Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Angela M S Lezza"'
Autor:
Maria Tolomeo, Guglielmina Chimienti, Martina Lanza, Roberto Barbaro, Alessia Nisco, Tiziana Latronico, Piero Leone, Giuseppe Petrosillo, Grazia Maria Liuzzi, Bryony Ryder, Michal Inbar-Feigenberg, Matilde Colella, Angela M. S. Lezza, Rikke K. J. Olsen, Maria Barile
Publikováno v:
Free Radical Research. 56:511-525
Autor:
Anna Picca, Vito Pesce, Flavio Fracasso, Anna-Maria Joseph, Christiaan Leeuwenburgh, Angela M S Lezza
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74644 (2013)
Aging affects mitochondria in a tissue-specific manner. Calorie restriction (CR) is, so far, the only intervention able to delay or prevent the onset of several age-related changes also in mitochondria. Using livers from middle age (18-month-old), 28
Externí odkaz:
https://doaj.org/article/dcf216fefc904046a9ee8b94673c9811
Autor:
Jinze Xu, Arnold Y Seo, Darya A Vorobyeva, Christy S Carter, Stephen D Anton, Angela M S Lezza, Christiaan Leeuwenburgh
Publikováno v:
PLoS ONE, Vol 5, Iss 5, p e10572 (2010)
Mitochondrial dysfunction and oxidative stress are central mechanisms underlying the aging process and the pathogenesis of many age-related diseases. Selected antioxidants and specific combinations of nutritional compounds could target many biochemic
Externí odkaz:
https://doaj.org/article/00739586069b480c9b8cfabc5b0ab001
Autor:
John M. Shoffner, Marie T. Lott, Peter Seibel, Angela M. S. Lezza, Douglas C. Wallace, Alexander S. Voljavec
Publikováno v:
Pediatric research. 28(5)
A number of neuromuscular diseases are associated with molecular defects in the mitochondrial DNA (mtDNA). These include: 1) a missense mutation at nucleotide 11778 in the mtDNA of Leber's hereditary optic neuropathy patients; 2) a heterogeneous arra
Autor:
Angela M. S. Lezza, Gurparkash Singh, Eeva K. Nikoskelainen, Louis J. Elsas, Judy A. Hodge, Douglas C. Wallace, Theodore G. Schurr, Marie T. Lott
Publikováno v:
Science (New York, N.Y.). 242(4884)
Leber's hereditary optic neuropathy is a maternally inherited disease resulting in optic nerve degeneration and cardiac dysrhythmia. A mitochondrial DNA replacement mutation was identified that correlated with this disease in multiple families. This
Autor:
ANGELA M. S. LEZZA
Publikováno v:
Nature. 331(6152)
Autor:
Tolomeo, Maria1,2 (AUTHOR), Chimienti, Guglielmina1 (AUTHOR), Lanza, Martina1 (AUTHOR), Barbaro, Roberto1 (AUTHOR), Nisco, Alessia1 (AUTHOR), Latronico, Tiziana1 (AUTHOR), Leone, Piero1 (AUTHOR), Petrosillo, Giuseppe3 (AUTHOR), Liuzzi, Grazia Maria1 (AUTHOR), Ryder, Bryony4 (AUTHOR), Inbar-Feigenberg, Michal5 (AUTHOR), Colella, Matilde1 (AUTHOR), Lezza, Angela M. S.1 (AUTHOR), Olsen, Rikke K. J.6 (AUTHOR), Barile, Maria1 (AUTHOR)
Publikováno v:
Free Radical Research. Jul/Aug2022, Vol. 56 Issue 7/8, p511-525. 15p. 2 Color Photographs, 3 Diagrams, 5 Graphs.
Autor:
Picca, Anna1,2, Riezzo, Giuseppe3, Lezza, Angela M. S.1, Clemente, Caterina3, Pesce, Vito1, Orlando, Antonella3, Chimienti, Guglielmina1, Russo, Francesco3 francesco.russo@irccsdebellis.it
Publikováno v:
European Journal of Clinical Investigation. Feb2018, Vol. 48 Issue 2, p1-1. 8p.
Autor:
Lezza, Angela
Publikováno v:
Frontiers in Biology; Feb2012, Vol. 7 Issue 1, p30-39, 10p
Autor:
Pesce, Vito, Cormio, Antonella, Fracasso, Flavio, Lezza, Angela M. S., Cantatore, Palmiro, Gadaleta, Maria Nicola, Smith, James R.
Publikováno v:
Journals of Gerontology Series A: Biological Sciences & Medical Sciences; Jun2005, Vol. 60 Issue 6, p715-723, 9p, 1 Diagram, 4 Graphs