Publications by authors named "Nicolas Lévy"

100Publications

Evidence of SARS-CoV-2 re-infection with a different genotype.

J Infect 2020 Nov 15. Epub 2020 Nov 15.

IHU Méditerranée Infection, 19-21 boulevard Jean Moulin, 13005 Marseille, France; Aix-Marseille Univ., Institut de Recherche pour le Développement (IRD), Microbes Evolution Phylogeny and Infections (MEPHI), Assistance Publique - Hôpitaux de Marseille (AP-HM), 19-21 boulevard Jean Moulin, 13005 Marseille, France. Electronic address:

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http://dx.doi.org/10.1016/j.jinf.2020.11.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666873PMC
November 2020

Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy.

Ann Clin Transl Neurol 2020 Oct 27. Epub 2020 Oct 27.

Centre de Référence des Maladies Neuromusculaires PACA-Réunion-Rhônes-Alpes, CHU La Réunion, France.

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http://dx.doi.org/10.1002/acn3.51193DOI Listing
October 2020

Refining NGS diagnosis of muscular disorders.

J Neurol Neurosurg Psychiatry 2020 Sep 15. Epub 2020 Sep 15.

Aix-Marseille Université, Inserm, U1251-MMG, Marseille Medical Genetics, Marseille, France.

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http://dx.doi.org/10.1136/jnnp-2018-319254DOI Listing
September 2020

Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assay.

Hum Mutat 2020 Jul 15. Epub 2020 Jul 15.

Faculté des Sciences Médicales et Paramédicales, Marseille Medical Genetics, Aix Marseille Université, INSERM, Marseille, France.

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http://dx.doi.org/10.1002/humu.24083DOI Listing
July 2020

[CRISPR-Cas9 for muscle dystrophies].

Med Sci (Paris) 2020 Apr 1;36(4):358-366. Epub 2020 May 1.

Aix Marseille Univ, Inserm, MMG, U1251, 13005 Marseille, France - AP-HM Département de Génétique Médicale, Hôpital d'Enfants de la Timone, Marseille, 13005 France - GIPTIS, Genetics Institute for Patients Therapies Innovation and Science, 13002 Marseille, France.

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http://dx.doi.org/10.1051/medsci/2020081DOI Listing
April 2020

Hutchinson-Gilford progeria syndrome: Rejuvenating old drugs to fight accelerated ageing.

Methods 2020 Apr 9. Epub 2020 Apr 9.

CECS, I-STEM AFM, Institute for Stem Cell Therapy and Exploration of Monogenic Diseases, 28 rue Henri Desbruères, 91100 Corbeil-Essonnes, France. Electronic address:

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http://dx.doi.org/10.1016/j.ymeth.2020.04.005DOI Listing
April 2020

miR-9 Does Not Regulate Lamin A Expression in Metastatic Cells from Lung Adenocarcinoma.

Int J Mol Sci 2020 Feb 26;21(5). Epub 2020 Feb 26.

Aix Marseille Univ, APHM, INSERM, MMG, Hôpital la Timone, Service de Biologie Cellulaire, 13005 Marseille, France.

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http://dx.doi.org/10.3390/ijms21051599DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084260PMC
February 2020

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young.

Herz 2020 Jan 22. Epub 2020 Jan 22.

Biomedical Genomics and Oncogenetics Laboratory LR16IPT05, Institut Pasteur de Tunis, Université Tunis El Manar, 13 Place Pasteur, BP74-1002, Tunis, belvédère, Tunisia.

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http://dx.doi.org/10.1007/s00059-019-04883-1DOI Listing
January 2020

High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome.

Atherosclerosis 2020 01 12;293:86-91. Epub 2019 Dec 12.

MARS Cardio, Mediterranean Association for Research and Studies in Cardiology, Intensive Care Unit, Hospital Nord, Marseille, France; Aix Marseille Univ, INSERM, INRA, C2VN, Marseille, France. Electronic address:

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http://dx.doi.org/10.1016/j.atherosclerosis.2019.12.002DOI Listing
January 2020

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.

