Coordinate induction of AMP deaminase in human atrium with mitochondrial DNA deletion.
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M. Shimoyama | I. Hisatome | T. Morisaki | H. Morisaki | M. Kitakaze | E. Nanba | G. Shiota | Yasutaka Yamamoto | K. Ogino | C. Shigemasa | O. Igawa | M. Yamawaki | S. Ishiguro | S. Ohgi | N. Sasaki | M. Tsuboi | Y. Tomikura
[1] M. Shimoyama,et al. Mitochondrial DNA deletion associated with the reduction of adenine nucleotides in human atrium and atrial fibrillation , 2001, European journal of clinical investigation.
[2] J. V. van Beek,et al. Increased hypoxic stress decreases AMP hydrolysis in rabbit heart. , 1999, Cardiovascular research.
[3] Douglas C. Wallace,et al. Coordinate Induction of Energy Gene Expression in Tissues of Mitochondrial Disease Patients* , 1999, The Journal of Biological Chemistry.
[4] M. Hori,et al. α1-Adrenoceptor Activation Increases Ecto-5′-Nucleotidase Activity and Adenosine Release in Rat Cardiomyocytes by Activating Protein Kinase C , 1995 .
[5] K. Majamaa,et al. Mitochondrial DNA deletion diagnosed by analysis of an endomyocardial biopsy specimen from a patient with Kearns-Sayre syndrome and complete heart block , 1992, British heart journal.
[6] T. Ozawa,et al. Quantitative analysis of age-associated accumulation of mitochondrial DNA with deletion in human hearts. , 1991, Biochemical and biophysical research communications.
[7] D. Wallace,et al. Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease. , 1991, JAMA.
[8] T. Ozawa,et al. Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia. , 1991, American heart journal.
[9] T. Ozawa,et al. Mitochondrial DNA deletions in inherited recurrent myoglobinuria , 1991, Annals of neurology.
[10] K. Ohno,et al. Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence. , 1990, Biochemical and biophysical research communications.
[11] I. Fox,et al. Isocratic separation of ATP and its degradation products from biological fluids by automated liquid chromatography. , 1988, Clinical chemistry.
[12] M. Brooke,et al. Myoadenylate Deaminase Deficiency , 1983 .
[13] T. Watanabe,et al. Distribution of AMP-deaminase isozymes in rat tissues. , 1978, European journal of biochemistry.
[14] H. Urschel,et al. Serum 5′‐nucleotidase in patients with tumor in the liver , 1966, Cancer.
[15] Charles R.scriver. The Metabolic basis of inherited disease , 1989 .