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Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathwa...

Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathwa...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_19459645

Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2

About this item

Full title

Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2

Publisher

Elmsford, NY: Cognizant Communication Corporation

Journal title

Gene expression, 2007-01, Vol.13 (6), p.339-351

Language

English

Formats

Publication information

Publisher

Elmsford, NY: Cognizant Communication Corporation

More information

Scope and Contents

Contents

An RNA gain-of-function of expanded transcripts is the most accredited molecular mechanism for myotonic dystrophy type 1 (DM1) and 2 (DM2). To disclose molecular parallels and divergences in pathogenesis of both disorders, we compared the expression profile of muscle biopsies from DM1
and DM2 patients to controls. DM muscle tissues showed a redu...

Alternative Titles

Full title

Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_19459645

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_19459645

Other Identifiers

ISSN

1052-2166

E-ISSN

1555-3884

DOI

10.3727/000000006781510705

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