Zobrazeno 1 - 6
of 6
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc0568165009f65462f8ca63eb8c5e9
https://doi.org/10.1080/10715762.2022.2146501
https://doi.org/10.1080/10715762.2022.2146501
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630ecaf5141f8b7eeee06a1ea0bd12d5
https://pubmed.ncbi.nlm.nih.gov/2123980
https://pubmed.ncbi.nlm.nih.gov/2123980
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b31ed9631b345035e5e6f266b51901b5
https://pubmed.ncbi.nlm.nih.gov/3201231
https://pubmed.ncbi.nlm.nih.gov/3201231
Autor:
ANGELA M. S. LEZZA
Publikováno v:
Nature. 331(6152)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ebc6e2c2612a453002314b630c24961
https://pubmed.ncbi.nlm.nih.gov/3340155
https://pubmed.ncbi.nlm.nih.gov/3340155