Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies.
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| Title: | Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. |
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| Authors: | Bachinski LL; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Baggerly KA; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Neubauer VL; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Nixon TJ; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Raheem O; Department of Neurology, Tampere University Hospital and Medical School, Tampere, Finland., Sirito M; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Unruh AK; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Zhang J; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Nagarajan L; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Timchenko LT; Department of Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX, USA., Bassez G; Neuromuscular Reference Center, Henri Mondor University Hospital, INSERM U955, East-Paris University, Créteil, France., Eymard B; Reference Center for Neuromuscular Diseases, Institute of Myology, Pitié-Salpêtrière Hospital, Paris, France., Gamez J; Neuromuscular Disorders Clinic, Neurology Department, Hospital General Vall d'Hebron, Barcelona, Spain., Ashizawa T; Department of Neurology, McKnight Brain Institute, University of Florida, Gainesville, FL, USA., Mendell JR; Division of Child Neurology, Nationwide Childrens Hospital, Ohio State University College of Medicine, Columbus, OH, USA., Udd B; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Folkhälsan Institute of Genetics and Department of Medical Genetics, University of Helsinki, Finland; Department of Neurology, Vasa Central Hospital, Finland., Krahe R; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Graduate Programs in Human & Molecular Genetics, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA; Graduate Programs in Genes & Development, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA. Electronic address: rkrahe@mdanderson.org. |
| Source: | Neuromuscular disorders : NMD [Neuromuscul Disord] 2014 Mar; Vol. 24 (3), pp. 227-40. Date of Electronic Publication: 2013 Nov 15. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Pergamon Press Country of Publication: England NLM ID: 9111470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2364 (Electronic) Linking ISSN: 09608966 NLM ISO Abbreviation: Neuromuscul Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 24332166 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Bachinski+LL%22">Bachinski LL</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Baggerly+KA%22">Baggerly KA</searchLink>; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Neubauer+VL%22">Neubauer VL</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Nixon+TJ%22">Nixon TJ</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Raheem+O%22">Raheem O</searchLink>; Department of Neurology, Tampere University Hospital and Medical School, Tampere, Finland.<br /><searchLink fieldCode="AU" term="%22Sirito+M%22">Sirito M</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Unruh+AK%22">Unruh AK</searchLink>; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Zhang+J%22">Zhang J</searchLink>; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Nagarajan+L%22">Nagarajan L</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Timchenko+LT%22">Timchenko LT</searchLink>; Department of Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Bassez+G%22">Bassez G</searchLink>; Neuromuscular Reference Center, Henri Mondor University Hospital, INSERM U955, East-Paris University, Créteil, France.<br /><searchLink fieldCode="AU" term="%22Eymard+B%22">Eymard B</searchLink>; Reference Center for Neuromuscular Diseases, Institute of Myology, Pitié-Salpêtrière Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Gamez+J%22">Gamez J</searchLink>; Neuromuscular Disorders Clinic, Neurology Department, Hospital General Vall d'Hebron, Barcelona, Spain.<br /><searchLink fieldCode="AU" term="%22Ashizawa+T%22">Ashizawa T</searchLink>; Department of Neurology, McKnight Brain Institute, University of Florida, Gainesville, FL, USA.<br /><searchLink fieldCode="AU" term="%22Mendell+JR%22">Mendell JR</searchLink>; Division of Child Neurology, Nationwide Childrens Hospital, Ohio State University College of Medicine, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Udd+B%22">Udd B</searchLink>; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Folkhälsan Institute of Genetics and Department of Medical Genetics, University of Helsinki, Finland; Department of Neurology, Vasa Central Hospital, Finland.<br /><searchLink fieldCode="AU" term="%22Krahe+R%22">Krahe R</searchLink>; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Graduate Programs in Human & Molecular Genetics, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA; Graduate Programs in Genes & Development, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA. Electronic address: rkrahe@mdanderson.org. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229111470%22">Neuromuscular disorders : NMD</searchLink> [Neuromuscul Disord] 2014 Mar; Vol. 24 (3), pp. 227-40. <i>Date of Electronic Publication: </i>2013 Nov 15. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Pergamon+Press%22">Pergamon Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9111470 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1873-2364 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209608966%22">09608966 </searchLink><i>NLM ISO Abbreviation: </i>Neuromuscul Disord <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=24332166 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2013.11.001 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 227 Titles: – TitleFull: Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bachinski LL – PersonEntity: Name: NameFull: Baggerly KA – PersonEntity: Name: NameFull: Neubauer VL – PersonEntity: Name: NameFull: Nixon TJ – PersonEntity: Name: NameFull: Raheem O – PersonEntity: Name: NameFull: Sirito M – PersonEntity: Name: NameFull: Unruh AK – PersonEntity: Name: NameFull: Zhang J – PersonEntity: Name: NameFull: Nagarajan L – PersonEntity: Name: NameFull: Timchenko LT – PersonEntity: Name: NameFull: Bassez G – PersonEntity: Name: NameFull: Eymard B – PersonEntity: Name: NameFull: Gamez J – PersonEntity: Name: NameFull: Ashizawa T – PersonEntity: Name: NameFull: Mendell JR – PersonEntity: Name: NameFull: Udd B – PersonEntity: Name: NameFull: Krahe R IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2014 Mar Type: published Y: 2014 Identifiers: – Type: issn-electronic Value: 1873-2364 Numbering: – Type: volume Value: 24 – Type: issue Value: 3 Titles: – TitleFull: Neuromuscular disorders : NMD Type: main |
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