Transgenic Mice Overexpressing MutantPRKAG2Define the Cause of Wolff-Parkinson-White Syndrome in Glycogen Storage Cardiomyopathy-Reference-Cited by-同舟云学术

Transgenic Mice Overexpressing MutantPRKAG2Define the Cause of Wolff-Parkinson-White Syndrome in Glycogen Storage Cardiomyopathy

Published:2003-06-10 Issue:22 Volume:107 Page:2850-2856
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Arad Michael¹,Moskowitz Ivan P.¹,Patel Vickas V.¹,Ahmad Ferhaan¹,Perez-Atayde Antonio R.¹,Sawyer Douglas B.¹,Walter Mark¹,Li Guo H.¹,Burgon Patrick G.¹,Maguire Colin T.¹,Stapleton David¹,Schmitt Joachim P.¹,Guo X.X.¹,Pizard Anne¹,Kupershmidt Sabina¹,Roden Dan M.¹,Berul Charles I.¹,Seidman Christine E.¹,Seidman J.G.¹

Affiliation:

1. From the Department of Genetics, Harvard Medical School and Howard Hughes Medical Institute (M.A., I.P.M., F.A., G.H.L., P.G.B., J.P.S., A.P., C.E.S., J.G.S.), the Department of Pathology and Cardiac Registry, Children’s Hospital, and Harvard Medical School (I.P.M., A.R.P.-A.), the Department of Cardiology, Children’s Hospital and Department of Pediatrics, Harvard Medical School (V.V.P., C.T.M., C.I.B.), Boston University Medical Center, Myocardial Biology Unit (D.B.S., X.X.G.), and the Division of...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference29 articles.

1. Dealing with energy demand: the AMP-activated protein kinase

2. Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

3. Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

4. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

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