Authors:
Karim Wahbi Rabah Ben Yaou Estelle Gandjbakhch Frédéric Anselme Thomas Gossios Neal K Lakdawala Caroline Stalens Frédéric Sacher Dominique Babuty Jean-Noel Trochu Ghassan Moubarak Kostantinos Savvatis Raphaël Porcher Pascal Laforêt Abdallah Fayssoil Eloi Marijon Tanya Stojkovic Anthony Béhin Sarah Leonard-Louis Guilhem Sole Fabien Labombarda Pascale Richard Corinne Metay Susana Quijano-Roy Ivana Dabaj Didier Klug Marie-Christine Vantyghem Philippe Chevalier Pierre Ambrosi Emmanuelle Salort Nicolas Sadoul Xavier Waintraub Khadija Chikhaoui Philippe Mabo Nicolas Combes Philippe Maury Jean-Marc Sellal Usha B Tedrow Jonathan M Kalman Jitendra Vohra Alexander F A Androulakis Katja Zeppenfeld Tina Thompson Christine Barnerias Henri-Marc Bécane Eric Bieth Franck Boccara Damien Bonnet Françoise Bouhour Stéphane Boulé Anne-Claire Brehin Françoise Chapon Pascal Cintas Jean-Marie Cuisset Jean-Marc Davy Annachiara De Sandre-Giovannoli Florence Demurger Isabelle Desguerre Klaus Dieterich Julien Durigneux Andoni Echaniz-Laguna Romain Eschalier Ana Ferreiro Xavier Ferrer Christine Francannet Mélanie Fradin Bénédicte Gaborit Arnaud Gay Albert Hagège Arnaud Isapof Isabelle Jeru Raul Juntas Morales Emmanuelle Lagrue Nicolas Lamblin Olivier Lascols Vincent Laugel Arnaud Lazarus France Leturcq Nicolas Levy Armelle Magot Véronique Manel Raphaël Martins Michèle Mayer Sandra Mercier Christophe Meune Maud Michaud Marie-Christine Minot-Myhié Antoine Muchir Aleksandra Nadaj-Pakleza Yann Péréon Philippe Petiot Florence Petit Julien Praline Anne Rollin Pascal Sabouraud Catherine Sarret Stéphane Schaeffer Frederic Taithe Céline Tard Vincent Tiffreau Annick Toutain Camille Vatier Ulrike Walther-Louvier Bruno Eymard Philippe Charron Corinne Vigouroux Gisèle Bonne Saurabh Kumar Perry Elliott Denis Duboc

Circulation 2019 07 3;140(4):293-302. Epub 2019 Jun 3.

APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Centre de Référence de Pathologie Neuromusculaire Nord/Est/Ile de France, Paris-Descartes, Sorbonne Paris Cité University (K.W., D.D.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.118.039410DOI Listing
July 2019

Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy.

Circ Genom Precis Med 2019 05;12(5):e002500

Département de génétique médicale, APHM, Hôpital d'enfants de la Timone, Marseille, France. Aix Marseille University, INSERM, Marseille Medical Genetics, Faculté de Médecine, France (K.N., S.R., D.S., J.-P.D., M.C., F.M., C.B., N.L.).

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http://dx.doi.org/10.1161/CIRCGEN.119.002500DOI Listing
May 2019

Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants.

Hum Mutat 2019 06 28;40(6):661-674. Epub 2019 Mar 28.

Aix Marseille Univ, APHM, INSERM, MMG, Laboratory of Molecular Biology Hospital La Conception, Marseille, France.

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http://dx.doi.org/10.1002/humu.23746DOI Listing
June 2019

Dysferlin Exon 32 Skipping in Patient Cells.

Methods Mol Biol 2018 ;1828:489-496

Aix Marseille Univ, INSERM, Marseille Medical Genetics (MMG), Marseille, France.

