pubmed-article:12134142 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0018787 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0070876 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0449258 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0596988 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C1524066 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0205191 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:12134142 | lifeskim:mentions | umls-concept:C0301625 | lld:lifeskim |
pubmed-article:12134142 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:12134142 | pubmed:dateCreated | 2002-8-1 | lld:pubmed |
pubmed-article:12134142 | pubmed:abstractText | The feasibility of gene therapy for cardiomyopathy, heart failure and other chronic cardiac muscle diseases is so far unproven. Here, we developed an in vivo recombinant adeno-associated virus (rAAV) transcoronary delivery system that allows stable, high efficiency and relatively cardiac-selective gene expression. We used rAAV to express a pseudophosphorylated mutant of human phospholamban (PLN), a key regulator of cardiac sarcoplasmic reticulum (SR) Ca(2+) cycling in BIO14.6 cardiomyopathic hamsters. The rAAV/S16EPLN treatment enhanced myocardial SR Ca(2+) uptake and suppressed progressive impairment of left ventricular (LV) systolic function and contractility for 28-30 weeks, thereby protecting cardiac myocytes from cytopathic plasma-membrane disruption. Low LV systolic pressure and deterioration in LV relaxation were also largely prevented by rAAV/S16EPLN treatment. Thus, transcoronary gene transfer of S16EPLN via rAAV vector is a potential therapy for progressive dilated cardiomyopathy and associated heart failure. | lld:pubmed |
pubmed-article:12134142 | pubmed:language | eng | lld:pubmed |
pubmed-article:12134142 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12134142 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12134142 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12134142 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12134142 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12134142 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12134142 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12134142 | pubmed:month | Aug | lld:pubmed |
pubmed-article:12134142 | pubmed:issn | 1078-8956 | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:GuYusuY | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:RossJohnJJr | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:WilsonJames... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:ChienKenneth... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:IkedaYasuhiro... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:IwanagaYoshit... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:MinamisawaSus... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:HoshijimaMasa... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:WangYibinY | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:WangLiliL | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:DateMoto-oMO | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:IwatateMitsuo... | lld:pubmed |
pubmed-article:12134142 | pubmed:author | pubmed-author:LiManxiangM | lld:pubmed |
pubmed-article:12134142 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12134142 | pubmed:volume | 8 | lld:pubmed |
pubmed-article:12134142 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12134142 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12134142 | pubmed:pagination | 864-71 | lld:pubmed |
pubmed-article:12134142 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:12134142 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:12134142 | pubmed:articleTitle | Chronic suppression of heart-failure progression by a pseudophosphorylated mutant of phospholamban via in vivo cardiac rAAV gene delivery. | lld:pubmed |
pubmed-article:12134142 | pubmed:affiliation | University of California, San Diego Institute of Molecular Medicine, La Jolla, California, USA. | lld:pubmed |
pubmed-article:12134142 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12134142 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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