scientific article published on 4 April 2011

Design of phosphorodiamidate morpholino oligomers (PMOs) for the induction of exon skipping of the human DMD gene.

scientific article

Electrotransfer into skeletal muscle for protein expression

scientific article published on October 2006

Established PABPN1 intranuclear inclusions in OPMD muscle can be efficiently reversed by AAV-mediated knockdown and replacement of mutant expanded PABPN1

scientific article published on 01 October 2019

Gene therapy for muscular dystrophy: current progress and future prospects.

scientific article published on July 2009

Generation of high-titer neutralizing antibodies against botulinum toxins A, B, and E by DNA electrotransfer.

scientific article published on 23 February 2009

Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders

scientific article

Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD)

scientific article published on 07 May 2019

Invited review: Stem cells and muscle diseases: advances in cell therapy strategies

scientific article

Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis

scientific article

Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres

scientific article

Nuclear entrapment and extracellular depletion of PCOLCE is associated with muscle degeneration in oculopharyngeal muscular dystrophy

scientific article

Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing

scientific article published on 09 August 2016

Optical imaging of luminescence for in vivo quantification of gene electrotransfer in mouse muscle and knee.

scientific article

Oxidative Stress in Disease and Aging: Mechanisms and Therapies 2016.

scientific article published on 26 January 2017

PABPN1 gene therapy for oculopharyngeal muscular dystrophy

scientific article published on 31 March 2017

Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophy

scientific article published on 01 May 2019

Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation

scientific article

Positive in vivo heterologous gene regulation by electric pulses delivery with metallothionein I gene promoter

scientific article published in December 2005

Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway

scientific article published on 25 March 2010

RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology

scientific article

Role of Oxidized Protein Repair in Human Skeletal Muscle.

scientific article published in October 2014

The Rag2⁻Il2rb⁻Dmd⁻ mouse: a novel dystrophic and immunodeficient model to assess innovating therapeutic strategies for muscular dystrophies

scientific article published on 23 August 2013

Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractile apparatus organization

scientific article

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