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http://dx.doi.org/10.1007/978-1-4939-8651-4_31DOI Listing
April 2019

Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome.

Am J Med Genet A 2018 08 28;176(8):1760-1763. Epub 2018 Jul 28.

Peripheral Nervous System, Muscle and ALS Department, Nice University Hospital, Université Côte d'Azur, Nice, France.

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http://doi.wiley.com/10.1002/ajmg.a.38843
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http://dx.doi.org/10.1002/ajmg.a.38843DOI Listing
August 2018

Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features.

J Hum Genet 2018 Oct 25;63(10):1077-1082. Epub 2018 Jul 25.

Aix Marseille Univ, INSERM, Marseille Medical Genetics, U1251, Marseille, France.

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http://dx.doi.org/10.1038/s10038-018-0492-1DOI Listing
October 2018

Prediction of Mutations to Control Pathways Enabling Tumor Cell Invasion with the CoLoMoTo Interactive Notebook (Tutorial).

Front Physiol 2018 6;9:787. Epub 2018 Jul 6.

LRI UMR 8623, Centre National de la Recherche Scientifique, Université Paris-Sud, Université Paris-Saclay, Orsay, France.

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http://dx.doi.org/10.3389/fphys.2018.00787DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043725PMC
July 2018

Random walk with restart on multiplex and heterogeneous biological networks.

Bioinformatics 2019 02;35(3):497-505

Aix Marseille Univ, CNRS, Centrale Marseille, I2M, Marseille, France.

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http://dx.doi.org/10.1093/bioinformatics/bty637DOI Listing
February 2019

Lamins in Lung Cancer: Biomarkers and Key Factors for Disease Progression through miR-9 Regulation?

Cells 2018 Jul 16;7(7). Epub 2018 Jul 16.

Aix Marseille Université, APHM, INSERM, MMG, Hôpital la Timone, Service de Biologie Cellulaire, 13385 Marseille, France.

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http://dx.doi.org/10.3390/cells7070078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071028PMC
July 2018

The CoLoMoTo Interactive Notebook: Accessible and Reproducible Computational Analyses for Qualitative Biological Networks.

Front Physiol 2018 19;9:680. Epub 2018 Jun 19.

Laboratoire de Recherche en Informatique UMR8623, Université Paris-Sud, Centre National de la Recherche Scientifique, Université Paris-Saclay, Orsay, France.

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http://dx.doi.org/10.3389/fphys.2018.00680DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018415PMC
June 2018

Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospects.

Hum Mutat 2018 06 25;39(6):774-789. Epub 2018 Mar 25.

Molecular genetics Laboratory, Medical genetics and Cell biology Department, La Timone children's hospital, Assistance-Publique des Hôpitaux de Marseille (APHM), Marseille, France.

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http://dx.doi.org/10.1002/humu.23418DOI Listing
June 2018

Abnormal retention of nuclear lamina and disorganization of chromatin-related proteins in spermatozoa from DPY19L2-deleted globozoospermic patients.

Reprod Biomed Online 2017 Nov 4;35(5):562-570. Epub 2017 Aug 4.

Aix Marseille University, Inserm, GMGF, 13385 Marseille, Cedex 5, France; APHM Hôpital La Conception, Pôle Femmes-Parents-Enfants, Centre Clinico-Biologique d'Assistance Médicale à la Procréation-CECOS, 13385 Marseille, Cedex 5, France. Electronic address:

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http://dx.doi.org/10.1016/j.rbmo.2017.07.013DOI Listing
November 2017

Metformin decreases progerin expression and alleviates pathological defects of Hutchinson-Gilford progeria syndrome cells.

NPJ Aging Mech Dis 2016 10;2:16026. Epub 2016 Nov 10.

INSERM U861, I-STEM, AFM, Institute for Stem cell Therapy and Exploration of Monogenic Diseases, Corbeil Essonnes, France.

