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

Human molecular genetics, 2011-10, Vol.20 (2), p.R116-R123

2011

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Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues

Neurobiology of disease, 2012-01, Vol.45 (1), p.264-271

2012

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Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

Human molecular genetics, 2001-11, Vol.10 (23), p.2717-2726

2001

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Neuroglial miscommunication in the cerebellum of a mouse model of myotonic dystrophy

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S213-S213

2015

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O.6 Antisense approach for myotonic dystrophy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.681-681

2011

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Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability

Human molecular genetics, 2000-05, Vol.9 (8), p.1185-1194

2000

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Defective satellite cells in congenital myotonic dystrophy

Human molecular genetics, 2001-09, Vol.10 (19), p.2079-2087

2001

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FP.44 Exploring the role of MuscleBlind-Like proteins in the regulation of CaVB1 isoform expression in adult skeletal muscle

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S129

2022

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Compressed-air work is entering the field of high pressures

Undersea & hyperbaric medicine, 2010-07, Vol.37 (4), p.193

2010

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The expansion of 300 CTG repeats in myotonic dystrophy transgenic mice does not induce sensory or motor neuropathy

Acta neuropathologica, 2007-08, Vol.114 (2), p.175-185

2007

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Maternal germline-specific effect of DNA ligase I on CTG/CAG instability

Human molecular genetics, 2011-06, Vol.20 (11), p.2131-2143

2011

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O.32Genome editing of expanded CTG repeats within the human DMPK gene reduces nuclear RNA foci in muscle of DM1 mice

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S125-S125

2019

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T.O.4 Ribozyme-based gene therapy reverses muscle atrophy in a mouse model of myotonic dystrophy

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.899-899

2007

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G.P.14.09 Functional characterization of skeletal muscles in DM1 mice

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.856-857

2007

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Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice

Human genetics, 2006-06, Vol.119 (5), p.520-526

2006

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CTG repeat instability and size variation timing in DNA repair-deficient mice

The EMBO journal, 2003-05, Vol.22 (9), p.2264-2273

2003

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CRISPR/Cas9-mediated genome editing corrects splicing alterations in myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S181

2017

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P.278 - CRISPR/Cas9-mediated genome editing corrects splicing alterations in myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S181-S181

2017

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Apnées obstructives et mixtes chez le souriceau DMSXL, modèle de la forme congénitale de la maladie de Steinert

Revue des maladies respiratoires, 2021-06, Vol.38 (6), p.593-594

2021

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Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

Molecular and Cellular Biology, 1991-09, Vol.11 (9), p.4679-4689

1991

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Spiritual Kinship in Europe, 1500-1900

1, 2012

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Longitudinal in vivo muscle function analysis of the DMSXL mouse model of myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2013-12, Vol.23 (12), p.1016-1025

2013

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MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice

Molecular and Cellular Biology, 2004-01, Vol.24 (2), p.629-637

2004

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Myotonic Dystrophy Transgenic Mice Exhibit Pathologic Abnormalities in Diaphragm Neuromuscular Junctions and Phrenic Nerves

Journal of neuropathology and experimental neurology, 2008-08, Vol.67 (8), p.763-772

2008

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La mortalité par cancer en France métropolitaine. Tendances récentes (2000–2003)

Oncologie (Paris, France), 2006-12, Vol.8 (10), p.911-926

2006

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

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

Neuroglial miscommunication in the cerebellum of a mouse model of myotonic dystrophy

O.6 Antisense approach for myotonic dystrophy

Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability

Defective satellite cells in congenital myotonic dystrophy

FP.44 Exploring the role of MuscleBlind-Like proteins in the regulation of CaVB1 isoform expression in adult skeletal muscle

Compressed-air work is entering the field of high pressures

The expansion of 300 CTG repeats in myotonic dystrophy transgenic mice does not induce sensory or motor neuropathy

Maternal germline-specific effect of DNA ligase I on CTG/CAG instability

O.32Genome editing of expanded CTG repeats within the human DMPK gene reduces nuclear RNA foci in muscle of DM1 mice

T.O.4 Ribozyme-based gene therapy reverses muscle atrophy in a mouse model of myotonic dystrophy

G.P.14.09 Functional characterization of skeletal muscles in DM1 mice

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice

CTG repeat instability and size variation timing in DNA repair-deficient mice

CRISPR/Cas9-mediated genome editing corrects splicing alterations in myotonic dystrophy type 1

P.278 - CRISPR/Cas9-mediated genome editing corrects splicing alterations in myotonic dystrophy type 1

Apnées obstructives et mixtes chez le souriceau DMSXL, modèle de la forme congénitale de la maladie de Steinert

Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

Spiritual Kinship in Europe, 1500-1900

Longitudinal in vivo muscle function analysis of the DMSXL mouse model of myotonic dystrophy type 1

MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice

Myotonic Dystrophy Transgenic Mice Exhibit Pathologic Abnormalities in Diaphragm Neuromuscular Junctions and Phrenic Nerves

La mortalité par cancer en France métropolitaine. Tendances récentes (2000–2003)

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