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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1988 2
1989 2
1990 2
1991 1
1993 2
1994 1
1996 4
1997 2
1998 3
1999 6
2000 2
2001 4
2002 1
2003 1
2004 3
2005 1
2006 1
2008 3
2009 3
2010 1
2011 1
2012 2
2013 1
2015 3
2016 3
2017 1
2019 1
2020 2
2021 3
2022 3
2023 3
2024 0

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65 results

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Page 1
The Biochemistry and Physiology of Mitochondrial Fatty Acid beta-Oxidation and Its Genetic Disorders.
Houten SM, Violante S, Ventura FV, Wanders RJ. Houten SM, et al. Annu Rev Physiol. 2016;78:23-44. doi: 10.1146/annurev-physiol-021115-105045. Epub 2015 Oct 14. Annu Rev Physiol. 2016. PMID: 26474213 Review.
Mitochondrial fatty acid beta-oxidation (FAO) is the major pathway for the degradation of fatty acids and is essential for maintaining energy homeostasis in the human body. ...But even when glucose is abundantly available, FAO is a main energy source for the heart, skeleta …
Mitochondrial fatty acid beta-oxidation (FAO) is the major pathway for the degradation of fatty acids and is essential for maintainin …
Carnitine transport and fatty acid oxidation.
Longo N, Frigeni M, Pasquali M. Longo N, et al. Biochim Biophys Acta. 2016 Oct;1863(10):2422-35. doi: 10.1016/j.bbamcr.2016.01.023. Epub 2016 Jan 29. Biochim Biophys Acta. 2016. PMID: 26828774 Free PMC article. Review.
Carnitine is essential for the transfer of long-chain fatty acids across the inner mitochondrial membrane for subsequent beta-oxidation. It can be synthesized by the body or assumed with the diet from meat and dairy products. ...Carnitine is accumulated by the cells …
Carnitine is essential for the transfer of long-chain fatty acids across the inner mitochondrial membrane for subsequent beta- …
Mitochondrial cytopathies.
El-Hattab AW, Scaglia F. El-Hattab AW, et al. Cell Calcium. 2016 Sep;60(3):199-206. doi: 10.1016/j.ceca.2016.03.003. Epub 2016 Mar 4. Cell Calcium. 2016. PMID: 26996063 Review.
Mitochondria are found in all nucleated human cells and perform a variety of essential functions, including the generation of cellular energy. Most of mitochondrial proteins are encoded by the nuclear DNA (nDNA) whereas a very small fraction is encoded by the mit …
Mitochondria are found in all nucleated human cells and perform a variety of essential functions, including the generation of cellular energ …
Mitochondrial myopathies.
DiMauro S. DiMauro S. Curr Opin Rheumatol. 2006 Nov;18(6):636-41. doi: 10.1097/01.bor.0000245729.17759.f2. Curr Opin Rheumatol. 2006. PMID: 17053512 Review.
Barth syndrome, an X-linked recessive mitochondrial myopathy/cardiopathy, is associated with decreased amount and altered structure of cardiolipin, the main phospholipid of the inner mitochondrial membrane, but a secondary impairment of respiratory cha …
Barth syndrome, an X-linked recessive mitochondrial myopathy/cardiopathy, is associated with decreased amount and altered stru …
Mitochondriopathies.
Finsterer J. Finsterer J. Eur J Neurol. 2004 Mar;11(3):163-86. doi: 10.1046/j.1351-5101.2003.00728.x. Eur J Neurol. 2004. PMID: 15009163 Review.
Mitochondriopathies (MCPs) are either due to sporadic or inherited mutations in nuclear or mitochondrial DNA located genes (primary MCPs), or due to exogenous factors (secondary MCPs). MCPs usually show a chronic, slowly progressive course and present with multiorgan invol …
Mitochondriopathies (MCPs) are either due to sporadic or inherited mutations in nuclear or mitochondrial DNA located genes (primary M …
Oxidative stress, mitochondrial dysfunction, and respiratory chain enzyme defects in inflammatory myopathies.
Danieli MG, Antonelli E, Piga MA, Cozzi MF, Allegra A, Gangemi S. Danieli MG, et al. Autoimmun Rev. 2023 May;22(5):103308. doi: 10.1016/j.autrev.2023.103308. Epub 2023 Feb 21. Autoimmun Rev. 2023. PMID: 36822387 Free article. Review.
We investigated the relationship between oxidative stress and inflammatory myopathies. We searched in the current literature the role of mitochondria and respiratory chain defects as sources of oxidative stress and reactive oxygen species production that led to musc …
We investigated the relationship between oxidative stress and inflammatory myopathies. We searched in the current literature the role …
Mitochondrial encephalomyopathies.
DiMauro S, Moraes CT. DiMauro S, et al. Arch Neurol. 1993 Nov;50(11):1197-208. doi: 10.1001/archneur.1993.00540110075008. Arch Neurol. 1993. PMID: 8215979 Review.
The vast majority of mitochondrial proteins are encoded by nuclear DNA (nDNA) and have to be imported from the cytoplasm into mitochondria through a complex translocation machinery, which is also under the control of the nuclear genome. In addition, nDNA encodes sev …
The vast majority of mitochondrial proteins are encoded by nuclear DNA (nDNA) and have to be imported from the cytoplasm into …
Mitochondrial encephalomyopathies.
Lombes A, Bonilla E, Dimauro S. Lombes A, et al. Rev Neurol (Paris). 1989;145(10):671-89. Rev Neurol (Paris). 1989. PMID: 2682927 Review.
This clinical, histological and biochemical triad led to the definition of mitochondrial myopathies. Subsequently, the triad was seldom encountered, and most mitochondrial myopathies were primarily defined by the presence of morphological abnormalit …
This clinical, histological and biochemical triad led to the definition of mitochondrial myopathies. Subsequently, the triad w …
Mitochondrial Mutations Can Alter Neuromuscular Transmission in Congenital Myasthenic Syndrome and Mitochondrial Disease.
O'Connor K, Spendiff S, Lochmüller H, Horvath R. O'Connor K, et al. Int J Mol Sci. 2023 May 9;24(10):8505. doi: 10.3390/ijms24108505. Int J Mol Sci. 2023. PMID: 37239850 Free PMC article. Review.
Mitochondrial disease and CMS can present with similar symptoms, and potentially one in four patients with mitochondrial myopathy exhibit NMJ defects. This review highlights research indicating the prominent roles of mitochondria at both the pre- and p …
Mitochondrial disease and CMS can present with similar symptoms, and potentially one in four patients with mitochondrial my …
Mechano-energetic aspects of Barth syndrome.
Dudek J, Maack C. Dudek J, et al. J Inherit Metab Dis. 2022 Jan;45(1):82-98. doi: 10.1002/jimd.12427. Epub 2021 Sep 9. J Inherit Metab Dis. 2022. PMID: 34423473 Review.
Oxidative phosphorylation is governed by the respiratory chain located in the inner mitochondrial membrane. The inner mitochondrial membrane is the only cellular membrane with significant amounts of the phospholipid cardiolipin, and cardiolipin …
Oxidative phosphorylation is governed by the respiratory chain located in the inner mitochondrial membrane. The inner mitoc …
65 results