Literature DB >> 19944865

Interventions for muscular dystrophy: molecular medicines entering the clinic.

Kate Bushby1, Hanns Lochmüller, Stephen Lynn, Volker Straub.   

Abstract

Muscular dystrophies are individually rare genetic disorders that cause much chronic disability, affecting young children and adults. In the past 20 years, more than 30 genetic types of muscular dystrophy have been defined. During this time, precise diagnosis, genetic counselling, and medical management have improved. These advances in medical practice have occurred while definitive therapies based on an improved knowledge of disease pathogenesis are awaited. A wide range of therapeutic options have been tested in animal models, and some are being tested in clinical trials. Various therapeutic targets are being investigated, from personalised medicines targeting specific mutations and drugs targeting cellular pathways to gene-based and cell-based therapies.

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Year:  2009        PMID: 19944865     DOI: 10.1016/S0140-6736(09)61834-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  12 in total

1.  Proinflammatory signals and the loss of lymphatic vessel hyaluronan receptor-1 (LYVE-1) in the early pathogenesis of laminin alpha2-deficient skeletal muscle.

Authors:  Katherine E Wardrop; Janice A Dominov
Journal:  J Histochem Cytochem       Date:  2011-02       Impact factor: 2.479

Review 2.  Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin-angiotensin system.

Authors:  Rasna Sabharwal; Mark W Chapleau
Journal:  Exp Physiol       Date:  2013-12-13       Impact factor: 2.969

3.  Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapies.

Authors:  Nigel G Laing; Mark R Davis; Klair Bayley; Sue Fletcher; Steve D Wilton
Journal:  Clin Biochem Rev       Date:  2011-08

4.  Arrhythmogenic right ventricular cardiomyopathy. What is needed for a cure?

Authors:  G Thiene; I Rigato; K Pilichou; D Corrado; C Basso
Journal:  Herz       Date:  2012-09       Impact factor: 1.443

Review 5.  Pathophysiology of arrhythmogenic cardiomyopathy.

Authors:  Cristina Basso; Barbara Bauce; Domenico Corrado; Gaetano Thiene
Journal:  Nat Rev Cardiol       Date:  2011-11-29       Impact factor: 32.419

Review 6.  RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research.

Authors:  Rachel Thompson; Louise Johnston; Domenica Taruscio; Lucia Monaco; Christophe Béroud; Ivo G Gut; Mats G Hansson; Peter-Bram A 't Hoen; George P Patrinos; Hugh Dawkins; Monica Ensini; Kurt Zatloukal; David Koubi; Emma Heslop; Justin E Paschall; Manuel Posada; Peter N Robinson; Kate Bushby; Hanns Lochmüller
Journal:  J Gen Intern Med       Date:  2014-08       Impact factor: 5.128

7.  Improvement of cardiac contractile function by peptide-based inhibition of NF-κB in the utrophin/dystrophin-deficient murine model of muscular dystrophy.

Authors:  Dawn A Delfín; Ying Xu; Jennifer M Peterson; Denis C Guttridge; Jill A Rafael-Fortney; Paul Ml Janssen
Journal:  J Transl Med       Date:  2011-05-17       Impact factor: 5.531

Review 8.  Zebrafish models flex their muscles to shed light on muscular dystrophies.

Authors:  Joachim Berger; Peter D Currie
Journal:  Dis Model Mech       Date:  2012-11       Impact factor: 5.758

9.  Novel compounds for the treatment of Duchenne muscular dystrophy: emerging therapeutic agents.

Authors:  Steve D Wilton; Sue Fletcher
Journal:  Appl Clin Genet       Date:  2011-03-10

10.  Treatment of facioscapulohumeral muscular dystrophy with Denosumab.

Authors:  Stanley S Lefkowitz; Doris L Lefkowitz; Jeremy Kethley
Journal:  Am J Case Rep       Date:  2012-05-16
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