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http://dx.doi.org/10.1038/npjamd.2016.26DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515002PMC
November 2016

Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL).

Metabolism 2017 06 28;71:213-225. Epub 2017 Mar 28.

Aix Marseille Univ, INSERM, GMGF, Marseille, France; Department of Medical Genetics, Molecular genetics Laboratory, La Timone Children's Hospital, 264 Rue Saint Pierre, 13005, Marseille, France. Electronic address:

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http://dx.doi.org/10.1016/j.metabol.2017.03.011DOI Listing
June 2017

Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing.

Muscle Nerve 2017 Nov 7;56(5):993-997. Epub 2017 Apr 7.

Aix Marseille University, GMGF, INSERM AMU UMR_S910, Faculté de Médecine de Marseille, 4e étage Aile Verte, 27 Boulevard Jean Moulin, 13385, Marseille Cedex 05, France.

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http://dx.doi.org/10.1002/mus.25638DOI Listing
November 2017

Molecular combing: A new tool in diagnosing leukemia.

Cancer Biomark 2016 ;17(4):405-409

Département de Génétique Médicale, AP-HM La Timone, Marseille, France.

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http://dx.doi.org/10.3233/CBM-160656DOI Listing
March 2017

Novel mutations cause an aggressive atypical neonatal progeria without progerin accumulation.

J Med Genet 2016 Nov 22;53(11):776-785. Epub 2016 Jun 22.

Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología (IUOPA), Universidad de Oviedo, Oviedo, Spain.

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http://dx.doi.org/10.1136/jmedgenet-2015-103695DOI Listing
November 2016

Molecular density functional theory of water including density-polarization coupling.

J Phys Condens Matter 2016 06 26;28(24):244005. Epub 2016 Apr 26.

Max Planck Institute for Solid State Research, Heisenbergstraße 1, Stuttgart 70569, Germany.

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http://dx.doi.org/10.1088/0953-8984/28/24/244005DOI Listing
June 2016

Production of unstable proteins through the formation of stable core complexes.

Nat Commun 2016 Mar 17;7:10932. Epub 2016 Mar 17.

IGBMC, UDS, CNRS, INSERM, 1 rue Laurent Fries, 67404 Illkirch, France.

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http://dx.doi.org/10.1038/ncomms10932DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800440PMC
March 2016

A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene.

Int J Cardiol 2016 Apr 16;209:317-8. Epub 2016 Feb 16.

Department of Medical Genetics, La Timone Hospital, Aix Marseille Université, INSERM, GMGF UMR S 910, 13385 Marseille, France.

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http://dx.doi.org/10.1016/j.ijcard.2016.02.113DOI Listing
April 2016

Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutation.

Brain Dev 2016 May 10;38(5):498-506. Epub 2015 Dec 10.

Department of Neuropaediatrics, Timone Hospital, Marseille Teaching Hospital, France.

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http://dx.doi.org/10.1016/j.braindev.2015.11.006DOI Listing
May 2016

Dysferlinopathy in Iran: Clinical and genetic report.

J Neurol Sci 2015 Dec 11;359(1-2):256-9. Epub 2015 Nov 11.

Aix Marseille Université, INSERM, GMGF UMR_S 910, 13385 Marseille, France; Reference Center for Neuromuscular Disorders and ALS CHU La Timone Marseille, France.

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https://linkinghub.elsevier.com/retrieve/pii/S0022510X153001
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http://dx.doi.org/10.1016/j.jns.2015.11.009DOI Listing
December 2015

[First Italo-French meeting on laminopathies and other pathologies related to the nuclear envelope].

Med Sci (Paris) 2015 Nov 6;31 Spec No 3:39-40. Epub 2015 Nov 6.

Sorbonne Universités, UPMC Université Paris 06, Inserm UMRS974, CNRS FRE3617, Centre de Recherche en Myologie, Institut de Myologie, Paris, France.

