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Structural analysis of the NK-lysin-derived peptide NK-2 upon interaction with bacterial membrane mimetics consisting of phosphatidylethanolamine and phosphatidylglycerol

Biochimica et biophysica acta. Biomembranes, 2024-03, Vol.1866 (3), p.184267-184267, Article 184267

2024

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Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model

Scientific reports, 2019-02, Vol.9 (1), p.1580-1580, Article 1580

2019

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Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy

EMBO molecular medicine, 2018-02, Vol.10 (2), p.239-253

2018

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Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations

Molecular therapy. Nucleic acids, 2022-09, Vol.29, p.733-748

2022

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A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

Human molecular genetics, 2010-12, Vol.19 (24), p.4820-4836

2010

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Contemporary dual-mobility cup regional and private register: methodology and results

International orthopaedics, 2017-03, Vol.41 (3), p.439-445

2017

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Dynamin 2 and human diseases

Journal of molecular medicine (Berlin, Germany), 2010-04, Vol.88 (4), p.339-350

2010

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Therapy for dominant inherited diseases by allele-specific RNA interference: successes and pitfalls

Current gene therapy, 2015-01, Vol.15 (5), p.503-510

2015

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Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy

Molecular therapy. Nucleic acids, 2022-03, Vol.27, p.1179-1190

2022

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Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy

Molecular therapy. Nucleic acids, 2018-03, Vol.10, p.376-386

2018

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A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice

Traffic (Copenhagen, Denmark), 2012-06, Vol.13 (6), p.869-879

2012

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Skeletal Muscle Biopsy Analysis in Reducing Body Myopathy and Other FHL1-Related Disorders

Journal of neuropathology and experimental neurology, 2013-09, Vol.72 (9), p.833-845

2013

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Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing

Molecular therapy. Nucleic acids, 2016-09, Vol.5 (9), p.e362-e362, Article e362

2016

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What Are the Causes for Failures of Primary Hip Arthroplasties in France?

Clinical orthopaedics and related research, 2013-12, Vol.471 (12), p.3863-3869

2013

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A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation

Neurology, 2009-01, Vol.72 (1), p.93-95

2009

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Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

Cardiovascular research, 2004-08, Vol.63 (2), p.293-304

2004

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Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

Annals of neurology, 2007-12, Vol.62 (6), p.666-670

2007

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Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis

Human mutation, 2009-10, Vol.30 (10), p.1419-1427

2009

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Allele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy

Circulation. Arrhythmia and electrophysiology, 2017-12, Vol.10 (12), p.428-431

2017

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Trans trochanteric approach with coronal osteotomy of the great trochanter: A new technique for extra-capsular trochanteric fracture patients treated by total hip arthroplasty (THA) in elderly

SICOT-J, 2015-06, Vol.1, p.7-7

2015

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Intravenous Thrombolysis before Complete Angiographic Reperfusion: Beyond Angiographic Assessment to Target Microvascular Obstruction?

Annals of neurology, 2024-04, Vol.95 (4), p.762-773

2024

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Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy

EMBO molecular medicine, 2017-12, Vol.10, p.239-253

2017

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A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: Clinical and pathological findings

Neuromuscular disorders : NMD, 2008-04, Vol.18 (4), p.334-338

2008

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Trans trochanteric approach with coronal osteotomy of the great trochanter

SICOT-J, 2015-01, Vol.1, p.7

2015

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Rescue intracranial permanent stenting for refractory occlusion following thrombectomy: a propensity matched analysis

Journal of neurointerventional surgery, 2024-02, Vol.16 (2), p.115-123

2024

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Structural analysis of the NK-lysin-derived peptide NK-2 upon interaction with bacterial membrane mimetics consisting of phosphatidylethanolamine and phosphatidylglycerol

Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model

Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy

Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

Contemporary dual-mobility cup regional and private register: methodology and results

Dynamin 2 and human diseases

Therapy for dominant inherited diseases by allele-specific RNA interference: successes and pitfalls

Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy

Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy

A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice

Skeletal Muscle Biopsy Analysis in Reducing Body Myopathy and Other FHL1-Related Disorders

Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing

What Are the Causes for Failures of Primary Hip Arthroplasties in France?

A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis

Allele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy

Trans trochanteric approach with coronal osteotomy of the great trochanter: A new technique for extra-capsular trochanteric fracture patients treated by total hip arthroplasty (THA) in elderly

Intravenous Thrombolysis before Complete Angiographic Reperfusion: Beyond Angiographic Assessment to Target Microvascular Obstruction?

Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy

A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: Clinical and pathological findings

Trans trochanteric approach with coronal osteotomy of the great trochanter

Rescue intracranial permanent stenting for refractory occlusion following thrombectomy: a propensity matched analysis

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