Literature DB >> 17029922

Molecular biology of distal muscular dystrophies--sarcomeric proteins on top.

Bjarne Udd1.   

Abstract

During the last 10 years several muscular dystrophies within the group of distal myopathies have been clarified as to the molecular genetic cause of the disease. Currently, the next steps are carried out to identify the molecular pathogenesis downstream of the gene defects. Some early ideas on what is going on in the muscle cells based on the defect proteins are emerging. However, in no single distal muscular dystrophy these efforts have yet reached the point where direct trials for therapy would have been launched, and in many distal dystrophies the causative gene is still lacking. When comparing the gene defects in the distal dystrophies with the more common proximal muscular dystrophies such as dystrophinopathies or limb-girdle muscular dystrophies, there is a striking difference: the genes for distal dystrophies encode sarcomere proteins whereas the genes for proximal dystrophies more often encode sarcolemmal proteins.

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Year:  2006        PMID: 17029922     DOI: 10.1016/j.bbadis.2006.08.005

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

Review 1.  Muscle giants: molecular scaffolds in sarcomerogenesis.

Authors:  Aikaterini Kontrogianni-Konstantopoulos; Maegen A Ackermann; Amber L Bowman; Solomon V Yap; Robert J Bloch
Journal:  Physiol Rev       Date:  2009-10       Impact factor: 37.312

2.  Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy.

Authors:  Roula Ghaoui; Johanna Palmio; Janice Brewer; Monkol Lek; Merrilee Needham; Anni Evilä; Peter Hackman; Per-Harald Jonson; Sini Penttilä; Anna Vihola; Sanna Huovinen; Mikaela Lindfors; Ryan L Davis; Leigh Waddell; Simran Kaur; Con Yiannikas; Kathryn North; Nigel Clarke; Daniel G MacArthur; Carolyn M Sue; Bjarne Udd
Journal:  Neurology       Date:  2015-12-30       Impact factor: 9.910

3.  A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.

Authors:  Stojan Perić; Jelena Nikodinović Glumac; Ana Töpf; Dušanka Savić-Pavićević; Lauren Phillips; Katherine Johnson; Marcus Cassop-Thompson; Liwen Xu; Marta Bertoli; Monkol Lek; Daniel MacArthur; Miloš Brkušanin; Sanja Milenković; Vedrana Milić Rašić; Bojan Banko; Ružica Maksimović; Hanns Lochmüller; Vidosava Rakočević Stojanović; Volker Straub
Journal:  Eur J Hum Genet       Date:  2017-03-15       Impact factor: 4.246

4.  Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy.

Authors:  Sebahattin Cirak; Florian von Deimling; Shrikesh Sachdev; Wesley J Errington; Ralf Herrmann; Carsten Bönnemann; Knut Brockmann; Stephan Hinderlich; Tom H Lindner; Alice Steinbrecher; Katrin Hoffmann; Gilbert G Privé; Mark Hannink; Peter Nürnberg; Thomas Voit
Journal:  Brain       Date:  2010-06-16       Impact factor: 13.501

5.  Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.

Authors:  Jan Senderek; Sean M Garvey; Michael Krieger; Velina Guergueltcheva; Andoni Urtizberea; Andreas Roos; Miriam Elbracht; Claudia Stendel; Ivailo Tournev; Violeta Mihailova; Howard Feit; Jeff Tramonte; Peter Hedera; Kristy Crooks; Carsten Bergmann; Sabine Rudnik-Schöneborn; Klaus Zerres; Hanns Lochmüller; Eric Seboun; Joachim Weis; Jacques S Beckmann; Michael A Hauser; Charles E Jackson
Journal:  Am J Hum Genet       Date:  2009-04-02       Impact factor: 11.025

6.  Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.

Authors:  Montse Olivé; Alexey Shatunov; Laura Gonzalez; Olga Carmona; Dolores Moreno; Lidia Gonzalez Quereda; J A Martinez-Matos; Lev G Goldfarb; Isidro Ferrer
Journal:  Neuromuscul Disord       Date:  2008-10-22       Impact factor: 4.296

7.  [Myofibrillary myopathy due to the ZASP mutation Ala147Thr : two cases with exclusively distal leg involvement].

Authors:  T Kraya; W Kress; D Stoevesant; M Deschauer; S Zierz
Journal:  Nervenarzt       Date:  2013-02       Impact factor: 1.214

8.  Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy.

Authors:  Rachael M Duff; Valerie Tay; Peter Hackman; Gianina Ravenscroft; Catriona McLean; Paul Kennedy; Alina Steinbach; Wiebke Schöffler; Peter F M van der Ven; Dieter O Fürst; Jaeguen Song; Kristina Djinović-Carugo; Sini Penttilä; Olayinka Raheem; Katrina Reardon; Alessandro Malandrini; Simona Gambelli; Marcello Villanova; Kristen J Nowak; David R Williams; John E Landers; Robert H Brown; Bjarne Udd; Nigel G Laing
Journal:  Am J Hum Genet       Date:  2011-05-27       Impact factor: 11.025

9.  Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population.

Authors:  Fiona L M Norwood; Chris Harling; Patrick F Chinnery; Michelle Eagle; Kate Bushby; Volker Straub
Journal:  Brain       Date:  2009-09-18       Impact factor: 13.501

10.  Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features--a case report.

Authors:  Guja Astrea; Antonio Petrucci; Denise Cassandrini; Marco Savarese; Rosanna Trovato; Ludovico Lispi; Anna Rubegni; Manlio Giacanelli; Roberto Massa; Vincenzo Nigro; Filippo M Santorelli
Journal:  BMC Med Genet       Date:  2016-03-22       Impact factor: 2.103

  10 in total

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