Literature DB >> 22172418

Nemaline myopathies.

Carina Wallgren-Pettersson1, Caroline A Sewry, Kristen J Nowak, Nigel G Laing.   

Abstract

Nemaline myopathy constitutes a continuous spectrum of primary skeletal muscle disorders named after the Greek word for thread, nema. The diagnosis is based on muscle weakness, combined with visualization of nemaline bodies on muscle biopsy. The patients' muscle weakness is usually generalized, but there may be a selective pattern of more pronounced weakness, and, most importantly, respiratory muscles may be especially weak. Histologically, additional features may coexist with the nemaline bodies. There are 7 known causative genes. The function of the most recently identified gene is unknown, but the other 6 encoded proteins are associated with the muscle thin filament. The 2 most common causes of nemaline myopathy are recessive mutations in nebulin and de novo dominant mutations in skeletal muscle α-actin. At least 1 further gene remains to be identified. Patient care is based on managing the clinical symptoms. Animal models are helping to gain insight into pathogenesis, and a variety of therapeutic approaches are being investigated.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22172418     DOI: 10.1016/j.spen.2011.10.004

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  56 in total

1.  Treatment with ActRIIB-mFc Produces Myofiber Growth and Improves Lifespan in the Acta1 H40Y Murine Model of Nemaline Myopathy.

Authors:  Jennifer Tinklenberg; Hui Meng; Lin Yang; Fujun Liu; Raymond G Hoffmann; Mahua Dasgupta; Kenneth P Allen; Alan H Beggs; Edna C Hardeman; R Scott Pearsall; Robert H Fitts; Michael W Lawlor
Journal:  Am J Pathol       Date:  2016-04-18       Impact factor: 4.307

Review 2.  Targeting the sarcomere to correct muscle function.

Authors:  Peter M Hwang; Brian D Sykes
Journal:  Nat Rev Drug Discov       Date:  2015-04-17       Impact factor: 84.694

3.  A transcriptomics resource reveals a transcriptional transition during ordered sarcomere morphogenesis in flight muscle.

Authors:  Maria L Spletter; Christiane Barz; Assa Yeroslaviz; Xu Zhang; Sandra B Lemke; Adrien Bonnard; Erich Brunner; Giovanni Cardone; Konrad Basler; Bianca H Habermann; Frank Schnorrer
Journal:  Elife       Date:  2018-05-30       Impact factor: 8.140

4.  Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores.

Authors:  Karen Majczenko; Ann E Davidson; Sandra Camelo-Piragua; Pankaj B Agrawal; Richard A Manfready; Xingli Li; Sucheta Joshi; Jishu Xu; Weiping Peng; Alan H Beggs; Jun Z Li; Margit Burmeister; James J Dowling
Journal:  Am J Hum Genet       Date:  2012-07-19       Impact factor: 11.025

5.  A Zebrafish Model for a Human Myopathy Associated with Mutation of the Unconventional Myosin MYO18B.

Authors:  Ritika Gurung; Yosuke Ono; Sarah Baxendale; Samantha Lin Chiou Lee; Steven Moore; Meredith Calvert; Philip W Ingham
Journal:  Genetics       Date:  2016-11-22       Impact factor: 4.562

Review 6.  The makings of the 'actin code': regulation of actin's biological function at the amino acid and nucleotide level.

Authors:  Pavan Vedula; Anna Kashina
Journal:  J Cell Sci       Date:  2018-05-08       Impact factor: 5.285

7.  Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice.

Authors:  Jennifer A Tinklenberg; Emily M Siebers; Margaret J Beatka; Hui Meng; Lin Yang; Zizhao Zhang; Jacob A Ross; Julien Ochala; Carl Morris; Jane M Owens; Nigel G Laing; Kristen J Nowak; Michael W Lawlor
Journal:  Hum Mol Genet       Date:  2018-02-15       Impact factor: 6.150

8.  Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.

Authors:  Anne Guimier; Christopher T Gordon; François Godard; Gianina Ravenscroft; Myriam Oufadem; Christelle Vasnier; Caroline Rambaud; Patrick Nitschke; Christine Bole-Feysot; Cécile Masson; Stéphane Dauger; Cheryl Longman; Nigel G Laing; Béatrice Kugener; Damien Bonnet; Patrice Bouvagnet; Sylvie Di Filippo; Vincent Probst; Richard Redon; Philippe Charron; Agnès Rötig; Stanislas Lyonnet; Alain Dautant; Loïc de Pontual; Jean-Paul di Rago; Agnès Delahodde; Jeanne Amiel
Journal:  Am J Hum Genet       Date:  2016-08-11       Impact factor: 11.025

9.  KLHL40 deficiency destabilizes thin filament proteins and promotes nemaline myopathy.

Authors:  Ankit Garg; Jason O'Rourke; Chengzu Long; Jonathan Doering; Gianina Ravenscroft; Svetlana Bezprozvannaya; Benjamin R Nelson; Nadine Beetz; Lin Li; She Chen; Nigel G Laing; Robert W Grange; Rhonda Bassel-Duby; Eric N Olson
Journal:  J Clin Invest       Date:  2014-06-24       Impact factor: 14.808

10.  Muscle phenotypic variability in limb girdle muscular dystrophy 2 G.

Authors:  Julia F Paim; Ana Cotta; Antonio P Vargas; Monica M Navarro; Jaquelin Valicek; Elmano Carvalho; Antonio L da-Cunha; Estevão Plentz; Shelida V Braz; Reinaldo I Takata; Camila F Almeida; Mariz Vainzof
Journal:  J Mol Neurosci       Date:  2013-03-12       Impact factor: 3.444

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