Decreased Left Ventricular Ejection Fraction in Transgenic Mice Expressing Mutant Cardiac Troponin T-Q⁹², Responsible for Human Hypertrophic Cardiomyopathy

By Lim D-S.   Oberst L.   McCluggage M.   Youker K.   Lacy J.   deMayo F.   Entman M.L.   Roberts R.   Michael L.H.   Marian A.J.  

Journal of Molecular and Cellular Cardiology, Vol. 32, Iss. 3, 2000-03 ,pp. : 365-374

Academic Press

Access to resources Recommend Favorite

A specific mitochondrial DNA deletion (mtDNA 4977 ) is identified in a pedigree of a family with hearing loss

By Bai U.   Seidman M.D.  

Hearing Research, Vol. 154, Iss. 1, 2001-04 ,pp. : 73-80

Elsevier

Access to resources Recommend Favorite

Advances in Human Mitochondrial Diseases - Molecular Genetic Analysis of Pathogenic mtDNA Mutations

By Davidson E.   King M.P.  

Trends in Cardiovascular Medicine, Vol. 7, Iss. 1, 1997-01 ,pp. : 16-24

Elsevier

Access to resources Recommend Favorite

mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish

By Ross O.A.   McCormack R.   Maxwell L.D.   Duguid R.A.   Quinn D.J.   Barnett Y.A.   Rea I.M.   El-Agnaf O.M.A.   Gibson J.M.   Wallace A.   Middleton D.   Curran M.D.  

Experimental Gerontology, Vol. 38, Iss. 4, 2003-04 ,pp. : 397-405

Elsevier

Access to resources Recommend Favorite

Role of mtDNA lesions in anthracycline cardiotoxicity

By Lebrecht Dirk   Walker Ulrich  

Cardiovascular Toxicology, Vol. 7, Iss. 2, 2007-06 ,pp. : 108-113

Humana Press, Inc

Access to resources Recommend Favorite