Literature DB >> 19181102

Other model organisms for sarcomeric muscle diseases.

John Sparrow1, Simon M Hughes, Laurent Segalat.   

Abstract

Model organisms are vital to our understanding of human muscle biology and disease. The potential of the nematode Caenorhabditis elegans, the fruitfly, Drosophila melanogaster and the zebrafish, Danio rerio, as model genetic organisms for the study of human muscle disease is discussed by examining their muscle biology, muscle genetics and development. The powerful genetic tools available with each organism are outlined. It is concluded that these organisms have already demonstrated potential in facilitating the study of muscle disease and in screening for therapeutic agents.

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Year:  2008        PMID: 19181102      PMCID: PMC3360967          DOI: 10.1007/978-0-387-84847-1_14

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  103 in total

1.  Evolutionary origins of vertebrate appendicular muscle.

Authors:  C Neyt; K Jagla; C Thisse; B Thisse; L Haines; P D Currie
Journal:  Nature       Date:  2000-11-02       Impact factor: 49.962

2.  Transplanted primary neonatal myoblasts can give rise to functional satellite cells as identified using the Myf5nlacZl+ mouse.

Authors:  L Heslop; J R Beauchamp; S Tajbakhsh; M E Buckingham; T A Partridge; P S Zammit
Journal:  Gene Ther       Date:  2001-05       Impact factor: 5.250

3.  Distinct mechanisms regulate slow-muscle development.

Authors:  M J Barresi; J A D'Angelo; L P Hernández; S H Devoto
Journal:  Curr Biol       Date:  2001-09-18       Impact factor: 10.834

4.  A tropomyosin-2 mutation suppresses a troponin I myopathy in Drosophila.

Authors:  B Naimi; A Harrison; M Cummins; U Nongthomba; S Clark; I Canal; A Ferrus; J C Sparrow
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

5.  Muscular degeneration in the absence of dystrophin is a calcium-dependent process.

Authors:  M C Mariol; L Ségalat
Journal:  Curr Biol       Date:  2001-10-30       Impact factor: 10.834

6.  The dystrophin / utrophin homologues in Drosophila and in sea urchin.

Authors:  S Neuman; A Kaban; T Volk; D Yaffe; U Nudel
Journal:  Gene       Date:  2001-01-24       Impact factor: 3.688

7.  Expression and function of the Drosophila ACT88F actin isoform is not restricted to the indirect flight muscles.

Authors:  U Nongthomba; S Pasalodos-Sanchez; S Clark; J D Clayton; J C Sparrow
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

8.  Cardiac troponin T is essential in sarcomere assembly and cardiac contractility.

Authors:  Amy J Sehnert; Anja Huq; Brant M Weinstein; Charline Walker; Mark Fishman; Didier Y R Stainier
Journal:  Nat Genet       Date:  2002-04-22       Impact factor: 38.330

9.  Genetic evidence for a dystrophin-glycoprotein complex (DGC) in Caenorhabditis elegans.

Authors:  Karine Grisoni; Edwige Martin; Kathrin Gieseler; Marie-Christine Mariol; Laurent Ségalat
Journal:  Gene       Date:  2002-07-10       Impact factor: 3.688

Review 10.  Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

Authors:  Madeleine Durbeej; Kevin P Campbell
Journal:  Curr Opin Genet Dev       Date:  2002-06       Impact factor: 5.578

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  11 in total

Review 1.  Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine.

Authors:  Nalinda B Wasala; Shi-Jie Chen; Dongsheng Duan
Journal:  Expert Opin Drug Discov       Date:  2020-01-30       Impact factor: 6.098

2.  In vitro indeterminate teleost myogenesis appears to be dependent on Pax3.

Authors:  Jacob Michael Froehlich; Nicholas J Galt; Matthew J Charging; Ben M Meyer; Peggy R Biga
Journal:  In Vitro Cell Dev Biol Anim       Date:  2013-04-24       Impact factor: 2.416

3.  The systematic identification of cytoskeletal genes required for Drosophila melanogaster muscle maintenance.

Authors:  Alexander D Perkins; Michael J J Lee; Guy Tanentzapf
Journal:  Sci Data       Date:  2014-03-11       Impact factor: 6.444

Review 4.  Drosophila in the Heart of Understanding Cardiac Diseases: Modeling Channelopathies and Cardiomyopathies in the Fruitfly.

Authors:  Ouarda Taghli-Lamallem; Emilie Plantié; Krzysztof Jagla
Journal:  J Cardiovasc Dev Dis       Date:  2016-02-18

Review 5.  Molecular mechanisms of heart failure: insights from Drosophila.

Authors:  Shasha Zhu; Zhe Han; Yan Luo; Yulin Chen; Qun Zeng; Xiushan Wu; Wuzhou Yuan
Journal:  Heart Fail Rev       Date:  2017-01       Impact factor: 4.214

Review 6.  Non-coding RNAs in muscle differentiation and musculoskeletal disease.

Authors:  Monica Ballarino; Mariangela Morlando; Alessandro Fatica; Irene Bozzoni
Journal:  J Clin Invest       Date:  2016-06-01       Impact factor: 14.808

Review 7.  Integrated control of protein degradation in C. elegans muscle.

Authors:  Susann Lehmann; Freya Shephard; Lewis A Jacobson; Nathaniel J Szewczyk
Journal:  Worm       Date:  2012-07-01

8.  Knockdown of the C. elegans kinome identifies kinases required for normal protein homeostasis, mitochondrial network structure, and sarcomere structure in muscle.

Authors:  Susann Lehmann; Joseph J Bass; Nathaniel J Szewczyk
Journal:  Cell Commun Signal       Date:  2013-09-23       Impact factor: 5.712

9.  An ongoing role for structural sarcomeric components in maintaining Drosophila melanogaster muscle function and structure.

Authors:  Alexander D Perkins; Guy Tanentzapf
Journal:  PLoS One       Date:  2014-06-10       Impact factor: 3.240

10.  Overexpression of miRNA-9 Generates Muscle Hypercontraction Through Translational Repression of Troponin-T in Drosophila melanogaster Indirect Flight Muscles.

Authors:  Prasanna Katti; Divesh Thimmaya; Aditi Madan; Upendra Nongthomba
Journal:  G3 (Bethesda)       Date:  2017-10-05       Impact factor: 3.154

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