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http://dx.doi.org/10.1051/medsci/201531s311DOI Listing
November 2015

Comment on: A novel dysferlin-mutant pseudoexon bypassed with antisense oligonucleotides.

Ann Clin Transl Neurol 2015 Jul;2(7):783-4

Aix Marseille Université, GMGF 13385, Marseille, France ; Inserm, UMR_S 910 13385, Marseille, France ; AP-HM, Département de Génétique Médicale et de Biologie Cellulaire, Hôpital d'Enfants de la Timone 13385, Marseille, France.

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http://dx.doi.org/10.1002/acn3.216DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531062PMC
July 2015

Respiratory and cardiac function in japanese patients with dysferlinopathy.

Muscle Nerve 2016 Mar 27;53(3):394-401. Epub 2016 Jan 27.

Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan.

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http://dx.doi.org/10.1002/mus.24741DOI Listing
March 2016

Toward an objective measure of functional disability in dysferlinopathy.

Muscle Nerve 2016 Jan 23;53(1):49-57. Epub 2015 May 23.

Unidad Neuromuscular, Departamento de Neurología y Neurocirugía, Hospital Clínico Universidad de Chile, Santos Dumont 999, 2do. piso, Sector E. Independencia, 8380456, Santiago, Chile.

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http://dx.doi.org/10.1002/mus.24685DOI Listing
January 2016

Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing.

J Neurol Neurosurg Psychiatry 2016 Mar 17;87(3):340-2. Epub 2015 Mar 17.

APHM, Department of Neurology, Neuromuscular and ALS Reference Center, La Timone University Hospital, Marseille, France Aix Marseille Université, INSERM, GMGF, Marseille, France.

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http://dx.doi.org/10.1136/jnnp-2014-309663DOI Listing
March 2016

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Eur J Hum Genet 2015 Aug 4;23(8):1051-61. Epub 2015 Feb 4.

1] Aix Marseille Université, INSERM, GMGF UMR_S 910, Marseille, France [2] Département de Génétique Médicale et de Biologie Cellulaire, AP-HM, Hôpital d'Enfants de la Timone, Marseille, France.

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http://dx.doi.org/10.1038/ejhg.2014.239DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795109PMC
August 2015

Vascular Endothelial Growth Factor A c.*237C>T polymorphism is associated with bevacizumab efficacy and related hypertension in metastatic colorectal cancer.

Dig Liver Dis 2015 Apr 30;47(4):331-7. Epub 2014 Dec 30.

Department of Digestive Oncology, Aix-Marseille University, Assistance Publique Hôpitaux de Marseille, Marseille, France; UMR S-910 INSERM, Medical Genetics and Functional Genomics, Aix-Marseille University, Marseille, France.

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http://dx.doi.org/10.1016/j.dld.2014.12.013DOI Listing
April 2015

Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy.

Neurol India 2014 Nov-Dec;62(6):635-9

Aix Marseille University, GMGF, 13385; Inserm, UMR_S 910, 13385; Department of Medical Genetics and Cell Biology, APHM, Children's Hospital La Timone, 13385, Marseille, France.

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http://search.proquest.com/openview/e70fd22cb0c480c42d20ceb3
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http://dx.doi.org/10.4103/0028-3886.149386DOI Listing
March 2015

Nuclear envelope remodelling during human spermiogenesis involves somatic B-type lamins and a spermatid-specific B3 lamin isoform.

Mol Hum Reprod 2015 Mar 4;21(3):225-36. Epub 2014 Dec 4.

Aix Marseille Université, INSERM, GMGF UMR_S 910, 13385, Marseille, France APHM Hôpital La Conception, Gynépôle, Laboratoire de Biologie de la Reproduction-CECOS, 13385 Marseille Cedex 5, France

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https://academic.oup.com/molehr/article-lookup/doi/10.1093/m
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http://dx.doi.org/10.1093/molehr/gau111DOI Listing
March 2015

Identification of splicing defects caused by mutations in the dysferlin gene.

Hum Mutat 2014 Dec;35(12):1532-41

Aix Marseille Université, GMGF, Marseille, 13385, France; Inserm, UMR_S 910, Marseille, 13385, France.

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http://dx.doi.org/10.1002/humu.22710DOI Listing
December 2014

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment.

Atherosclerosis 2014 Nov 28;237(1):45-52. Epub 2014 Aug 28.

APHM, CHU de la Timone, Laboratoire de Génétique Moléculaire, Marseille, France; Aix-Marseille Université, Inserm UMR_S U910, Faculté de Médecine, Marseille, France. Electronic address:

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http://dx.doi.org/10.1016/j.atherosclerosis.2014.08.036DOI Listing
November 2014

Exome sequencing as a second-tier diagnostic approach for clinically suspected dysferlinopathy patients.

Muscle Nerve 2014 Dec 30;50(6):1007-10. Epub 2014 Oct 30.

Aix Marseille Université, INSERM, GMGF, UMR_S 910, 13385, Marseille, France; APHM, Département de Génétique Médicale, Hôpital Timone Enfants, Marseille, 13385, France.

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http://dx.doi.org/10.1002/mus.24344DOI Listing
December 2014

Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers.

Neurology 2014 Aug 16;83(8):733-42. Epub 2014 Jul 16.

From Aix Marseille Universite (M.-C.G., S.R., C.D., A.T., G.B., E.S.-C., N.B., J.M., F.P., M.B., N.L., R.B., S.A., K.N., F.M.), INSERM GMGF UMR S_910, Marseille; and APHM, Centre de Référence des Maladies Neuromusculaires et de la SLA (E.S.-C., S.A.), and APHM, Laboratoire de Génétique Médicale (C.V., C.C., N.L., R.B., K.N.), Hôpital de la Timone, Marseille, France.

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http://dx.doi.org/10.1212/WNL.0000000000000708DOI Listing
August 2014

Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome.

BMC Med Genet 2014 May 2;15:51. Epub 2014 May 2.

Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología, Universidad de Oviedo, 33006 Oviedo, Spain.

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http://dx.doi.org/10.1186/1471-2350-15-51DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022398PMC
May 2014

Entire CAPN3 gene deletion in a patient with limb-girdle muscular dystrophy type 2A.

Muscle Nerve 2014 Sep 5;50(3):448-53. Epub 2014 Aug 5.

Neurosciences Area, Biodonostia Institute, Hospital Universitario Donostia, 20014, San Sebastián, Spain.

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http://dx.doi.org/10.1002/mus.24263DOI Listing
September 2014

A new lamin a mutation associated with acrogeria syndrome.

J Invest Dermatol 2014 Aug 1;134(8):2274-2277. Epub 2014 Apr 1.

Aix Marseille Université, GMGF, INSERM, UMR_S 910, Marseille, France. Electronic address:

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http://dx.doi.org/10.1038/jid.2014.158DOI Listing
August 2014

WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Semin Cell Dev Biol 2014 Mar 28. Epub 2014 Mar 28.

Aix-Marseille Université, UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France(1); INSERM, UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France(1); AP-HM, Département de Génétique Médicale, Hôpital d'enfants Timone, 264 Rue Saint Pierre, 13385 Marseille Cedex 5, France(3). Electronic address:

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http://dx.doi.org/10.1016/j.semcdb.2014.03.022DOI Listing
March 2014

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Semin Cell Dev Biol 2014 May 22;29:125-47. Epub 2014 Mar 22.

Aix-Marseille Université, UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France; INSERM, UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine, 27 Bd Jean Moulin, 13385 Marseille Cedex 5, France; AP-HM, Département de Génétique Médicale, Hôpital d'enfants Timone, 264 Rue Saint Pierre, 13385 Marseille Cedex 5, France. Electronic address:

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http://dx.doi.org/10.1016/j.semcdb.2014.03.021DOI Listing
May 2014